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        <title>Journal of neurosurgery. Pediatrics via MedWorm.com</title>
        <description>MedWorm.com provides a medical RSS filtering service. Over 6000 RSS medical sources are combined and output via different filters. This feed contains the latest items from the 'Journal of neurosurgery. Pediatrics' source.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=Journal+of+neurosurgery.+Pediatrics&t=Journal+of+neurosurgery.+Pediatrics&s=Search&f=source]]></link>
        <lastBuildDate>Sat, 10 Oct 2009 19:33:23 +0100</lastBuildDate>
        <item>
            <title>The pediatric neurosurgical workforce: defining the current supply. Clinical article.</title>
            <link>http://www.medworm.com/index.php?rid=2122658&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19119896%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: The authors estimate that there are fewer than 200 pediatric neurosurgeons currently practicing in the United States. Current practice patterns unique to pediatrics may have important implications in recruiting and retaining the next generation of pediatric neurosurgeons.
    PMID: 19119896 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2122658</comments>
            <pubDate>Thu, 01 Jan 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2122658</guid>        </item>
        <item>
            <title>Intraventricular baclofen for dystonia: techniques and outcomes. Clinical article.</title>
            <link>http://www.medworm.com/index.php?rid=2122657&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19119897%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: Intraventricular baclofen is an effective method of infusing baclofen to treat severe, generalized secondary dystonia, and, at times, heredodegenerative dystonia. The site of baclofen's activity when treating dystonia may be at the cortical level, and intraventricular infusion may result in higher baclofen concentrations over the cortex than intrathecal infusion. Additional studies are necessary to determine whether IVB is effective at lower doses than those used with intrathecal baclofen administration.
    PMID: 19119897 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2122657</comments>
            <pubDate>Thu, 01 Jan 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2122657</guid>        </item>
        <item>
            <title>Jefferson fractures of the immature spine. Report of 3 cases.</title>
            <link>http://www.medworm.com/index.php?rid=2122656&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19119898%26dopt%3DAbstract</link>
            <description>Authors: AuYong N, Piatt J
    Jefferson fractures of the immature spine have received little attention in the study of pediatric spinal trauma. Fractures through synchondroses are a possibility in the immature spine, in addition to fractures through osseous portions of the vertebral ring, and they create opportunities for misinterpretation of diagnostic imaging. The authors describe 3 examples of Jefferson fractures in young children. All 3 cases featured fractures through an anterior synchondrosis in association with persistence of the posterior synchondrosis or a fracture of the posterior arch. The possibility of a Jefferson fracture should be considered for any child presenting with neck pain, cervical muscle spasm, or torticollis following a head injury, despite a seemingly normal cer...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2122656</comments>
            <pubDate>Thu, 01 Jan 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2122656</guid>        </item>
        <item>
            <title>Computed tomography morphometric analysis for C-1 lateral mass screw placement in children. Clinical article.</title>
            <link>http://www.medworm.com/index.php?rid=2122655&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19119899%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: A significant variation in the morphological features of C-1 exists, especially between the left and right sides and in younger children. The differences between boys and girls are clinically insignificant. The critical measurement of whether the C-1 lateral mass in a child could accommodate a 3.5-mm-diameter screw is the width of the lateral mass and its proximity to the vertebral artery. Only 1 of 152 lateral masses studied would not have been able to accommodate a lateral mass screw. This study reemphasizes the importance of a preoperative CT scan of the upper cervical spine to assure safe and effective placement of the instrumentation at this level.
    PMID: 19119899 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2122655</comments>
            <pubDate>Thu, 01 Jan 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2122655</guid>        </item>
        <item>
            <title>Spinal congenital dermal sinus in a chick embryo model. Laboratory investigation.</title>
            <link>http://www.medworm.com/index.php?rid=2122654&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19119900%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: Implantation of donor amniotic tissue in the closing chick neural tube does result in a dimple, from which a strand of tissue continues to the neural tube in various cases, indicating that formation of a dermal sinus-like anomaly can be successfully induced by experimental continuation of the connection between neural tube and surface ectoderm. This finding strengthens the hypothesis that a human dermal sinus arises after nondisjunction of neural tube and surface ectoderm.
    PMID: 19119900 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2122654</comments>
            <pubDate>Thu, 01 Jan 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2122654</guid>        </item>
        <item>
            <title>Changes in cerebral perfusion hormone profile and cerebrospinal fluid flow across the third ventriculostomy after endoscopic third ventriculostomy in patients with aqueductal stenosis: a prospective study. Clinical article.</title>
            <link>http://www.medworm.com/index.php?rid=2122653&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19119901%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: Clinical improvement is not well correlated with a decrease in ventricular size following ETV. Brain SPECT is a valuable tool for the follow-up of patients with hydrocephalus after ETV, particularly in cases in which MR imaging findings are not clear. There are subtle hormonal changes in patients with hydrocephalus that may improve following ETV.
    PMID: 19119901 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2122653</comments>
            <pubDate>Thu, 01 Jan 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2122653</guid>        </item>
        <item>
            <title>Tentorial cavernous angioma with profuse bleeding. Case report.</title>
            <link>http://www.medworm.com/index.php?rid=2122652&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19119902%26dopt%3DAbstract</link>
            <description>Authors: Mori H, Koike T, Endo S, Takii Y, Uzuka T, Takahashi H, Ito J, Tanaka R
    This 15-year-old boy with a tentorial cavernous angioma reported occasional headache and scintillation in his left visual field. Magnetic resonance imaging revealed a well-demarcated, homogeneously enhanced tumor originating from the right cerebellar tentorium and extending into both the supratentorial and infratentorial spaces. Although a meningioma was suspected, vertebral artery angiography revealed a thickened meningeal branch originating from the right posterior inferior cerebellar artery and flecked tumor stain with pooling of contrast medium until the late venous phase. A cavernous angioma of the tentorium was suspected based on this finding, and as expected from the radiological findings, profuse b...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2122652</comments>
            <pubDate>Thu, 01 Jan 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2122652</guid>        </item>
        <item>
            <title>Congenital cavernous hemangioma of the calvaria. Case report.</title>
            <link>http://www.medworm.com/index.php?rid=2122651&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19119903%26dopt%3DAbstract</link>
            <description>Authors: Vural M, Acikalin MF, Adapinar B, Atasoy MA
    The authors present the case of a 6-month-old infant with a cavernous hemangioma of the parietal bone and discuss the radiological, operative, and pathological features and differential diagnosis of these extremely rare lesions in infants. Only 1 case of an infant with a calvarial cavernous hemangioma without intracranial invasion has previously been reported, and that case involved a 4 month old. Although a cavernous hemangioma of the calvaria is extremely rare in the newborn, this condition should be included in the differential diagnosis of calvarial lesions. During surgical treatment of calvarial cavernous hemangiomas, utmost attention should be paid to avoid blood loss, which could be fatal in infants.
    PMID: 19119903 [PubMed...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2122651</comments>
            <pubDate>Thu, 01 Jan 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2122651</guid>        </item>
        <item>
            <title>Aggressive variant of a papillary glioneuronal tumor. Report of 2 cases.</title>
            <link>http://www.medworm.com/index.php?rid=2122650&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19119904%26dopt%3DAbstract</link>
            <description>Authors: Javahery RJ, Davidson L, Fangusaro J, Finlay JL, Gonzalez-Gomez I, McComb JG
    Papillary glioneuronal tumors are a newly recognized type of brain neoplasm characterized by prominent pseudopapillary structures and glioneuronal elements. All prior cases have shown that these tumors have an indolent course. The authors present 2 patients with an aggressive variant of the tumor. The first patient had dissemination of her tumor and the second had local spreading. Therefore, the authors conclude that papillary glioneuronal tumors do not always behave in a strictly benign fashion.
    PMID: 19119904 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2122650</comments>
            <pubDate>Thu, 01 Jan 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2122650</guid>        </item>
        <item>
            <title>Arteriovenous shunting as a new feature of PHACES. Case report.</title>
            <link>http://www.medworm.com/index.php?rid=2122649&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19119905%26dopt%3DAbstract</link>
            <description>Authors: Wang H, Oh AK, Orbach DB
    Patients with the congenital neurocutaneous disorder PHACES are at a markedly increased risk of ischemic infarction during childhood. Although intracranial arterial anomalies have been well described, venous abnormalities have not been documented. The authors report on a unique case of a 3-month-old girl with PHACES and a skull base osteodural arteriovenous fistula. A separate arteriovenous shunt at T-5 may also have been present. Imaging findings and treatment strategies are discussed.
    PMID: 19119905 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2122649</comments>
            <pubDate>Thu, 01 Jan 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2122649</guid>        </item>
        <item>
            <title>Pediatric spinal clear cell meningioma. Case report.</title>
            <link>http://www.medworm.com/index.php?rid=2122648&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19119906%26dopt%3DAbstract</link>
            <description>In this report the authors describe a unique case of spinal clear cell meningioma in a 13-year-old girl. Clear cell meningiomas (CCMs) are not uncommon. To the authors' knowledge, 14 cases of pediatric CCM occurring in the spinal canal have been reported. Factors lending resistance to meningioma initiation and invasion are analyzed. This 13-year-old girl presented with pain radiating down her left leg. Admission MR imaging showed an inhomogeneous enhancing intradural-extramedullary mass at the L4-5 level. Resection revealed a CCM, and radiotherapy was subsequently administered. Postoperatively there has been no recurrence in &amp;gt; 2 years. In this paper the authors report a case of CCM and provide a comprehensive literature review on this disease. Current recommendations for its management ...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2122648</comments>
            <pubDate>Thu, 01 Jan 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2122648</guid>        </item>
        <item>
            <title>Low-level copy gain versus amplification of myc oncogenes in medulloblastoma: utility in predicting prognosis and survival. Laboratory investigation.</title>
            <link>http://www.medworm.com/index.php?rid=2122647&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19119907%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: Since FISH could easily detect most cases in the moderate-to-high myc gene amplification (&amp;gt; 5-fold CN) group, the FISH assay has utility in detecting subsets of MB with poorer prognosis.
    PMID: 19119907 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2122647</comments>
            <pubDate>Thu, 01 Jan 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2122647</guid>        </item>
        <item>
            <title>Decompressive craniectomy in children with nontraumatic refractory high intracranial pressure. Clinical article.</title>
            <link>http://www.medworm.com/index.php?rid=2122646&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19119908%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: The authors found decompressive craniectomy to be an effective and lifesaving technique in children. This procedure should be included in the arsenal of treatments for nontraumatic intracranial hypertension.
    PMID: 19119908 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2122646</comments>
            <pubDate>Thu, 01 Jan 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2122646</guid>        </item>
        <item>
            <title>Active spontaneous decompression of a suprasellar-prepontine arachnoid cyst detected with routine magnetic resonance imaging. Case report.</title>
            <link>http://www.medworm.com/index.php?rid=2122645&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19119909%26dopt%3DAbstract</link>
            <description>Authors: Thomas BP, Pearson MM, Wushensky CA
    Arachnoid cysts are congenital CSF collections that arise adjacent to arachnoid cisterns. These lesions can be incidental neuroimaging findings but may also cause symptoms and necessitate treatment, particularly in children. The authors present their experience with a male infant harboring a large suprasellar-prepontine arachnoid cyst who underwent spontaneous decompression into the ventricular system, as evidenced by a visualized CSF flow jet observed on routine MR imaging.
    PMID: 19119909 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2122645</comments>
            <pubDate>Thu, 01 Jan 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2122645</guid>        </item>
        <item>
            <title>Management of vagal nerve stimulator infections: do they need to be removed. Clinical article?</title>
            <link>http://www.medworm.com/index.php?rid=2122644&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19119910%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: This study confirms the low rate of infection associated with VNS placement and suggests that, in the case of infection, treatment without removal is a viable option. However, the authors' data suggest that oral antibiotics are not the best first-line therapy.
    PMID: 19119910 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2122644</comments>
            <pubDate>Thu, 01 Jan 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2122644</guid>        </item>
        <item>
            <title>The pediatric neurosurgical workforce: defining the current supply.</title>
            <link>http://www.medworm.com/index.php?rid=2084738&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19119896%26dopt%3DAbstract</link>
            <description>Conclusions The authors estimate that there are fewer than 200 pediatric neurosurgeons currently practicing in the United States. Current practice patterns unique to pediatrics may have important implications in recruiting and retaining the next generation of pediatric neurosurgeons.
    PMID: 19119896 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2084738</comments>
            <pubDate>Thu, 01 Jan 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2084738</guid>        </item>
        <item>
            <title>Intraventricular baclofen for dystonia: techniques and outcomes.</title>
            <link>http://www.medworm.com/index.php?rid=2084737&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19119897%26dopt%3DAbstract</link>
            <description>Conclusions Intraventricular baclofen is an effective method of infusing baclofen to treat severe, generalized secondary dystonia, and, at times, heredodegenerative dystonia. The site of baclofen's activity when treating dystonia may be at the cortical level, and intraventricular infusion may result in higher baclofen concentrations over the cortex than intrathecal infusion. Additional studies are necessary to determine whether IVB is effective at lower doses than those used with intrathecal baclofen administration.
    PMID: 19119897 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2084737</comments>
            <pubDate>Thu, 01 Jan 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2084737</guid>        </item>
        <item>
            <title>Jefferson fractures of the immature spine.</title>
            <link>http://www.medworm.com/index.php?rid=2084736&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19119898%26dopt%3DAbstract</link>
            <description>Authors: Auyong N, Piatt J
    Jefferson fractures of the immature spine have received little attention in the study of pediatric spinal trauma. Fractures through synchondroses are a possibility in the immature spine, in addition to fractures through osseous portions of the vertebral ring, and they create opportunities for misinterpretation of diagnostic imaging. The authors describe 3 examples of Jefferson fractures in young children. All 3 cases featured fractures through an anterior synchondrosis in association with persistence of the posterior synchondrosis or a fracture of the posterior arch. The possibility of a Jefferson fracture should be considered for any child presenting with neck pain, cervical muscle spasm, or torticollis following a head injury, despite a seemingly normal cer...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2084736</comments>
            <pubDate>Thu, 01 Jan 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2084736</guid>        </item>
        <item>
            <title>Computed tomography morphometric analysis for C-1 lateral mass screw placement in children.</title>
            <link>http://www.medworm.com/index.php?rid=2084735&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19119899%26dopt%3DAbstract</link>
            <description>Conclusions A significant variation in the morphological features of C-1 exists, especially between the left and right sides and in younger children. The differences between boys and girls are clinically insignificant. The critical measurement of whether the C-1 lateral mass in a child could accommodate a 3.5-mm-diameter screw is the width of the lateral mass and its proximity to the vertebral artery. Only 1 of 152 lateral masses studied would not have been able to accommodate a lateral mass screw. This study reemphasizes the importance of a preoperative CT scan of the upper cervical spine to assure safe and effective placement of the instrumentation at this level.
    PMID: 19119899 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2084735</comments>
            <pubDate>Thu, 01 Jan 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2084735</guid>        </item>
        <item>
            <title>Spinal congenital dermal sinus in a chick embryo model.</title>
            <link>http://www.medworm.com/index.php?rid=2084734&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19119900%26dopt%3DAbstract</link>
            <description>Conclusions Implantation of donor amniotic tissue in the closing chick neural tube does result in a dimple, from which a strand of tissue continues to the neural tube in various cases, indicating that formation of a dermal sinus-like anomaly can be successfully induced by experimental continuation of the connection between neural tube and surface ectoderm. This finding strengthens the hypothesis that a human dermal sinus arises after nondisjunction of neural tube and surface ectoderm.
    PMID: 19119900 [PubMed - as supplied by publisher] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2084734</comments>
            <pubDate>Thu, 01 Jan 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2084734</guid>        </item>
        <item>
            <title>Changes in cerebral perfusion hormone profile and cerebrospinal fluid flow across the third ventriculostomy after endoscopic third ventriculostomy in patients with aqueductal stenosis: a prospective study.</title>
            <link>http://www.medworm.com/index.php?rid=2084733&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19119901%26dopt%3DAbstract</link>
            <description>Conclusions Clinical improvement is not well correlated with a decrease in ventricular size following ETV. Brain SPECT is a valuable tool for the follow-up of patients with hydrocephalus after ETV, particularly in cases in which MR imaging findings are not clear. There are subtle hormonal changes in patients with hydrocephalus that may improve following ETV.
    PMID: 19119901 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2084733</comments>
            <pubDate>Thu, 01 Jan 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2084733</guid>        </item>
        <item>
            <title>Tentorial cavernous angioma with profuse bleeding.</title>
            <link>http://www.medworm.com/index.php?rid=2084732&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19119902%26dopt%3DAbstract</link>
            <description>Authors: Mori H, Koike T, Endo S, Takii Y, Uzuka T, Takahashi H, Ito J, Tanaka R
    This 15-year-old boy with a tentorial cavernous angioma reported occasional headache and scintillation in his left visual field. Magnetic resonance imaging revealed a well-demarcated, homogeneously enhanced tumor originating from the right cerebellar tentorium and extending into both the supratentorial and infratentorial spaces. Although a meningioma was suspected, vertebral artery angiography revealed a thickened meningeal branch originating from the right posterior inferior cerebellar artery and flecked tumor stain with pooling of contrast medium until the late venous phase. A cavernous angioma of the tentorium was suspected based on this finding, and as expected from the radiological findings, profuse b...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2084732</comments>
            <pubDate>Thu, 01 Jan 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2084732</guid>        </item>
        <item>
            <title>Congenital cavernous hemangioma of the calvaria.</title>
            <link>http://www.medworm.com/index.php?rid=2084731&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19119903%26dopt%3DAbstract</link>
            <description>Authors: Vural M, Acikalin MF, Adapinar B, Atasoy MA
    The authors present the case of a 6-month-old infant with a cavernous hemangioma of the parietal bone and discuss the radiological, operative, and pathological features and differential diagnosis of these extremely rare lesions in infants. Only 1 case of an infant with a calvarial cavernous hemangioma without intracranial invasion has previously been reported, and that case involved a 4 month old. Although a cavernous hemangioma of the calvaria is extremely rare in the newborn, this condition should be included in the differential diagnosis of calvarial lesions. During surgical treatment of calvarial cavernous hemangiomas, utmost attention should be paid to avoid blood loss, which could be fatal in infants.
    PMID: 19119903 [PubMed...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2084731</comments>
            <pubDate>Thu, 01 Jan 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2084731</guid>        </item>
        <item>
            <title>Aggressive variant of a papillary glioneuronal tumor.</title>
            <link>http://www.medworm.com/index.php?rid=2084730&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19119904%26dopt%3DAbstract</link>
            <description>Authors: Javahery RJ, Davidson L, Fangusaro J, Finlay JL, Gonzalez-Gomez I, McComb JG
    Papillary glioneuronal tumors are a newly recognized type of brain neoplasm characterized by prominent pseudopapillary structures and glioneuronal elements. All prior cases have shown that these tumors have an indolent course. The authors present 2 patients with an aggressive variant of the tumor. The first patient had dissemination of her tumor and the second had local spreading. Therefore, the authors conclude that papillary glioneuronal tumors do not always behave in a strictly benign fashion.
    PMID: 19119904 [PubMed - as supplied by publisher] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2084730</comments>
            <pubDate>Thu, 01 Jan 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2084730</guid>        </item>
        <item>
            <title>Arteriovenous shunting as a new feature of PHACES.</title>
            <link>http://www.medworm.com/index.php?rid=2084729&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19119905%26dopt%3DAbstract</link>
            <description>Authors: Wang H, Oh AK, Orbach DB
    Patients with the congenital neurocutaneous disorder PHACES are at a markedly increased risk of ischemic infarction during childhood. Although intracranial arterial anomalies have been well described, venous abnormalities have not been documented. The authors report on a unique case of a 3-month-old girl with PHACES and a skull base osteodural arteriovenous fistula. A separate arteriovenous shunt at T-5 may also have been present. Imaging findings and treatment strategies are discussed.
    PMID: 19119905 [PubMed - as supplied by publisher] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2084729</comments>
            <pubDate>Thu, 01 Jan 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2084729</guid>        </item>
        <item>
            <title>Pediatric spinal clear cell meningioma.</title>
            <link>http://www.medworm.com/index.php?rid=2084728&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19119906%26dopt%3DAbstract</link>
            <description>In this report the authors describe a unique case of spinal clear cell meningioma in a 13-year-old girl. Clear cell meningiomas (CCMs) are not uncommon. To the authors' knowledge, 14 cases of pediatric CCM occurring in the spinal canal have been reported. Factors lending resistance to meningioma initiation and invasion are analyzed. This 13-year-old girl presented with pain radiating down her left leg. Admission MR imaging showed an inhomogeneous enhancing intradural-extramedullary mass at the L4-5 level. Resection revealed a CCM, and radiotherapy was subsequently administered. Postoperatively there has been no recurrence in &amp;gt; 2 years. In this paper the authors report a case of CCM and provide a comprehensive literature review on this disease. Current recommendations for its management ...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2084728</comments>
            <pubDate>Thu, 01 Jan 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2084728</guid>        </item>
        <item>
            <title>Low-level copy gain versus amplification of myc oncogenes in medulloblastoma: utility in predicting prognosis and survival.</title>
            <link>http://www.medworm.com/index.php?rid=2084727&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19119907%26dopt%3DAbstract</link>
            <description>Conclusions Since FISH could easily detect most cases in the moderate-to-high myc gene amplification (&amp;gt; 5-fold CN) group, the FISH assay has utility in detecting subsets of MB with poorer prognosis.
    PMID: 19119907 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2084727</comments>
            <pubDate>Thu, 01 Jan 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2084727</guid>        </item>
        <item>
            <title>Decompressive craniectomy in children with nontraumatic refractory high intracranial pressure.</title>
            <link>http://www.medworm.com/index.php?rid=2084726&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19119908%26dopt%3DAbstract</link>
            <description>Conclusions The authors found decompressive craniectomy to be an effective and lifesaving technique in children. This procedure should be included in the arsenal of treatments for nontraumatic intracranial hypertension.
    PMID: 19119908 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2084726</comments>
            <pubDate>Thu, 01 Jan 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2084726</guid>        </item>
        <item>
            <title>Active spontaneous decompression of a suprasellar-prepontine arachnoid cyst detected with routine magnetic resonance imaging.</title>
            <link>http://www.medworm.com/index.php?rid=2084725&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19119909%26dopt%3DAbstract</link>
            <description>Authors: Thomas BP, Pearson MM, Wushensky CA
    Arachnoid cysts are congenital CSF collections that arise adjacent to arachnoid cisterns. These lesions can be incidental neuroimaging findings but may also cause symptoms and necessitate treatment, particularly in children. The authors present their experience with a male infant harboring a large suprasellar-prepontine arachnoid cyst who underwent spontaneous decompression into the ventricular system, as evidenced by a visualized CSF flow jet observed on routine MR imaging.
    PMID: 19119909 [PubMed - as supplied by publisher] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2084725</comments>
            <pubDate>Thu, 01 Jan 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2084725</guid>        </item>
        <item>
            <title>Management of vagal nerve stimulator infections: do they need to be removed?</title>
            <link>http://www.medworm.com/index.php?rid=2084724&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19119910%26dopt%3DAbstract</link>
            <description>Conclusions This study confirms the low rate of infection associated with VNS placement and suggests that, in the case of infection, treatment without removal is a viable option. However, the authors' data suggest that oral antibiotics are not the best first-line therapy.
    PMID: 19119910 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2084724</comments>
            <pubDate>Thu, 01 Jan 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2084724</guid>        </item>
        <item>
            <title>Ossified pseudomeningocele.</title>
            <link>http://www.medworm.com/index.php?rid=2084723&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19119911%26dopt%3DAbstract</link>
            <description>Authors: Goel A
    
