Ectopic thoracic parathyroid adenoma: the thoracic surgeon needs multi-approach skills!
Ann Endocrinol (Paris). 2024 Mar 19:S0003-4266(24)00037-4. doi: 10.1016/j.ando.2024.02.002. Online ahead of print.NO ABSTRACTPMID:38513882 | DOI:10.1016/j.ando.2024.02.002 (Source: Annales d'Endocrinologie)
Source: Annales d'Endocrinologie - March 21, 2024 Category: Endocrinology Authors: Matthieu Thumerel Yaniss Belaroussi Ghoufrane Tlili Magalie Haissaguerre Jacques Jougon Source Type: research

Ectopic thoracic parathyroid adenoma: the thoracic surgeon needs multi-approach skills!
Ann Endocrinol (Paris). 2024 Mar 19:S0003-4266(24)00037-4. doi: 10.1016/j.ando.2024.02.002. Online ahead of print.NO ABSTRACTPMID:38513882 | DOI:10.1016/j.ando.2024.02.002 (Source: Annales d'Endocrinologie)
Source: Annales d'Endocrinologie - March 21, 2024 Category: Endocrinology Authors: Matthieu Thumerel Yaniss Belaroussi Ghoufrane Tlili Magalie Haissaguerre Jacques Jougon Source Type: research

Ectopic thoracic parathyroid adenoma: the thoracic surgeon needs multi-approach skills!
Ann Endocrinol (Paris). 2024 Mar 19:S0003-4266(24)00037-4. doi: 10.1016/j.ando.2024.02.002. Online ahead of print.NO ABSTRACTPMID:38513882 | DOI:10.1016/j.ando.2024.02.002 (Source: Annales d'Endocrinologie)
Source: Annales d'Endocrinologie - March 21, 2024 Category: Endocrinology Authors: Matthieu Thumerel Yaniss Belaroussi Ghoufrane Tlili Magalie Haissaguerre Jacques Jougon Source Type: research

Ectopic thoracic parathyroid adenoma: the thoracic surgeon needs multi-approach skills!
Ann Endocrinol (Paris). 2024 Mar 19:S0003-4266(24)00037-4. doi: 10.1016/j.ando.2024.02.002. Online ahead of print.NO ABSTRACTPMID:38513882 | DOI:10.1016/j.ando.2024.02.002 (Source: Annales d'Endocrinologie)
Source: Annales d'Endocrinologie - March 21, 2024 Category: Endocrinology Authors: Matthieu Thumerel Yaniss Belaroussi Ghoufrane Tlili Magalie Haissaguerre Jacques Jougon Source Type: research

Ectopic thoracic parathyroid adenoma: the thoracic surgeon needs multi-approach skills!
Ann Endocrinol (Paris). 2024 Mar 19:S0003-4266(24)00037-4. doi: 10.1016/j.ando.2024.02.002. Online ahead of print.NO ABSTRACTPMID:38513882 | DOI:10.1016/j.ando.2024.02.002 (Source: Annales d'Endocrinologie)
Source: Annales d'Endocrinologie - March 21, 2024 Category: Endocrinology Authors: Matthieu Thumerel Yaniss Belaroussi Ghoufrane Tlili Magalie Haissaguerre Jacques Jougon Source Type: research

Proceedings of the annual meeting of the European Consortium of Lipodystrophies (ECLip), Pisa, Italy, 28-29 September 2023
Ann Endocrinol (Paris). 2024 Mar 5:S0003-4266(24)00036-2. doi: 10.1016/j.ando.2024.03.002. Online ahead of print.ABSTRACTLipodystrophic syndromes are rare diseases affecting primarily the development or maintenance of the adipose tissue but are also distressing indirectly multiple organs and tissues, causing in most of the cases reduced life expectancy and quality of life. Lipodystrophy syndromes are multifaceted disorders caused by genetic mutations or autoimmune and iatrogenic mechanisms, many subtypes are now recognized and classified but the disease remains remarkably underdiagnosed. The European Consortium of Lipodyst...
Source: Annales d'Endocrinologie - March 7, 2024 Category: Endocrinology Authors: Giovanni Ceccarini Baris Akinci David Araujo-Vilar Marianna Beghini Rebecca J Brown Juan Carrion Tudela Valeria Corradin Bruno Donadille Jose Jerez Ruiz Isabelle Jeru Giovanna Lattanzi Margherita Maffei George David McIlroy Estelle Nob écourt Naca Perez Source Type: research

Position statement on the diagnosis and management of congenital pituitary deficiency in adults