    PMID: 19119911 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2084723</comments>
            <pubDate>Thu, 01 Jan 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2084723</guid>        </item>
        <item>
            <title>Pneumothorax complicating &quot;in-out-in&quot; thoracic pedicle screw placement for kyphotic deformity correction in a child.</title>
            <link>http://www.medworm.com/index.php?rid=1997295&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19035680%26dopt%3DAbstract</link>
            <description>Authors: Viswanathan A, Relyea K, Whitehead WE, Curry DJ, Luerssen TG, Jea A
    The authors describe a rare case of pneumothorax as a complication of thoracic pedicle screw placement in an 11-year-old girl undergoing posterior segmental instrumentation for a kyphotic deformity. Spontaneous pneumothorax after posterior fusion for adolescent idiopathic scoliosis has been reported in the orthopedic literature; however, to the best of the authors' knowledge, pneumothorax directly related to pedicle screw placement for spinal deformity has not been previously described. The authors discuss the anatomical and technical aspects leading to this complication and the lessons learned from it.
    PMID: 19035680 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1997295</comments>
            <pubDate>Sat, 29 Nov 2008 14:31:08 +0100</pubDate>
            <guid isPermaLink="false">1997295</guid>        </item>
        <item>
            <title>Routine imaging in patients with ventriculopleural shunts: lessons learned from a case of tension hydrothorax.</title>
            <link>http://www.medworm.com/index.php?rid=1997294&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19035681%26dopt%3DAbstract</link>
            <description>Authors: Fox BD, Nayar VV, Johnson KK, Jea A, Curry D, Luerssen TG, Whitehead WE
    
    PMID: 19035681 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1997294</comments>
            <pubDate>Sat, 29 Nov 2008 14:31:05 +0100</pubDate>
            <guid isPermaLink="false">1997294</guid>        </item>
        <item>
            <title>Translaminar screw fixation in the subaxial pediatric cervical spine.</title>
            <link>http://www.medworm.com/index.php?rid=1997293&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19035682%26dopt%3DAbstract</link>
            <description>Authors: Jea A, Johnson KK, Whitehead WE, Luerssen TG
    The use of spinal instrumentation to stabilize the occipitocervical junction in pediatric patients has increased and evolved in recent years. Wiring techniques have now given way to screw-rod or screw-plate techniques with or without postoperative external immobilization. Although C-2 translaminar screws have been used in these constructs, subaxial translaminar screws have not, to date, been described in either the pediatric or adult patient populations. The authors describe the feasibility of translaminar screw placement in the C-3 lamina. Rigid fixation with translaminar screws offers an alternative to subaxial fixation with lateral mass screws, allowing for formation of biomechanically sound spinal constructs and minimizing poten...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1997293</comments>
            <pubDate>Sat, 29 Nov 2008 14:30:56 +0100</pubDate>
            <guid isPermaLink="false">1997293</guid>        </item>
        <item>
            <title>Meningioma with dural venous sinus invasion and jugular vein extension.</title>
            <link>http://www.medworm.com/index.php?rid=1997292&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19035683%26dopt%3DAbstract</link>
            <description>Authors: Vachhrajani S, Jea A, Rutka JA, Blaser S, Cusimano M, Rutka JT
    Meningiomas represent the most common benign intracranial neoplasm in adults, with a considerably lower incidence in children. The authors present the case of an intracranial meningioma with invasion of, and intraluminal extension into, the transverse and sigmoid sinuses, jugular bulb, and internal jugular vein, resulting in venous occlusion in a 14-year-old girl. Computed tomography scanning, MR imaging, and conventional angiography were performed preoperatively. The patient underwent a 2-stage resection: the supratentorial component was resected first, and the infratentorial and venous sinus and jugular vein components were subsequently removed using a combined skull base approach. Gross-total resection was achie...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1997292</comments>
            <pubDate>Sat, 29 Nov 2008 14:30:52 +0100</pubDate>
            <guid isPermaLink="false">1997292</guid>        </item>
        <item>
            <title>Pathological satiety caused by brainstem hemangioblastoma.</title>
            <link>http://www.medworm.com/index.php?rid=1997291&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19035684%26dopt%3DAbstract</link>
            <description>Authors: Song DK, Lonser RR
    Because of the multiplicity and saltatory growth pattern associated with central nervous system hemangioblastomas in von Hippel-Lindau (VHL) disease, resection of individual tumors is usually reserved until symptoms occur, to avoid unnecessary surgery over the lifetime of a patient. Brainstem hemangioblastomas in VHL typically cause lower cranial nerve dysfunction, long-tract signs, sensory impairment, and gait abnormalities. The authors report on a 16-year-old girl with VHL who presented with abnormal early satiety resulting in growth and developmental arrest associated with a growing obex hemangioblastoma. Tumor resection resulted in restoration of appetite, with rapid weight gain, growth in stature, and onset of menses. These findings indicate that caudal...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1997291</comments>
            <pubDate>Sat, 29 Nov 2008 14:30:48 +0100</pubDate>
            <guid isPermaLink="false">1997291</guid>        </item>
        <item>
            <title>High-grade primary diffuse leptomeningeal gliomatosis in a child with neurofibromatosis Type 1.</title>
            <link>http://www.medworm.com/index.php?rid=1997290&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19035685%26dopt%3DAbstract</link>
            <description>Authors: King JA, Halliday W, Drake JM
    The authors report on a child with known neurofibromatosis Type 1 who developed high-grade diffuse leptomeningeal gliomatosis, without a known primary glioma. To the authors' knowledge, this is the first report of the coexistence of these conditions in a child.
    PMID: 19035685 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1997290</comments>
            <pubDate>Sat, 29 Nov 2008 14:30:44 +0100</pubDate>
            <guid isPermaLink="false">1997290</guid>        </item>
        <item>
            <title>Intradural inclusion cysts following in utero closure of myelomeningocele: clinical implications and follow-up findings.</title>
            <link>http://www.medworm.com/index.php?rid=1997289&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19035686%26dopt%3DAbstract</link>
            <description>Conclusions Cutaneously derived intradural ICs can develop following fMMC surgery. Deterioration of bladder function, risk of recurrence, and loss of lower-extremity function appear to be the most important long-term complications of IC in children with fMMCs. The ongoing NIH-sponsored MOMS may help determine whether children with fMMC are at increased risk of IC development compared with children treated with postnatal MMC closure. Parents seeking fMMC closure should be informed about the possibility of IC formation and the potential clinical consequences.
    PMID: 19035686 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1997289</comments>
            <pubDate>Sat, 29 Nov 2008 14:30:23 +0100</pubDate>
            <guid isPermaLink="false">1997289</guid>        </item>
        <item>
            <title>Congenital dermoid tumor in a child at initial myelomeningocele closure: an etiological discussion.</title>
            <link>http://www.medworm.com/index.php?rid=1997288&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19035687%26dopt%3DAbstract</link>
            <description>Authors: Ramos E, Marlin AE, Gaskill SJ
    The authors report on a case of a full-term infant with lumbar myelomeningocele who was found to have an intramedullary mass at the time of surgical repair of the defect. The intramedullary mass was consistent with a dermoid tumor both macroscopically and microscopically. This case provides evidence that dermoid tumors occurring at the site of previous surgical myelomeningocele repair are not always a consequence of incomplete excision of the dermal elements.
    PMID: 19035687 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1997288</comments>
            <pubDate>Sat, 29 Nov 2008 14:30:18 +0100</pubDate>
            <guid isPermaLink="false">1997288</guid>        </item>
        <item>
            <title>Atraumatic epidural hematoma secondary to a venous sinus thrombosis: a novel finding.</title>
            <link>http://www.medworm.com/index.php?rid=1997287&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19035688%26dopt%3DAbstract</link>
            <description>Authors: Knopman J, Tsiouris AJ, Souweidane MM
    Venous sinus thrombosis is a rare entity that usually arises secondary to underlying thrombophilia, neoplasm, head injury, or infection. Tympanic infection accounts for the majority of infectious etiologies, and the sigmoid sinus becomes the likely anatomical site of thrombosis. The authors report a case involving a child with recurrent otitis media who presented with an atraumatic epidural hematoma secondary to sigmoid sinus thrombosis. Intraoperative evaluation revealed epidural hemorrhage that originated from the venous sinus, with hemorrhagic products of varying ages. To the authors' knowledge, this is the first reported case of a venous sinus thrombosis resulting in an epidural hematoma.
    PMID: 19035688 [PubMed - in process] (Sourc...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1997287</comments>
            <pubDate>Sat, 29 Nov 2008 14:30:14 +0100</pubDate>
            <guid isPermaLink="false">1997287</guid>        </item>
        <item>
            <title>Supraorbital approach for repair of open anterior skull base fracture.</title>
            <link>http://www.medworm.com/index.php?rid=1997286&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19035689%26dopt%3DAbstract</link>
            <description>Authors: Szabo KA, Cheshier SH, Kalani MY, Kim JW, Guzman R
    To the authors' knowledge, this is the first report of the use of anterior orbitotomy via the supraorbital eyelid crease to repair a dural tear caused by an orbital roof fracture. When transorbital penetrating injuries occur in children, they are commonly caused by accidental falls onto pointed objects. The authors report on their experience with a 7-year-old girl who fell onto a blunt metal rod hanger that penetrated her left eyelid, traversed superior to the eye globe, and penetrated the orbital roof at a depth of 3-4 cm, lacerating the dura mater and entering the cerebrum. An anterior transpalpebral transorbital approach was used to perform the microsurgical anterior skull base and dural repair. The authors advocate the app...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1997286</comments>
            <pubDate>Sat, 29 Nov 2008 14:30:04 +0100</pubDate>
            <guid isPermaLink="false">1997286</guid>        </item>
        <item>
            <title>Radiolucent hair accessories causing depressed skull fracture following blunt cranial trauma.</title>
            <link>http://www.medworm.com/index.php?rid=1997285&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19035690%26dopt%3DAbstract</link>
            <description>Authors: Syed ON, Hankinson TC, Mack WJ, Feldstein NA, Anderson RC
    Pediatric neurosurgeons frequently care for children with traumatic scalp and skull injury. Foreign objects are often observed on imaging and may influence the clinician's decision-making process. The authors report on 2 cases of poorly visualized hair beads that had become embedded into the skull during blunt trauma. In both cases, skull radiography and CT scanning demonstrated depressed, comminuted fractures with poorly demonstrated spherical radiolucencies in the overlying scalp. The nature of these objects was initially unclear, and they could have represented air that entered the scalp during trauma. In one case, scalp inspection demonstrated no evidence of the bead. In the other case, a second bead was observed at...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1997285</comments>
            <pubDate>Sat, 29 Nov 2008 14:29:56 +0100</pubDate>
            <guid isPermaLink="false">1997285</guid>        </item>
        <item>
            <title>Role of external ventriculostomy in the management of fever after hemispherectomy.</title>
            <link>http://www.medworm.com/index.php?rid=1997284&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19035691%26dopt%3DAbstract</link>
            <description>Conclusions The use of external ventriculostomy following hemispherectomy for intractable epilepsy in children reduces the incidence of postoperative fever due to infection.
    PMID: 19035691 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1997284</comments>
            <pubDate>Sat, 29 Nov 2008 14:29:45 +0100</pubDate>
            <guid isPermaLink="false">1997284</guid>        </item>
        <item>
            <title>The use of noninvasive electromagnetic neuronavigation for slit ventricle syndrome and complex hydrocephalus in a pediatric population.</title>
            <link>http://www.medworm.com/index.php?rid=1997283&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19035692%26dopt%3DAbstract</link>
            <description>Conclusions Electromagnetic neuronavigation using a frameless and pinless system is especially suited for pediatric patients. The authors hypothesize that successful placement of ventricular catheters will reduce morbidity and improve shunt longevity.
    PMID: 19035692 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1997283</comments>
            <pubDate>Sat, 29 Nov 2008 14:29:30 +0100</pubDate>
            <guid isPermaLink="false">1997283</guid>        </item>
        <item>
            <title>Rhombencephalosynapsis associated with autosomal dominant polycystic kidney disease Type 1.</title>
            <link>http://www.medworm.com/index.php?rid=1997282&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19035693%26dopt%3DAbstract</link>
            <description>Authors: Elliott R, Harter DH
    Rhombencephalosynapsis (RES) is a rare congenital malformation of the cerebellum characterized by hypogenesis or agenesis of the vermis and fusion of the cerebellar hemispheres with or without fusion of the dentate nuclei and superior cerebellar peduncles. No genetic or chromosomal abnormalities have been identified for RES. Although the occurrence of RES is presumed to be sporadic, no clear pattern of inheritance has been identified. The authors report on a 17-year-old girl with autosomal dominant polycystic kidney disease Type 1 as well as RES.
    PMID: 19035693 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1997282</comments>
            <pubDate>Sat, 29 Nov 2008 14:29:26 +0100</pubDate>
            <guid isPermaLink="false">1997282</guid>        </item>
        <item>
            <title>Quick-brain magnetic resonance imaging for nonhydrocephalus indications.</title>
            <link>http://www.medworm.com/index.php?rid=1997281&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19035694%26dopt%3DAbstract</link>
            <description>Conclusions The role of QB MR imaging for nonhydrocephalic indications is expanding, and it appears promising for a number of screening and surveillance paradigms. &quot;Quick-brain plus&quot; protocols for specific indications may add sensitivity and are under development.
    PMID: 19035694 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1997281</comments>
            <pubDate>Sat, 29 Nov 2008 14:29:18 +0100</pubDate>
            <guid isPermaLink="false">1997281</guid>        </item>
        <item>
            <title>Can intraoperative assessment of endoscopic third ventriculostomy predict success?</title>
            <link>http://www.medworm.com/index.php?rid=1931067&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18976096%26dopt%3DAbstract</link>
            <description>Authors: Drake JM, Riva-Cambrin J
    
    PMID: 18976096 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1931067</comments>
            <pubDate>Sat, 01 Nov 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1931067</guid>        </item>
        <item>
            <title>Intraoperative assessment of endoscopic third ventriculostomy success.</title>
            <link>http://www.medworm.com/index.php?rid=1931066&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18976097%26dopt%3DAbstract</link>
            <description>Conclusions Despite reliance in recent years on post-ETV MR images and externalized ventricular monitoring, these modalities, although often useful adjuncts, appear less reliable as predictive tests than a simple assessment at the time of endoscopic fenestration. By using a uniform grading scale, the authors have introduced a novel means through which intraoperative and postoperative decision making can be aided, with the goal of reducing unnecessary procedures and tests and preventing unnecessary returns to the operating room.
    PMID: 18976097 [PubMed - as supplied by publisher] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1931066</comments>
            <pubDate>Sat, 01 Nov 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1931066</guid>        </item>
        <item>
            <title>Failure to treat obstructive hydrocephalus with endoscopic third ventriculostomy in a patient with neurodegenerative Langerhans cell histiocytosis.</title>
            <link>http://www.medworm.com/index.php?rid=1931065&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18976098%26dopt%3DAbstract</link>
            <description>Authors: Kershenovich A, Price AV, Koral K, Goldman S, Swift DM
    The second most frequent central nervous system involvement pattern in Langerhans cell histiocytosis (LCH) is a rare condition documented in a number of reports called &quot;neurodegenerative LCH&quot; (ND-LCH). Magnetic resonance images confirming the presence of the disease usually demonstrate striking symmetric bilateral hyperintensities predominantly in the cerebellum, basal ganglia, pons, and/or cerebral white matter. The authors here describe for the first time in the literature a patient with ND-LCH and concomitant hydrocephalus initially treated using endoscopic third ventriculostomy (ETV). This 9-year-old boy, who had undergone chemotherapy for skin and lung LCH without central nervous system involvement at the age of 10 mo...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1931065</comments>
            <pubDate>Sat, 01 Nov 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1931065</guid>        </item>
        <item>
            <title>Combined endoscopic third ventriculostomy and choroid plexus cauterization as primary treatment of hydrocephalus for infants with myelomeningocele: long-term results of a prospective intent-to-treat study in 115 East African infants.</title>
            <link>http://www.medworm.com/index.php?rid=1931064&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18976099%26dopt%3DAbstract</link>
            <description>Conclusions Using ETV-CPC appears to successfully provide a more durable primary treatment of hydrocephalus for infants with spina bifida than does shunt placement. These results support ETV-CPC as the better treatment option for these children in developing countries.
    PMID: 18976099 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1931064</comments>
            <pubDate>Sat, 01 Nov 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1931064</guid>        </item>
        <item>
            <title>Spontaneous resolution of Chiari malformation Type I in monozygotic twins.</title>
            <link>http://www.medworm.com/index.php?rid=1931063&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18976100%26dopt%3DAbstract</link>
            <description>Authors: Miller JH, Limbrick DD, Callen M, Smyth MD
    The spontaneous resolution of isolated tonsillar ectopia in Chiari malformation Type I (CM-I) is a known and reported entity in 2 previous single study case reports. However, it has not been previously described in monozygotic twins. Two children, ~ 1 year of age with CM-I and presumed episodes of pallid syncope or breath-holding spells presented for neurosurgical evaluation. Although Chiari decompression was considered, the authors decided to proceed with conservative management with close follow-up due to the uncertain nature of these episodes. Approximately 4 years later, both children's symptoms had resolved. Repeated MR imaging examinations also showed spontaneous resolution of the malformation in both girls. These cases emphasiz...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1931063</comments>
            <pubDate>Sat, 01 Nov 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1931063</guid>        </item>
        <item>
            <title>Closer but not there yet: models in child injury research.</title>
            <link>http://www.medworm.com/index.php?rid=1931062&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18976101%26dopt%3DAbstract</link>
            <description>Authors: Duhaime AC, Dodge CP
    
    PMID: 18976101 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1931062</comments>
            <pubDate>Sat, 01 Nov 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1931062</guid>        </item>
        <item>
            <title>Potential for head injuries in infants from low-height falls.</title>
            <link>http://www.medworm.com/index.php?rid=1931061&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18976102%26dopt%3DAbstract</link>
            <description>Conclusions These are the first 3D angular acceleration and impact force data available for head impact in infants from low-height falls. A future study involving a computational model of the infant head will use the loads measured in this study to predict the probability of occipital skull fracture on impact from head-first low-height falls. Together, these studies will provide data that will aid clinicians in the evaluation of accidental and inflicted head injuries, and will contribute to the design of safer environments for children.
    PMID: 18976102 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1931061</comments>
            <pubDate>Sat, 01 Nov 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1931061</guid>        </item>
        <item>
            <title>Intracranial teratomas in children: the role and timing of surgical removal.</title>
            <link>http://www.medworm.com/index.php?rid=1931060&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18976103%26dopt%3DAbstract</link>
            <description>Conclusions The results of this study support the belief that microsurgical removal is the only effective treatment for intracranial teratomas. Surgery may be performed as the primary therapy when there is evidence of a noninvasive teratoma, and as a secondary therapy if there is only a partial response to neoadjuvant therapy or if progression is observed in mixed malignant germ cell tumors.
    PMID: 18976103 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1931060</comments>
            <pubDate>Sat, 01 Nov 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1931060</guid>        </item>
        <item>
            <title>Long-term survival in a child with a central nervous system medulloepithelioma.</title>
            <link>http://www.medworm.com/index.php?rid=1931059&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18976104%26dopt%3DAbstract</link>
            <description>Authors: Moftakhar P, Fan X, Hurvitz CH, Black KL, Danielpour M
    Central nervous system medulloepitheliomas are extremely rare and malignant (World Health Organization Grade IV) primitive neuroectodermal tumors (PNETs) that arise in childhood. Unlike other PNETs, medulloepitheliomas have a dismal prognosis, with only 2 reported cases in the literature in which the patient survived beyond 5 years after treatment. The authors report on the third known case of a child who survived longer than 5 years. A review of all the published cases of medulloepithelioma is also presented, and alternative treatment strategies for PNET tumors, including high-dose chemotherapy with stem-cell rescue, are discussed.
    PMID: 18976104 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1931059</comments>
            <pubDate>Sat, 01 Nov 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1931059</guid>        </item>
        <item>
            <title>Long-term survival of an infant with gliomatosis cerebelli.</title>
            <link>http://www.medworm.com/index.php?rid=1931058&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18976105%26dopt%3DAbstract</link>
            <description>In this report the authors document the surgical treatment of a 13-month-old boy whose tumor arose in the cerebellum and over time extended to the thalamus where its growth halted at age 3 years and 10 months. Aside from 2 partial resections the patient underwent neither radiotherapy nor chemotherapy. He is now 21 years old and functions independently.
    PMID: 18976105 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1931058</comments>
            <pubDate>Sat, 01 Nov 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1931058</guid>        </item>
        <item>
            <title>Neurenteric cyst with xanthomatous changes in the prepontine area: unusual radiological findings.</title>
            <link>http://www.medworm.com/index.php?rid=1931057&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18976106%26dopt%3DAbstract</link>
            <description>Authors: Ko BS, Jung S, Jung TY, Moon KS, Kim IY, Kang SS
    Preoperative diagnosis of neurenteric cysts can be difficult because the imaging findings of a neurenteric cyst may be similar to those of an arachnoid cyst. The authors report a case of a neurenteric cyst with xanthomatous changes in the prepontine area. This 4-year-old girl was admitted to their institution with intermittent neck pain and vomiting. Computed tomography showed a hypodense mass in the prepontine area. Magnetic resonance imaging showed a cystic lesion measuring ~ 4 x 3 cm. The brainstem was displaced posteriorly, and the cisterns in both cerebellopontine angles were widened. The signal intensity of the cyst was similar to that of cerebrospinal fluid. Adjacent to the basilar artery there was a solid component of th...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1931057</comments>
            <pubDate>Sat, 01 Nov 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1931057</guid>        </item>
        <item>
            <title>Herpes simplex encephalitis after craniopharyngioma surgery.</title>
            <link>http://www.medworm.com/index.php?rid=1931056&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18976107%26dopt%3DAbstract</link>
            <description>Authors: Kwon JW, Cho BK, Kim EC, Wang KC, Kim SK
    A 13-year-old girl exhibited rapid deterioration in mental status 15 days after surgery for craniopharyngioma. Serial CT scanning detected progression of a low-density lesion on the left frontotemporal lobe. The serum level of C-reactive protein was elevated and polymerase chain reaction identified herpes simplex virus DNA in the cerebrospinal fluid. Antiviral therapy with high-dose acyclovir (10 mg/kg 3 times daily) was begun. She recovered and could speak short sentences, but dysphasia and right hemiparesis remained. Early diagnosis and active treatment of herpes simplex encephalitis is essential for improving prognosis and saving lives.
    PMID: 18976107 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1931056</comments>
            <pubDate>Sat, 01 Nov 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1931056</guid>        </item>
        <item>
            <title>Failed age-dependent maturation of the occipital condyle in patients with congenital occipitoatlantal instability and Down syndrome: a preliminary analysis.</title>
            <link>http://www.medworm.com/index.php?rid=1931055&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18976108%26dopt%3DAbstract</link>
            <description>Conclusions Patient with DS/COI who have occipitoatlantal instability fail to develop the curved architecture in the occipital condyle that occurs in age-matched controls over time. Sagittal 2D CT reconstructions accurately determine the precise structure of the occipital condyle, although the indications for CT scanning are limited. Because of the poor intra- and interrater reliability on static plain radiographs, dynamic flexion/extension cervical spine radiographs remain the study of choice by which to directly evaluate occipitocervical motion.
    PMID: 18976108 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1931055</comments>
            <pubDate>Sat, 01 Nov 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1931055</guid>        </item>
        <item>
            <title>Percutaneous intralesional injection of calcitonin and methylprednisolone for treatment of an aneurysmal bone cyst at C-2.</title>
            <link>http://www.medworm.com/index.php?rid=1931054&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18976109%26dopt%3DAbstract</link>
            <description>Authors: Ohashi M, Ito T, Hirano T, Endo N
    An aneurysmal bone cyst (ABC) is a rare skeletal tumor that accounts for ~ 1% of all bone tumors. A spinal location for an ABC is very rare. Methods for treatment of an ABC include resection, curettage, embolization, and intralesional injection of a variety of agents. The patient in this case was a 9-year-old girl presenting with neck pain who was diagnosed with an ABC involving the C-2 spinal level. Percutaneous intralesional injections of calcitonin and methylprednisolone were performed. Two years and 7 months after the initial injection, a CT scan showed massive bone formation and cortical thickening without a change in the size of the lesion. To the authors' knowledge, this is the third reported case of intralesional injection of calcitoni...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1931054</comments>
            <pubDate>Sat, 01 Nov 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1931054</guid>        </item>
        <item>
            <title>Diagnosing cranial fasciitis based on distinguishing radiological features.</title>
            <link>http://www.medworm.com/index.php?rid=1931053&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18976110%26dopt%3DAbstract</link>
            <description>Authors: Johnson KK, Dannenbaum MJ, Bhattacharjee MB, Illner A, Dauser RC, Whitehead WE, Jea A, Luerssen TG
    Primary skull lesions, albeit rare in the pediatric population, have been well described and classified. These lesions are usually benign and commonly present as a painless mass. The most common lesions are epidermoid, dermoid, and Langerhans cell histiocytosis. Cranial fasciitis, encountered less frequently, is usually not considered in this differential diagnosis. Given such few cases reported, it is commonly misdiagnosed preoperatively. The authors retrospectively reviewed data obtained in 4 patients with cranial fasciitis in whom the diagnosis was based on histopathological findings. In 2 patients the onset of the lesion was spontaneous. One patient had a lesion 4 months foll...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1931053</comments>
            <pubDate>Sat, 01 Nov 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1931053</guid>        </item>
        <item>
            <title>Vagus nerve stimulation.</title>
            <link>http://www.medworm.com/index.php?rid=1931052&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18976111%26dopt%3DAbstract</link>
            <description>Authors: Ross IB, Maleeva T, Sutherling WW
    
    PMID: 18976111 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1931052</comments>
            <pubDate>Sat, 01 Nov 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1931052</guid>        </item>
        <item>
            <title>Vagus nerve stimulation.</title>
            <link>http://www.medworm.com/index.php?rid=1931051&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18976112%26dopt%3DAbstract</link>
            <description>Authors: De Ti&amp;#xE8;ge X, Legros B, de Beeck MO, Goldman S, Van Bogaert P
    
    PMID: 18976112 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1931051</comments>
            <pubDate>Sat, 01 Nov 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1931051</guid>        </item>
        <item>
            <title>Transcavum interforniceal endoscopic surgery of the third ventricle.</title>
            <link>http://www.medworm.com/index.php?rid=1851668&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18831654%26dopt%3DAbstract</link>
            <description>Conclusions In the presence of a CSP and CV, endoscopic navigation into the third ventricle can be problematic via a transforaminal approach. Alternatively, a transcavum interforniceal route for endoscopic surgery in the third ventricle is suggested, with the rostral lamina and the anterior commissure as important anatomical landmarks. Endoscopic third ventriculostomy and endoscopic colloid cyst resection performed via a transcavum interforniceal route in patients with a coexistent septal cavum is a feasible and safe option.
    PMID: 18831654 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1851668</comments>
            <pubDate>Wed, 01 Oct 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1851668</guid>        </item>
        <item>
            <title>Pediatric traumatic brain injury and elevated intracranial pressure.</title>
            <link>http://www.medworm.com/index.php?rid=1851667&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18831655%26dopt%3DAbstract</link>
            <description>Authors: Marshall LF
    
    PMID: 18831655 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1851667</comments>
            <pubDate>Wed, 01 Oct 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1851667</guid>        </item>
        <item>
            <title>Long-term outcomes and prognostic factors in pediatric patients with severe traumatic brain injury and elevated intracranial pressure.</title>
            <link>http://www.medworm.com/index.php?rid=1851666&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18831656%26dopt%3DAbstract</link>
            <description>Conclusions Controlling elevated ICP is an important factor in patient survival following severe pediatric TBI. The modality used for ICP control appears to be less important. Long-term follow-up is essential to determine neurocognitive sequelae associated with TBI.
    PMID: 18831656 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1851666</comments>
            <pubDate>Wed, 01 Oct 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1851666</guid>        </item>
        <item>
            <title>Incomplete lateral medullary syndrome in a patient with Chiari malformation Type I presenting with combined trigeminal and vagal nerve dysfunction.</title>
            <link>http://www.medworm.com/index.php?rid=1851665&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18831657%26dopt%3DAbstract</link>
            <description>Authors: Dahdaleh NS, Menezes AH
    The combination of unilateral trigeminal and vagal nerve dysfunction is a rare presentation in patients with Chiari malformation Type I (CM-I). The authors present a case of incomplete lateral medullary syndrome in a patient with CM-I. The patient's symptoms of decreased unilateral facial sensitivity to pain and temperature and her vocal cord dysfunction reversed after posterior fossa decompression and intradural exploration. Although rare, clinicians should be aware of this presentation as part of a protean spectrum of symptoms in patients with CM-I.
    PMID: 18831657 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1851665</comments>
            <pubDate>Wed, 01 Oct 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1851665</guid>        </item>
        <item>
            <title>Clinical predictors of developmental outcome in patients with cephaloceles.</title>
            <link>http://www.medworm.com/index.php?rid=1851664&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18831658%26dopt%3DAbstract</link>
            <description>Conclusions To the authors' knowledge, this is one of the largest North American cephalocele series documented. Unlike prior studies, location of the cephaloceles is not a significant predictor of outcome. The multivariable regression analysis demonstrates hydrocephalus and the presence of associated intracranial abnormalities as variables with cumulative predictive effects for developmental delay.
    PMID: 18831658 [PubMed - as supplied by publisher] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1851664</comments>
            <pubDate>Wed, 01 Oct 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1851664</guid>        </item>
        <item>
            <title>Spina bifida occulta and monozygotic twins.</title>
            <link>http://www.medworm.com/index.php?rid=1851663&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18831659%26dopt%3DAbstract</link>
            <description>We report on a case of different presentations of spina bifida occulta in monozygotic twins. The first twin presented at birth with a lipomyelomeningocele; a tethered cord was diagnosed in the second twin at 2 years of age. Neural tube defects (NTDs) are a group of common congenital malformations of the brain and spine generated during neurulation. The genetic basis of this process is still not well known. Whenever an NTD is diagnosed in one of a pair of twins, the other twin should also be evaluated for NTDs.
    PMID: 18831659 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1851663</comments>
            <pubDate>Wed, 01 Oct 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1851663</guid>        </item>
        <item>
            <title>Expanded endoscopic endonasal resection of an olfactory schwannoma.</title>
            <link>http://www.medworm.com/index.php?rid=1851662&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18831660%26dopt%3DAbstract</link>
            <description>Authors: Kanaan HA, Gardner PA, Yeaney G, Prevedello DM, Monaco EA, Murdoch G, Pollack IF, Kassam AB
    Olfactory schwannomas are rare tumors of the anterior skull base that are possibly derived from ectopic Schwann cells, perivascular neural tissue, or sensory nerves of the meninges. The authors report the case of a 14-year-old boy with an olfactory schwannoma that extended inferiorly through the cranial base and superiorly into the frontal lobe. Because of the growth characteristics of the tumor and the significant overlying frontal lobe edema, the lesion was approached via an endonasal endoscopic route, as a strategy to minimize brain retraction. This tumor was characterized radiographically as contrast-enhancing with cystic areas and erosion into bone. The tumor showed immunoreactivit...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1851662</comments>
            <pubDate>Wed, 01 Oct 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1851662</guid>        </item>
        <item>
            <title>Frontal intradiploic angioleiomyoma.</title>
            <link>http://www.medworm.com/index.php?rid=1851661&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18831661%26dopt%3DAbstract</link>
            <description>Authors: Vijayasaradhi M, Uppin SG, Sreedhar V, Sundaram C, Panigrahi MK
    A left frontal intradiploic angioleiomyoma in a 10-year-old girl is presented with a review of the literature. The pathological and differential diagnosis and management of this rare lesion is discussed.
    PMID: 18831661 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1851661</comments>
            <pubDate>Wed, 01 Oct 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1851661</guid>        </item>
        <item>
            <title>Third ventricular chordoid meningioma in a child.</title>
            <link>http://www.medworm.com/index.php?rid=1851660&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18831662%26dopt%3DAbstract</link>
            <description>Authors: Song KS, Park SH, Cho BK, Wang KC, Phi JH, Kim SK
    Meningiomas are rare in children. Chordoid meningioma is a very rare variant, as only 16 cases in children have been reported. The authors report the first case of a chordoid meningioma in the third ventricle. A 12-year-old boy presented with headache, abnormal behaviors, and ataxia. Brain MR imaging revealed a 2-cm, well-enhanced mass in the third ventricle and hydrocephalus. Positron emission tomography with [(18)F]fluorodeoxyglucose showed that the mass was hypermetabolic. Gross-total removal of the mass was performed using a left frontal transcortical and transventricular approach. The mass originated from the left caudate head and was connected to the choroid plexus. A chordoid meningioma was diagnosed on the basis of the ...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1851660</comments>
            <pubDate>Wed, 01 Oct 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1851660</guid>        </item>
        <item>
            <title>Lymphangioma of the skull base bones leading to cerebrospinal fluid rhinorrhea.</title>
            <link>http://www.medworm.com/index.php?rid=1851659&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18831663%26dopt%3DAbstract</link>
            <description>Authors: Ito E, Saito K, Nagatani T, Teranishi M, Kamei Y, Yagi S, Kawabe T, Niimi N, Yoshida J
    Lymphangioma localized to the bones of the skull base is rare. The authors report herein the case of a 5-year-old boy who presented with lymphangioma of the bone, localized to the skull base and leading to cerebrospinal fluid (CSF) rhinorrhea with meningitis. Neuroimaging demonstrated lytic destruction with a cyst in the right middle skull base. The patient was successfully treated with resection of the tumor and prevention of CSF leakage. Histopathological examination revealed a lymphangioma. An enlarging lymphangioma can lead to bone destruction. A differential diagnosis of a lytic lesion for a cyst at the skull base is important for proper case management.
    PMID: 18831663 [PubMed - as ...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1851659</comments>
            <pubDate>Wed, 01 Oct 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1851659</guid>        </item>
        <item>
            <title>Correlation of a preoperative grading scale with progressive spinal deformity following surgery for intramedullary spinal cord tumors in children.</title>
            <link>http://www.medworm.com/index.php?rid=1851658&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18831664%26dopt%3DAbstract</link>
            <description>Conclusions Application of this grading scheme to a series of resected pediatric IMSCTs has demonstrated its correlation with the incidence of postoperative progressive spinal deformity requiring fusion. The application of a standardized grading scheme will assist in the process of surgical decision making and postoperative evaluation.
    PMID: 18831664 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1851658</comments>
            <pubDate>Wed, 01 Oct 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1851658</guid>        </item>
        <item>
            <title>Laparoscopic placement of distal ventriculoperitoneal shunt catheters.</title>
            <link>http://www.medworm.com/index.php?rid=1851657&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18831665%26dopt%3DAbstract</link>
            <description>Conclusions Laparoscopic placement of distal VPS catheters is relatively safe and allows insertion via inconspicuous incisions. It can allow for inspection or lysis of adhesions and removal of foreign bodies, help determine if and where the abdomen can absorb shunt fluid, and make VPS surgery in the obese patient easier.
    PMID: 18831665 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1851657</comments>
            <pubDate>Wed, 01 Oct 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1851657</guid>        </item>
        <item>
            <title>Thrombosis associated with ventriculoatrial shunts.</title>
            <link>http://www.medworm.com/index.php?rid=1851656&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18831666%26dopt%3DAbstract</link>
            <description>Conclusions Patients with VA shunts represent a unique group at risk for thrombosis. The duration of anticoagulation therapy must be individualized. However, larger studies are needed to evaluate the efficacy of screening for asymptomatic thrombosis and to investigate the role of prophylactic anticoagulation.
    PMID: 18831666 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1851656</comments>
            <pubDate>Wed, 01 Oct 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1851656</guid>        </item>
        <item>
            <title>Ultrasound guidance.</title>
            <link>http://www.medworm.com/index.php?rid=1851655&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18831667%26dopt%3DAbstract</link>
            <description>Authors: Piatt JH
    
    PMID: 18831667 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1851655</comments>
            <pubDate>Wed, 01 Oct 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1851655</guid>        </item>
        <item>
            <title>Shunt infection.</title>
            <link>http://www.medworm.com/index.php?rid=1851654&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18831668%26dopt%3DAbstract</link>
            <description>Authors: Moriyama E, Terada H
    
    PMID: 18831668 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1851654</comments>
            <pubDate>Wed, 01 Oct 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1851654</guid>        </item>
        <item>
            <title>Magnetic resonance angiography in the evaluation of infants with hydrocephalus: a new standard?</title>
            <link>http://www.medworm.com/index.php?rid=1751382&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18759595%26dopt%3DAbstract</link>
            <description>Authors: Dumont AS, Crowley RW, Yeoh HK
    
    PMID: 18759595 [PubMed - as supplied by publisher] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1751382</comments>
            <pubDate>Mon, 01 Sep 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1751382</guid>        </item>
        <item>
            <title>Magnetic resonance imaging for quantitative flow measurement in infants with hydrocephalus: a prospective study.</title>
            <link>http://www.medworm.com/index.php?rid=1751381&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18759596%26dopt%3DAbstract</link>
            <description>Conclusions Magnetic resonance imaging can be used to measure CBF in infants with hydrocephalus. Raised ICP was related to a decrease in CBF. After CSF diversion, CBF and ICP improved to values within the normal range.
    PMID: 18759596 [PubMed - as supplied by publisher] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1751381</comments>
            <pubDate>Mon, 01 Sep 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1751381</guid>        </item>
        <item>
            <title>Treatment of pediatric intracranial vascular malformations using Onyx-18.</title>
            <link>http://www.medworm.com/index.php?rid=1751380&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18759597%26dopt%3DAbstract</link>
            <description>Conclusions Onyx-18 is a feasible embolization agent for use in intracranial vascular malformations in the pediatric population, but long-term follow-up data will be necessary to assess the continued efficacy and safety of this agent.
    PMID: 18759597 [PubMed - as supplied by publisher] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1751380</comments>
            <pubDate>Mon, 01 Sep 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1751380</guid>        </item>
        <item>
            <title>Natural history of the Chiari Type I anomaly.</title>
            <link>http://www.medworm.com/index.php?rid=1751379&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18759598%26dopt%3DAbstract</link>
            <description>Authors: Rekate HL
    
    PMID: 18759598 [PubMed - as supplied by publisher] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1751379</comments>
            <pubDate>Mon, 01 Sep 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1751379</guid>        </item>
        <item>
            <title>The natural history of the Chiari Type I anomaly.</title>
            <link>http://www.medworm.com/index.php?rid=1751378&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18759599%26dopt%3DAbstract</link>
            <description>Conclusions The authors' data confirm the common impression that in both asymptomatic and slightly symptomatic patients with CM-I, a conservative approach to treatment should be adopted with periodic clinical and radiological examinations.
    PMID: 18759599 [PubMed - as supplied by publisher] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1751378</comments>
            <pubDate>Mon, 01 Sep 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1751378</guid>        </item>
        <item>
            <title>Postnatal ascent of the cerebellar tonsils in Chiari malformation Type II following surgical repair of myelomeningocele.</title>
            <link>http://www.medworm.com/index.php?rid=1751377&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18759600%26dopt%3DAbstract</link>
            <description>Conclusions Patients showed ascent of the cerebellar tonsils after postnatal myelomeningocele repair. Placement of a VP shunt helped promote the ascent. However, postnatal myelomeningocele repair in the patients in Group 1 failed to consistently prevent development of symptomatic CM-II. This limited experience suggests that postnatal repair of myelomeningocele can partially reverse the anatomical CM-II, but symptomatic CM-II cannot be prevented in some patients when the repair is performed after 36 weeks' gestation.
    PMID: 18759600 [PubMed - as supplied by publisher] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1751377</comments>
            <pubDate>Mon, 01 Sep 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1751377</guid>        </item>
        <item>
            <title>The Dandy-Walker variant: a case series of 24 pediatric patients and evaluation of associated anomalies, incidence of hydrocephalus, and developmental outcomes.</title>
            <link>http://www.medworm.com/index.php?rid=1751376&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18759601%26dopt%3DAbstract</link>
            <description>Conclusions The DWV was associated with both extra- and intracranial anomalies. Associated radiographic abnormalities including ventriculomegaly were observed. Hydrocephalus requiring cerebrospinal fluid diversion may be indicated. Isolated DWV was associated with a good developmental outcome.
    PMID: 18759601 [PubMed - as supplied by publisher] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1751376</comments>
            <pubDate>Mon, 01 Sep 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1751376</guid>        </item>
        <item>
            <title>Two-year-old girl with cervicomedullary junction stenosis and an unknown type of skeletal dysplasia.</title>
            <link>http://www.medworm.com/index.php?rid=1751375&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18759602%26dopt%3DAbstract</link>
            <description>Authors: Cheshier SH, Kalani MY, Pendakaur A, Higgins D, Kahn D, Shendel S, Shuer L
    The authors present a novel case of skeletal dysplasia in a 2.8-year-old girl. The patient presented with progressive lower cranial nerve palsy and myelopathy due to constriction at the cervicomedullary junction caused by overgrowth of the occipital bone of the foramen magnum and the C-1. She also had prominent bone overgrowth of the superior orbital ridges, resulting in excessive stretching of periorbital skin and an inability to fully close her eyes.
    PMID: 18759602 [PubMed - as supplied by publisher] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1751375</comments>
            <pubDate>Mon, 01 Sep 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1751375</guid>        </item>
        <item>
            <title>Ossified pseudomeningocele following Chiari decompression surgery in a patient with Kleeblattschädel deformity.</title>
            <link>http://www.medworm.com/index.php?rid=1751374&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18759603%26dopt%3DAbstract</link>
            <description>Ossified pseudomeningocele following Chiari decompression surgery in a patient with Kleeblattsch&amp;#xE4;del deformity.
    J Neurosurg Pediatrics. 2008 Sep;2(3):203-206
    Authors: Reynolds MR, Blackburn SL, Smyth MD
    The authors present the case of a 3-year-old child with Kleeblattsch&amp;#xE4;del, or cloverleaf skull deformity, and a Chiari malformation Type I who developed an ossified pseudomeningocele after posterior fossa decompression. To their knowledge, this is the first report of a postoperative ossified pseudomeningocele in a patient with Kleeblattsch&amp;#xE4;del and the only case of an ossified pseudomeningocele located outside the lumbosacral region. A genetic basis for the ossification process seems likely given the child's history of premature cranial suture closure. The authors d...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1751374</comments>
            <pubDate>Mon, 01 Sep 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1751374</guid>        </item>
        <item>
            <title>Isolated origin of the left internal carotid artery from the pulmonary artery.</title>
            <link>http://www.medworm.com/index.php?rid=1751373&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18759604%26dopt%3DAbstract</link>
            <description>Authors: Hurley MC, Nguyen PH, Dipatri AJ, Shaibani A
    The authors describe what is, to their knowledge, the first reported case of the anomalous origin of an internal carotid artery from the pulmonary artery. An otherwise asymptomatic 6-year-old girl, who presented with headaches and hypertension, underwent a comprehensive workup that revealed extensive meningeal and cerebral artery anastomoses to the left internal carotid artery-itself arising from the origin of the left pulmonary artery. This unique anatomical anomaly, caused by a disturbed pattern of aortic arch regression, resulted in a right-to-left vascular shunt into the pulmonary artery and a disturbance of intracranial artery flow patterns, complicating the management options.
    PMID: 18759604 [PubMed - as supplied by publis...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1751373</comments>
            <pubDate>Mon, 01 Sep 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1751373</guid>        </item>
        <item>
            <title>Rapid progression of hypothyroidism-related pituitary hyperplasia.</title>
            <link>http://www.medworm.com/index.php?rid=1751372&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18759605%26dopt%3DAbstract</link>
            <description>Authors: Lee CY, Hsu HH, Lai HY, Lee ST
    Sellar and suprasellar masses are related to many factors. The authors report on a 10.3-year-old female patient who presented with growth retardation. Initial normal results of a hormone study and rapid progression of hypothyroidism-related pituitary hyperplasia within a 4-week interval were noted. The mass disappeared after thyroxine treatment. The authors conclude that repeated hormone examinations and avoidance of an unnecessary operation are needed in such patients.
    PMID: 18759605 [PubMed - as supplied by publisher] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1751372</comments>
            <pubDate>Mon, 01 Sep 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1751372</guid>        </item>
        <item>
            <title>Primary primitive neuroectodermal tumor of the lumbar extradural space.</title>
            <link>http://www.medworm.com/index.php?rid=1751371&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18759606%26dopt%3DAbstract</link>
            <description>Authors: Ozdemir N, Usta G, Minoglu M, Erbay AM, Bezircioglu H, Tunakan M
    Primary spinal primitive neuroectodermal tumors (PNETs) of the extradural space are very rare; only 10 cases have been reported in the English language literature. The histopathological diagnosis of primary spinal PNETs has been discussed for many years. These tumors have a rapidly progressive course, and there is no current consensus on the optimal therapeutic approach for these patients. The authors present a case of primary PNET located in the lumbar extradural space in a 13-year-old girl and report the clinical, radiological, histopathological, and surgical findings. They compare their findings with those from the other 10 cases reported in the literature and review relevant literature.
    PMID: 18759606 [Pu...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1751371</comments>
            <pubDate>Mon, 01 Sep 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1751371</guid>        </item>
        <item>
            <title>Magnetic field interactions in adjustable hydrocephalus shunts.</title>
            <link>http://www.medworm.com/index.php?rid=1751370&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18759607%26dopt%3DAbstract</link>
            <description>Conclusions All valves, with the exception of the Polaris and ProGAV models, are prone to unintentional reprogramming when exposed to heterogeneous magnetic fields stronger than 40 mT. All tested valves can be considered safe for 3-T MR imaging. All valves generated a distortion of the MR image, especially the GE sequences.
    PMID: 18759607 [PubMed - as supplied by publisher] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1751370</comments>
            <pubDate>Mon, 01 Sep 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1751370</guid>        </item>
        <item>
            <title>Gamma Knife Surgery and Arteriovenous Malformations.</title>
            <link>http://www.medworm.com/index.php?rid=1751369&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18759608%26dopt%3DAbstract</link>
            <description>Authors: Buis DR, Vandertop WP
    
    PMID: 18759608 [PubMed - as supplied by publisher] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1751369</comments>
            <pubDate>Mon, 01 Sep 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1751369</guid>        </item>
        <item>
            <title>Extracranial traumatic carotid artery dissections in children.</title>
            <link>http://www.medworm.com/index.php?rid=1675734&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18671612%26dopt%3DAbstract</link>
            <description>Authors: Rosenwasser RH
    
    PMID: 18671612 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1675734</comments>
            <pubDate>Fri, 01 Aug 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1675734</guid>        </item>
        <item>
            <title>Extracranial traumatic carotid artery dissections in children: a review of current diagnosis and treatment options.</title>
            <link>http://www.medworm.com/index.php?rid=1675733&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18671613%26dopt%3DAbstract</link>
            <description>Conclusions As a result of this review of the literature, the authors propose the algorithms for the evaluation and treatment of traumatic extracranial CADs in children. These recommendations include utilizing MR angiography as a screening tool in cases in which the clinical suspicion of CAD is high, using conventional cerebral angiography to confirm the diagnosis, implementing antiplatelet therapy as initial medical management, and reserving endovascular stenting in cases of failed medical treatment.
    PMID: 18671613 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1675733</comments>
            <pubDate>Fri, 01 Aug 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1675733</guid>        </item>
        <item>
            <title>It's randomized and double blinded... what more do we want?</title>
            <link>http://www.medworm.com/index.php?rid=1675732&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18671614%26dopt%3DAbstract</link>
            <description>Authors: Kestle JR
    
    PMID: 18671614 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1675732</comments>
            <pubDate>Fri, 01 Aug 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1675732</guid>        </item>
        <item>
            <title>Antimicrobial suture wound closure for cerebrospinal fluid shunt surgery: a prospective, double-blinded, randomized controlled trial.</title>
            <link>http://www.medworm.com/index.php?rid=1675731&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18671615%26dopt%3DAbstract</link>
            <description>Conclusions These results support the suggestion that the use of AMS for CSF shunt surgery wound closure is safe, effective, and may be associated with a reduced risk of postoperative shunt infection. A larger randomized controlled trial is needed to confirm this association.
    PMID: 18671615 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1675731</comments>
            <pubDate>Fri, 01 Aug 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1675731</guid>        </item>
        <item>
            <title>Germ cell tumors in the basal ganglia: problems of early diagnosis and treatment.</title>
            <link>http://www.medworm.com/index.php?rid=1675730&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18671616%26dopt%3DAbstract</link>
            <description>Conclusions Early diagnosis requires MR imaging with administration of contrast medium in young patients presenting with motor weakness and/or precocious puberty. Serial neuroimaging studies should be performed if any tiny lesion is detected in the basal ganglia. Since insufficient treatment resulted in early recurrence, radiation therapy with adequate dose and field is essential.
    PMID: 18671616 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1675730</comments>
            <pubDate>Fri, 01 Aug 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1675730</guid>        </item>
        <item>
            <title>Use of thalidomide to diminish growth velocity in a life-threatening congenital intracranial hemangioma.</title>
            <link>http://www.medworm.com/index.php?rid=1675729&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18671617%26dopt%3DAbstract</link>
            <description>Authors: Frei-Jones M, McKinstry RC, Perry A, Leonard JR, Park TS, Rubin JB
    Infantile or capillary hemangioma is the most common vascular tumor of childhood. The tumors most frequently affect the head and neck area, but rare cases of intracranial lesions have been reported. Their natural history is marked by initial rapid growth velocity followed by a plateau and, in most cases, subsequent involution. Although the lesions are considered benign, 10% of affected children develop life-threatening complications (mortality rate 20-80% in this subgroup). When surgical intervention or other methods of local control are not possible, therapeutic options are limited. Corticosteroids have been the mainstay of therapy but therapeutic response is not predictable and the infectious risk is not negl...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1675729</comments>
            <pubDate>Fri, 01 Aug 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1675729</guid>        </item>
        <item>
            <title>Glossopharyngeal schwannoma in childhood.</title>
            <link>http://www.medworm.com/index.php?rid=1675728&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18671618%26dopt%3DAbstract</link>
            <description>Authors: Thomas JA, Bank WO, Myseros JS
    Glossopharyngeal (that is, cranial nerve IX) schwannomas are extremely rare nerve sheath tumors that frequently mimic the more common vestibular schwannoma in their clinical as well as radiographic presentation. Although rare in adults, this tumor has not been reported in a child. The authors report the case of a 10-year-old boy who presented with several months of unilateral hearing loss. He was found to have a large right cerebellopontine angle tumor. Given the boy's primary complaint of hearing loss and the appearance of the lesion on imaging, the tumor was initially believed to be a schwannoma of the vestibular nerve. It was found intraoperatively, however, to originate from the glossopharyngeal nerve. To the authors' knowledge, this is the f...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1675728</comments>
            <pubDate>Fri, 01 Aug 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1675728</guid>        </item>
        <item>
            <title>Unilateral partial hemilaminectomy for disc removal in a 1-year-old child.</title>
            <link>http://www.medworm.com/index.php?rid=1675727&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18671619%26dopt%3DAbstract</link>
            <description>Authors: Benifla M, Melamed I, Barrelly R, Aloushin A, Shelef I
    Intravertebral disc herniation is common in adults, often due to degenerative processes. The occurrence of disc herniation is rare in children and is usually related to traumatic injury. The authors present an unusual case of a 13-month-old boy with L5-S1 lumbar disc herniation. The disc was removed via a unilateral partial hemilaminectomy approach, sparing the spinal midline structural elements. Although rare, lumbar disc herniation should be in the differential diagnosis for children presenting with low-back pain and/or neurological deficit of the lower limbs.
    PMID: 18671619 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1675727</comments>
            <pubDate>Fri, 01 Aug 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1675727</guid>        </item>
        <item>
            <title>Foramen magnum stenosis from overgrowth of the opisthion in a child with achondroplasia.</title>
            <link>http://www.medworm.com/index.php?rid=1675726&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18671620%26dopt%3DAbstract</link>
            <description>Authors: Jha RM, Klimo P, Smith ER
    Achondroplasia has a known association with foramen magnum stenosis that can result in cervicomedullary compression, which is most often due to a hypertrophied posterior occipital rim and an undersized transverse diameter. The authors present a unique case of a child with achondroplasia with symptomatic craniocervical compression from marked overgrowth of his opisthion anterior to the posterior arch of the atlas. This 22-month-old child with achondroplasia presented with severe respiratory and motor disabilities, including progressive quadriparesis and apneic episodes requiring continuous positive airway pressure. Magnetic resonance imaging and CT scans revealed marked foramen magnum stenosis from overgrowth of the opisthion, a hypoplastic C-1 ring, a...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1675726</comments>
            <pubDate>Fri, 01 Aug 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1675726</guid>        </item>
        <item>
            <title>Thoracolumbar spine subdural hematoma as a result of nonaccidental trauma in a 4-month-old infant.</title>
            <link>http://www.medworm.com/index.php?rid=1675725&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18671621%26dopt%3DAbstract</link>
            <description>Authors: Gruber TJ, Rozzelle CJ
    The authors describe the previously unreported occurrence of thoracolumbar subdural hematoma (SDH) resulting from nonaccidental trauma and emphasize the need for a complete and thorough neurological, physical, and radiological examination in all cases of suspected nonaccidental trauma. A 4-month-old male infant presented to the authors' Level 1 pediatric trauma center in respiratory arrest. According to the family, he had been previously healthy with a 1-day history of fussiness and irritability. While with one of the parents, the patient was noted to be apneic and had been shaken in 2 separate episodes in an attempt to stimulate respiration. Emergency services personnel intubated the child's trachea and transported him to the hospital. On arrival in the...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1675725</comments>
            <pubDate>Fri, 01 Aug 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1675725</guid>        </item>
        <item>
            <title>Dialysis disequilibrium syndrome: a consideration in patients with hydrocephalus.</title>
            <link>http://www.medworm.com/index.php?rid=1675724&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18671622%26dopt%3DAbstract</link>
            <description>Authors: Flannery T, Shoakazemi A, McLaughlin B, Woodman A, Cooke S
    Dialysis disequilibrium syndrome is a rare neurological manifestation of intermittent hemodialysis. Urea removal occurs more slowly across the blood-brain barrier than from the plasma, generating an osmotic gradient that promotes water movement into the brain and cerebral edema. The authors report the development of dialysis disequilibrium syndrome in a patient with spina bifida and an adequately functioning shunt.
    PMID: 18671622 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1675724</comments>
            <pubDate>Fri, 01 Aug 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1675724</guid>        </item>
        <item>
            <title>Anatomic hemispherectomy for intractable epilepsy in a patient with unilateral schizencephaly.</title>
            <link>http://www.medworm.com/index.php?rid=1675723&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18671623%26dopt%3DAbstract</link>
            <description>Authors: Heuer GG, Hardesty DA, Zaghloul KA, Simon Schwartz EM, Foley AR, Storm PB
    Schizencephaly is a rare congenital cortical brain malformation defined by unilateral or bilateral clefts of the cerebral hemispheres. These malformations are often associated with medically intractable epilepsy. Surgical solutions include lesionectomy, lobectomy, or hemispherectomy. The authors describe the case of an anatomic hemispherectomy for medically intractable epilepsy in an 8-year-old boy with a large schizencephalic cleft. Seven years prior to his epilepsy surgery, the patient underwent placement of a ventriculoperitoneal shunt for communicating hydrocephalus that resulted in severe left-to-right shift. Subsequently, medically refractory epilepsy developed and the patient underwent an anatomic...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1675723</comments>
            <pubDate>Fri, 01 Aug 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1675723</guid>        </item>
        <item>
            <title>Vascular and apoptotic changes in the placode of myelomeningocele mice during the final stages of in utero development.</title>
            <link>http://www.medworm.com/index.php?rid=1675722&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18671624%26dopt%3DAbstract</link>
            <description>Conclusions Fetal placodes in MMC mice showed evidence of increased vascular density since embryonic Day 16.5 and increased apoptosis at embryonic Day 18.5. These new data support the view that in utero changes of the MMC placode, occurring during the last stages of gestation, contribute to the neuropathological manifestations in full-term newborns with MMC.
    PMID: 18671624 [PubMed - as supplied by publisher] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1675722</comments>
            <pubDate>Fri, 01 Aug 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1675722</guid>        </item>
        <item>
            <title>Moyamoya.</title>
            <link>http://www.medworm.com/index.php?rid=1675721&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18671625%26dopt%3DAbstract</link>
            <description>Authors: Scott RM
    
    PMID: 18671625 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1675721</comments>
            <pubDate>Fri, 01 Aug 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1675721</guid>        </item>
        <item>
            <title>Combined endoscopy-assisted cranionasal approach for resection of infantile myofibromatosis of the ethmoid and anterior skull base. Case report.</title>
            <link>http://www.medworm.com/index.php?rid=1665764&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18590397%26dopt%3DAbstract</link>
            <description>Authors: Galassi E, Pasquini E, Frank G, Marucci G
    The advent and widespread development of endonasal endoscopic techniques have recently expanded the frontiers of skull base surgery. The reduced invasiveness, wider and adjustable visualization of the operative field, and lack of postoperative cosmetic defects are well-known advantages of the endonasal endoscopic approaches compared with traditional surgical exposures both in adults and in children. The need to avoid disruption of facial growth centers and permanent tooth roots represents a further special consideration in favor of these endoscopic techniques in children. The authors report on a case of solitary myofibroma involving the ethmoid, mesial orbits, and anterior skull base with intracranial intradural expansion in a 17-month...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1665764</comments>
            <pubDate>Tue, 01 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1665764</guid>        </item>
        <item>
            <title>Surgical management of the Chiari malformation Type I: the way forward.</title>
            <link>http://www.medworm.com/index.php?rid=1607463&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18590395%26dopt%3DAbstract</link>
            <description>Authors: Piatt JH
    
    PMID: 18590395 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1607463</comments>
            <pubDate>Tue, 01 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1607463</guid>        </item>
        <item>
            <title>Extraventricular neurocytoma in neurofibromatosis Type 1: case report.</title>
            <link>http://www.medworm.com/index.php?rid=1607462&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18590398%26dopt%3DAbstract</link>
            <description>Authors: Raja AI, Yeaney GA, Jakacki RI, Hamilton RL, Pollack IF
    Neurocytomas are rare tumors of the central nervous system that are typically located in the ventricular system. The authors report a case of a child with neurofibromatosis Type 1 (NF1) who had a tumor of the optic nerves and chiasm with signal abnormality extending through the diencephalon, as well as an occipital lobe mass, which was presumed to be part of the visual pathway neoplasm. Because the occipital lobe lesion slowly increased in size over time, while the other areas remained stable, a biopsy was performed. Pathological evaluation revealed an extraventricular neurocytoma of extraventricular neurocytoma. To the authors' knowledge, neurocytomas have not been previously reported in patients with NF1. Because visual...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1607462</comments>
            <pubDate>Tue, 01 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1607462</guid>        </item>
        <item>
            <title>Ventriculoatrial shunt catheter displacement in a child with partial anomalous pulmonary venous return: case report.</title>
            <link>http://www.medworm.com/index.php?rid=1607461&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18590399%26dopt%3DAbstract</link>
            <description>Authors: Elhammady MS, Benglis DM, Bhatia S, Sandberg DI, Ragheb J
    Ventriculoatrial (VA) shunts remain the most used alternative to ventriculoperitoneal shunts in infants with hydrocephalus. The authors report a case of an acute VA shunt malfunction as a result of distal catheter displacement in an 18-month-old girl with partial anomalous pulmonary venous return. The child presented with respiratory compromise, and a chest radiograph revealed a lung infiltrate and normal position of the distal shunt catheter tip. Computed tomography demonstrated stable ventricle size in comparison with previous studies. As the patient's respiratory distress progressed, she required intubation, mechanical ventilation with high airway pressures and inspired oxygen concentrations, muscle relaxants, and se...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1607461</comments>
            <pubDate>Tue, 01 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1607461</guid>        </item>
        <item>
            <title>Retrieval of ventricular catheter with the aid of endoscopy: technical note.</title>
            <link>http://www.medworm.com/index.php?rid=1607460&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18590400%26dopt%3DAbstract</link>
            <description>Authors: Pettorini BL, Frassanito P, Tamburrini G, Massimi L, Caldarelli M, Di Rocco C
    Multilocular hydrocephalus usually requires placement of multiple ventricular catheters for the treatment of secondary cysts and intraventricular septation. The formation of strong adhesions can embed the catheters so that they cannot be removed without a higher risk of intraventricular hemorrhage. Moreover, the devices could represent a nidus for infection and a risk for formation and enlargement of intraventricular secondary cysts. Neuroendoscopy allows the surgeon safely to reach the ventricular catheters that have been left or lost in the ventricular cavity, and to remove them via a minimally invasive approach. In this paper, the authors document another application of ventricular endoscopy in th...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1607460</comments>
            <pubDate>Tue, 01 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1607460</guid>        </item>
        <item>
            <title>Quantitative diffusion tensor imaging and intellectual outcomes in spina bifida: laboratory investigation.</title>
            <link>http://www.medworm.com/index.php?rid=1607459&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18590401%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: Diffusion tensor imaging-derived metrics provide noninvasive neuronal surrogate markers of the pathogenesis of SB and predict variations in general intellectual outcomes in children with this condition.
    PMID: 18590401 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1607459</comments>
            <pubDate>Tue, 01 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1607459</guid>        </item>
        <item>
            <title>Intracranial pressure waves: characterization of a pulsation absorber with notch filter properties using systems analysis: laboratory investigation.</title>
            <link>http://www.medworm.com/index.php?rid=1607458&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18590402%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: The intracranial system in these animals could be considered to include a pulsation absorber for which the target frequency appears to be close to the cardiac frequency. One possible source for such an absorber mechanism might be the free movement of cerebrospinal fluid, implying that impairment of this motion may have important clinical implications in various neurological conditions such as hydrocephalus.
    PMID: 18590402 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1607458</comments>
            <pubDate>Tue, 01 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1607458</guid>        </item>
        <item>
            <title>The importance of the cortical subarachnoid space in understanding hydrocephalus.</title>
            <link>http://www.medworm.com/index.php?rid=1570386&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18590387%26dopt%3DAbstract</link>
            <description>Conclusions The important role of the CSAS in the pathophysiology of various forms of hydrocephalus has been largely ignored. Attention to the dynamics of the CSF in this compartment will improve understanding of enigmatic conditions of hydrocephalus and improve selection criteria for treatment paradigms such as ETV. These concepts lead to clearly defined problems that may be solved by the creation of a central database to address these issues.
    PMID: 18590387 [PubMed - as supplied by publisher] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1570386</comments>
            <pubDate>Tue, 01 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1570386</guid>        </item>
        <item>
            <title>Hydrocephalus and adjustable valves.</title>
            <link>http://www.medworm.com/index.php?rid=1570385&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18590388%26dopt%3DAbstract</link>
            <description>Authors: Rekate HL
    
    PMID: 18590388 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1570385</comments>
            <pubDate>Tue, 01 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1570385</guid>        </item>
        <item>
            <title>Management of hydrocephalus in infants by using shunts with adjustable valves.</title>
            <link>http://www.medworm.com/index.php?rid=1570384&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18590389%26dopt%3DAbstract</link>
            <description>Conclusions The adjustable differential-pressure valve used in this study was not effective in preventing slitlike ventricles in the majority of patients. Despite the small number of patients, this study provides a rationale for examining whether new shunt designs (gravitational shunt valves) are superior to conventional shunt systems in managing challenging hydrocephalus problems.
    PMID: 18590389 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1570384</comments>
            <pubDate>Tue, 01 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1570384</guid>        </item>
        <item>
            <title>Concurrent use of a lumboperitoneal shunt with programmable valve and ventricular access device in the treatment of pseudotumor cerebri: review of 40 cases.</title>
            <link>http://www.medworm.com/index.php?rid=1570383&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18590390%26dopt%3DAbstract</link>
            <description>Conclusions Lumboperitoneal shunts with programmable valves effectively controlled the outflow of lumbar cerebrospinal fluid to ameliorate the symptoms of PTC. The VAD permitted assessment of ICP and thus, indirectly, LP shunt function, and benefits outweighed risks. The programmable valve permitted cerebrospinal fluid flow to be adjusted based on patients' clinical status and ICP to be measured by the VAD.
    PMID: 18590390 [PubMed - as supplied by publisher] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1570383</comments>
            <pubDate>Tue, 01 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1570383</guid>        </item>
        <item>
            <title>Efficacy of intraoperative wound irrigation for preventing shunt infection.</title>
            <link>http://www.medworm.com/index.php?rid=1570382&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18590391%26dopt%3DAbstract</link>
            <description>Conclusions Use of an irrigation strategy aimed at reducing bacteria from the operating field and wound can be considered an effective procedure for preventing shunt infection.
    PMID: 18590391 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1570382</comments>
            <pubDate>Tue, 01 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1570382</guid>        </item>
        <item>
            <title>Changing the paradigm of 1-stage total callosotomy for the treatment of pediatric generalized epilepsy.</title>
            <link>http://www.medworm.com/index.php?rid=1570381&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18590392%26dopt%3DAbstract</link>
            <description>Conclusions For pediatric generalized epilepsy syndrome, 1-stage total callosotomy will be the first choice in treatment for controlling generalized seizures.
    PMID: 18590392 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1570381</comments>
            <pubDate>Tue, 01 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1570381</guid>        </item>
        <item>
            <title>Effect of preoperative skull block on pediatric moyamoya disease.</title>
            <link>http://www.medworm.com/index.php?rid=1570380&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18590393%26dopt%3DAbstract</link>
            <description>Conclusions The use of skull block during EDAMS surgery provided easy hemodynamic control, calm awakening, and better pain relief and may be related to the reduced postoperative morbidity.
    PMID: 18590393 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1570380</comments>
            <pubDate>Tue, 01 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1570380</guid>        </item>
        <item>
            <title>Comparison of posterior fossa decompression with and without duraplasty for the surgical treatment of Chiari malformation Type I in pediatric patients: a meta-analysis.</title>
            <link>http://www.medworm.com/index.php?rid=1570379&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18590394%26dopt%3DAbstract</link>
            <description>Conclusions Posterior fossa decompression with duraplasty is associated with a lower risk of reoperation than PFD but a greater risk for cerebrospinal fluid-related complications. There was no significant difference between the 2 operative techniques with respect to clinical improvement or decrease in syringomyelia.
    PMID: 18590394 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1570379</comments>
            <pubDate>Tue, 01 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1570379</guid>        </item>
        <item>
            <title>Surgical management of the Chiari malformation Type I-the way forward.</title>
            <link>http://www.medworm.com/index.php?rid=1570378&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18590395%26dopt%3DAbstract</link>
            <description>Authors: Piatt JH
    
    PMID: 18590395 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1570378</comments>
            <pubDate>Tue, 01 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1570378</guid>        </item>
        <item>
            <title>Intraoperative ultrasonography as a guide to patient selection for duraplasty after suboccipital decompression in children with Chiari malformation Type I.</title>
            <link>http://www.medworm.com/index.php?rid=1570377&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18590396%26dopt%3DAbstract</link>
            <description>Conclusions In the setting of moderate-to-severe tonsillar CM-I, intraoperative ultrasonography demonstrating decompression of the subarachnoid spaces ventral and dorsal to the tonsils may not effectively select patients in whom bone decompression alone is sufficient. Duraplasty may be warranted in cases of tonsillar herniation that extends below the C-1 lamina regardless of intraoperative ultrasonography findings. More objective cerebrospinal fluid flow or volumetric measures may be needed intraoperatively to guide duraplasty in patients with more pronounced tonsillar herniation.
    PMID: 18590396 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1570377</comments>
            <pubDate>Tue, 01 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1570377</guid>        </item>
        <item>
            <title>Combined endoscopy-assisted cranionasal approach for resection of infantile myofibromatosis of the ethmoid and anterior skull base.</title>
            <link>http://www.medworm.com/index.php?rid=1570376&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18590397%26dopt%3DAbstract</link>
            <description>Authors: Galassi E, Pasquini E, Frank G, Marucci G
    The advent and widespread development of endonasal endoscopic techniques have recently expanded the frontiers of skull base surgery. The reduced invasiveness, wider and adjustable visualization of the operative field, and lack of postoperative cosmetic defects are well-known advantages of the endonasal endoscopic approaches compared with traditional surgical exposures both in adults and in children. The need to avoid disruption of facial growth centers and permanent tooth roots represents a further special consideration in favor of these endoscopic techniques in children. The authors report on a case of solitary myofibroma involving the ethmoid, mesial orbits, and anterior skull base with intracranial intradural expansion in a 17-month...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1570376</comments>
            <pubDate>Tue, 01 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1570376</guid>        </item>
        <item>
            <title>Extraventricular neurocytoma in neurofibromatosis Type 1.</title>
            <link>http://www.medworm.com/index.php?rid=1570375&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18590398%26dopt%3DAbstract</link>
            <description>Authors: Raja AI, Yeaney GA, Jakacki RI, Hamilton RL, Pollack IF
    Neurocytomas are rare tumors of the central nervous system that are typically located in the ventricular system. The authors report a case of a child with neurofibromatosis Type 1 (NF1) who had a tumor of the optic nerves and chiasm with signal abnormality extending through the diencephalon, as well as an occipital lobe mass, which was presumed to be part of the visual pathway neoplasm. Because the occipital lobe lesion slowly increased in size over time, while the other areas remained stable, a biopsy was performed. Pathological evaluation revealed an extraventricular neurocytoma of extraventricular neurocytoma. To the authors' knowledge, neurocytomas have not been previously reported in patients with NF1. Because visual...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1570375</comments>
            <pubDate>Tue, 01 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1570375</guid>        </item>
        <item>
            <title>Ventriculoatrial shunt catheter displacement in a child with partial anomalous pulmonary venous return.</title>
            <link>http://www.medworm.com/index.php?rid=1570374&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18590399%26dopt%3DAbstract</link>
            <description>Authors: Elhammady MS, Benglis DM, Bhatia S, Sandberg DI, Ragheb J
    Ventriculoatrial (VA) shunts remain the most used alternative to ventriculoperitoneal shunts in infants with hydrocephalus. The authors report a case of an acute VA shunt malfunction as a result of distal catheter displacement in an 18-month-old girl with partial anomalous pulmonary venous return. The child presented with respiratory compromise, and a chest radiograph revealed a lung infiltrate and normal position of the distal shunt catheter tip. Computed tomography demonstrated stable ventricle size in comparison with previous studies. As the patient's respiratory distress progressed, she required intubation, mechanical ventilation with high airway pressures and inspired oxygen concentrations, muscle relaxants, and se...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1570374</comments>
            <pubDate>Tue, 01 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1570374</guid>        </item>
        <item>
            <title>Retrieval of ventricular catheter with the aid of endoscopy.</title>
            <link>http://www.medworm.com/index.php?rid=1570373&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18590400%26dopt%3DAbstract</link>
            <description>Authors: Pettorini BL, Frassanito P, Tamburrini G, Massimi L, Caldarelli M, Di Rocco C
    Multilocular hydrocephalus usually requires placement of multiple ventricular catheters for the treatment of secondary cysts and intraventricular septation. The formation of strong adhesions can embed the catheters so that they cannot be removed without a higher risk of intraventricular hemorrhage. Moreover, the devices could represent a nidus for infection and a risk for formation and enlargement of intraventricular secondary cysts. Neuroendoscopy allows the surgeon safely to reach the ventricular catheters that have been left or lost in the ventricular cavity, and to remove them via a minimally invasive approach. In this paper, the authors document another application of ventricular endoscopy in th...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1570373</comments>
            <pubDate>Tue, 01 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1570373</guid>        </item>
        <item>
            <title>Quantitative diffusion tensor imaging and intellectual outcomes in spina bifida.</title>
            <link>http://www.medworm.com/index.php?rid=1570372&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18590401%26dopt%3DAbstract</link>
            <description>Conclusions Diffusion tensor imaging-derived metrics provide noninvasive neuronal surrogate markers of the pathogenesis of SB and predict variations in general intellectual outcomes in children with this condition.
    PMID: 18590401 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1570372</comments>
            <pubDate>Tue, 01 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1570372</guid>        </item>
        <item>
            <title>Intracranial pressure waves: characterization of a pulsation absorber with notch filter properties using systems analysis.</title>
            <link>http://www.medworm.com/index.php?rid=1570371&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18590402%26dopt%3DAbstract</link>
            <description>Conclusions The intracranial system in these animals could be considered to include a pulsation absorber for which the target frequency appears to be close to the cardiac frequency. One possible source for such an absorber mechanism might be the free movement of cerebrospinal fluid, implying that impairment of this motion may have important clinical implications in various neurological conditions such as hydrocephalus.
    PMID: 18590402 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1570371</comments>
            <pubDate>Tue, 01 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1570371</guid>        </item>
        <item>
            <title>Achondroplasia.</title>
            <link>http://www.medworm.com/index.php?rid=1570370&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18590403%26dopt%3DAbstract</link>
            <description>Conclusions Decompression of the spinal canal in pediatric patients with achondroplasia can be accomplished safely with significant clinical benefit. Patients with a history of cervicomedullary compression may be at an increased risk of developing symptomatic stenosis prior to adolescence. Fusion procedures are recommended in patients with a large decompression overlying a thoracolumbar kyphosis to avoid progressive postoperative deformity.
    PMID: 18590403 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1570370</comments>
            <pubDate>Tue, 01 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1570370</guid>        </item>
        <item>
            <title>Manpower issues in pediatric neurosurgery.</title>
            <link>http://www.medworm.com/index.php?rid=1570404&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18518689%26dopt%3DAbstract</link>
            <description>Authors: Rekate HL
    
    PMID: 18518689 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1570404</comments>
            <pubDate>Sun, 01 Jun 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1570404</guid>        </item>
        <item>
            <title>A 15-year review of pediatric neurosurgical fellowships: implications for the pediatric neurosurgical workforce.</title>
            <link>http://www.medworm.com/index.php?rid=1570403&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18518690%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: Although the present training infrastructure has the theoretical capacity to train &amp;gt; 20 pediatric neurosurgeons each year, this analysis suggests that current levels will provide approximately 6 ABPNS-certified pediatric neurosurgeons annually. This raises the question of the sufficiency of the future pediatric neurosurgical workforce.
    PMID: 18518690 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1570403</comments>
            <pubDate>Sun, 01 Jun 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1570403</guid>        </item>
        <item>
            <title>Ventriculoperitoneal shunt tap.</title>
            <link>http://www.medworm.com/index.php?rid=1570402&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18518691%26dopt%3DAbstract</link>
            <description>Authors: Oakes WJ
    
    PMID: 18518691 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1570402</comments>
            <pubDate>Sun, 01 Jun 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1570402</guid>        </item>
        <item>
            <title>Rethinking the indications for the ventriculoperitoneal shunt tap.</title>
            <link>http://www.medworm.com/index.php?rid=1570401&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18518692%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: The authors have shown that it is possible to evaluate the majority of ventricular shunt malfunctions without tapping the device. Because it is possible to diagnose shunt obstruction correctly by other means, the shunt tap may not be obligatory as a routine test of the device's patency.
    PMID: 18518692 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1570401</comments>
            <pubDate>Sun, 01 Jun 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1570401</guid>        </item>
        <item>
            <title>Ventricular shunt tap as a predictor of proximal shunt malfunction in children: a prospective study.</title>
            <link>http://www.medworm.com/index.php?rid=1570400&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18518693%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: Poor flow of CSF on shunt tap is highly predictive of obstruction of the proximal catheter. Because not all patients with good flow on shunt tap underwent surgical shunt exploration, the specificity of this test cannot be determined. Nonetheless, a shunt tap that reveals good flow with a normal opening pressure can be misleading, and management of such cases should be based on clinical judgment.
    PMID: 18518693 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1570400</comments>
            <pubDate>Sun, 01 Jun 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1570400</guid>        </item>
        <item>
            <title>Clinical and economic consequences of antibiotic-impregnated cerebrospinal fluid shunt catheters.</title>
            <link>http://www.medworm.com/index.php?rid=1570399&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18518694%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: From clinical and economic perspectives, AISCs are seemingly a valuable addition in hydrocephalus therapy.
    PMID: 18518694 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1570399</comments>
            <pubDate>Sun, 01 Jun 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1570399</guid>        </item>
        <item>
            <title>Predictive value of preoperative ventricular volume on the need for permanent hydrocephalus treatment immediately after resection of posterior fossa medulloblastomas in children.</title>
            <link>http://www.medworm.com/index.php?rid=1570398&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18518695%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: Preoperative ventricular volume has predictive value for the later need for shunt placement, but in clinical practice this may be difficult to appreciate because all patients have significant hydrocephalus at presentation. The rate of ventricular size reduction in response to tumor excision does not have predictive value because ventricular volume is related to tumor volume. It appears that the removal of cerebellar medulloblastoma converts hydrocephalus from obstructive to communicating, which requires surgical treatment if it exceeds a certain level of cerebrospinal fluid volume.
    PMID: 18518695 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1570398</comments>
            <pubDate>Sun, 01 Jun 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1570398</guid>        </item>
        <item>
            <title>Suboccipital decompression for Chiari malformation-associated scoliosis: risk factors and time course of deformity progression.</title>
            <link>http://www.medworm.com/index.php?rid=1570397&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18518696%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: Over one third of patients with CM-I-associated scoliosis will improve after cervicomedullary decompression alone. Cervicomedullary decompression is a good first-line option, particularly in children with concordant posterior fossa symptoms. Patients presenting with more severe scoliosis (increasing Cobb angle) or scoliosis that crosses the thoracolumbar junction may benefit from earlier orthopedic involvement and should be monitored regularly for curvature progression after cervicomedullary decompression. In cases in which there is a failure of the syrinx to show improvement after suboccipital decompression, the patients are also more likely to develop curvature progression.
    PMID: 18518696 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1570397</comments>
            <pubDate>Sun, 01 Jun 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1570397</guid>        </item>
        <item>
            <title>Prediction of cognitive sequelae based on abnormal computed tomography findings in children following mild traumatic brain injury.</title>
            <link>http://www.medworm.com/index.php?rid=1570396&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18518697%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: Neuropsychological recovery during the 1st year following MTBI is related to the presence of radiographically detectable intracranial pathology. Children with intracranial pathology on acute CT performed more poorly in several cognitive domains when compared with patients whose CT findings were normal or limited to a linear skull fracture. Depending on the presence of preinjury ADHD and concomitant extracranial injury, working memory and visuomotor speed were also diminished in patients whose CT findings revealed complications following MTBI. Computed tomography within 24 hours postinjury appears to be useful for identifying children with an elevated risk for residual neuropsychological changes.
    PMID: 18518697 [PubMed - in process] (Source: Journal of neurosurgery. Pediatr...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1570396</comments>
            <pubDate>Sun, 01 Jun 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1570396</guid>        </item>
        <item>
            <title>Severe brain injury with rupture of the superior sagittal sinus after vacuum extraction birth.</title>
            <link>http://www.medworm.com/index.php?rid=1570395&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18518698%26dopt%3DAbstract</link>
            <description>Authors: Musahl C, Schick U
    Vacuum extraction in nonprogressive labor is a relatively safe procedure. Only a few major complications have been reported in the literature. The authors present a case of severe brain damage with rupture of the sinus after vacuum extraction delivery for which surgical repair of the dural tear and brain prolapse was required.
    PMID: 18518698 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1570395</comments>
            <pubDate>Sun, 01 Jun 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1570395</guid>        </item>
        <item>
            <title>Mediastinal lymphangioma presenting as an acute epidural hematoma.</title>
            <link>http://www.medworm.com/index.php?rid=1570394&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18518699%26dopt%3DAbstract</link>
            <description>Authors: McLoughlin GS, Nuchtern JG, Dauser RC, Sciubba DM, Gokaslan ZL, Wolinsky JP
    Lymphangiomas are benign collections of blind-ended lymphatic and vascular channels. Lesions typically occur in the soft tissues of the head and neck, although any region of the body can be affected. Involvement of the spine is very rare. A complete resection is generally curative. On rare occasions, these tumors are complicated by infection or hemorrhage. The authors present an unusual case of a hemorrhagic lymphangioma in a 1-year-old male child. The lesion originated in the mediastinum and extended into the cervicothoracic epidural space via a neural foramen. This resulted in an acute epidural hematoma and quadriparesis. Emergency decompression resulted in full neurological recovery. This may be the...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1570394</comments>
            <pubDate>Sun, 01 Jun 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1570394</guid>        </item>
        <item>
            <title>Spontaneous third ventriculocisternostomy in an infant with obstructive hydrocephalus.</title>
            <link>http://www.medworm.com/index.php?rid=1570393&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18518700%26dopt%3DAbstract</link>
            <description>Authors: Gallia GL, Teo C
    Spontaneous ventriculocisternostomy, the spontaneous communication between the ventricular system and the subarachnoid space, is rare. The authors report a case of an infant with obstructive hydrocephalus who developed a spontaneous third ventriculocisternostomy. The infant was initially evaluated for progressive ventriculomegaly and increasing head circumference (HC). During follow-up, the patient's HC began to follow percentile lines and magnetic resonance (MR) imaging demonstrated a reduction of the hydrocephalus. Flow-sensitive phase-contrast cine MR images revealed cerebrospinal fluid (CSF) flow through the floor of the third ventricle between the tuber cinereum and the mammillary bodies connecting the ventricular system with the prepontine cistern. Altho...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1570393</comments>
            <pubDate>Sun, 01 Jun 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1570393</guid>        </item>
        <item>
            <title>Obstructive hydrocephalus due to a third ventricular neuroepithelial cyst.</title>
            <link>http://www.medworm.com/index.php?rid=1570392&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18518701%26dopt%3DAbstract</link>
            <description>Authors: Ormond DR, Omeis I, Mohan A, Murali R, Narayan P
    Cysts occupying the third ventricle are rare lesions and may appear as an unusual cause of obstructive hydrocephalus. Various types of lesions occur in this location, and they generally have an arachnoidal, endodermal, or neuroepithelial origin. The authors present a case of acute hydrocephalus following minor trauma in a child due to cerebrospinal fluid outflow obstruction by a third ventricular cyst. Definitive diagnosis of this cystic lesion was possible only with contrast ventriculography and not routine computed tomography or magnetic resonance imaging. The investigation, treatment, and pathological findings are discussed.
    PMID: 18518701 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1570392</comments>
            <pubDate>Sun, 01 Jun 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1570392</guid>        </item>
        <item>
            <title>Nasal encephalocele in a child with Beckwith-Wiedemann syndrome.</title>
            <link>http://www.medworm.com/index.php?rid=1570391&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18518702%26dopt%3DAbstract</link>
            <description>Authors: Broekman ML, Hoving EW, Kho KH, Speleman L, Han KS, Hanlo PW
    Beckwith-Wiedemann syndrome (BWS) is a rare congenital syndrome characterized by gigantism, macroglossia, exophthalmos, postpartum hypoglycemia, and multiple midline defects such as omphalocele. The authors describe, to the best of their knowledge, the first case of a child in whom BWS was diagnosed and who was subsequently treated for a nasal encephalocele. Because the authors believe that this feature might not be an incidental finding in patients with BWS, intranasal masses in these patients should be carefully differentiated, as complications might be severe.
    PMID: 18518702 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1570391</comments>
            <pubDate>Sun, 01 Jun 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1570391</guid>        </item>
        <item>
            <title>Giant intracranial capillary hemangioma associated with enlarged head circumference in a newborn.</title>
            <link>http://www.medworm.com/index.php?rid=1570390&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18518703%26dopt%3DAbstract</link>
            <description>Authors: Daenekindt T, Weyns F, Kho KH, Peuskens D, Engelborghs K, Wuyts J
    The authors describe the case of a patient with an intracranial capillary hemangioma, and they review the recent literature on intracranial capillary hemangiomas with special attention to their differential diagnosis and management. The only sign in this 7-week-old boy was head enlargement. There were no neurological deficits, and imaging revealed a large intracranial lesion in the right temporal fossa. The results of biopsy confirmed the diagnosis, and, after endovascular embolization, the entire lesion was resected. The incidence of intracranial capillary hemangioma is very low but may be underestimated. In the present case, the size of the tumor prompted surgical treatment. The natural behavior of extracrania...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1570390</comments>
            <pubDate>Sun, 01 Jun 2008 04:00:00 +0100</pubDate>
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            <title>Cerebral mycetoma with cranial osteomyelitis.</title>
            <link>http://www.medworm.com/index.php?rid=1570389&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18518704%26dopt%3DAbstract</link>
            <description>Authors: Beeram V, Challa S, Vannemreddy P
    Craniocerebral maduromycetoma is extremely rare. The authors describe a case of maduromycetoma involving the left parietal cortex, bone, and subcutaneous tissue in a young male farm laborer who presented with left parietal scalp swelling that had progressed into a relentlessly discharging sinus. Computed tomography (CT) scanning of his brain revealed osteomyelitis of the parietal bone with an underlying homogeneously enhancing tumor. Intraoperatively, the mass was revealed to be a black lesion involving the bone, dura mater, and underlying cerebral cortex. It was friable and separated from the surrounding brain by a thick gliotic scar. Gross-total excision was performed, and the patient was placed on a 6-week regimen of itraconazole. To the au...</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1570389</comments>
            <pubDate>Sun, 01 Jun 2008 04:00:00 +0100</pubDate>
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            <title>Demographics of abusive head trauma.</title>
            <link>http://www.medworm.com/index.php?rid=1570423&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18447666%26dopt%3DAbstract</link>
            <description>Authors: Duhaime AC
    
    PMID: 18447666 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1570423</comments>
            <pubDate>Thu, 01 May 2008 04:00:00 +0100</pubDate>
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            <title>Demographics of abusive head trauma in the Commonwealth of Pennsylvania.</title>
            <link>http://www.medworm.com/index.php?rid=1570422&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18447667%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: This population-based study of abusive head injuries throughout an entire state adds significantly to the growing knowledge about this condition. The results suggests that families of infants with abusive head injuries have significantly different demographic features compared with the general population, although which of these variables is independently significant cannot be ascertained from this study and require further investigation.
    PMID: 18447667 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1570422</comments>
            <pubDate>Thu, 01 May 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1570422</guid>        </item>
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            <title>Management of lumbar shunt site swelling in children.</title>
            <link>http://www.medworm.com/index.php?rid=1570421&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18447668%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: Lumbar shunt site swelling is predominantly a consequence of pericatheter CSF leakage from the mismatch in the dural opening, which corresponds to the outer diameter of the 14-gauge Tuohy needle and the smaller proximal lumbar catheter. It is best managed by direct repair of the defect through a microsurgical interlaminar approach and recannulation of the dura by using only the stylet of a 14-gauge Tuohy needle.
    PMID: 18447668 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1570421</comments>
            <pubDate>Thu, 01 May 2008 04:00:00 +0100</pubDate>
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            <title>Toward reducing shunt placement rates in patients with myelomeningocele.</title>
            <link>http://www.medworm.com/index.php?rid=1570420&amp;cid=s_37310_153_f&amp;fid=37310&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D18447669%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: Applying more stringent guidelines for shunt placement, permitting moderate ventricular dilation, and accepting some mild increase in ventricular size after myelomeningocele closure has resulted in a reduced rate of shunt placement compared with previous series. The rate is comparable to that reported following in utero closure of myelomeningocele.
    PMID: 18447669 [PubMed - in process] (Source: Journal of neurosurgery. Pediatrics)</description>
            <author>Journal of neurosurgery. Pediatrics</author>
            <type>journals</type>
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            <pubDate>Thu, 01 May 2008 04:00:00 +0100</pubDate>
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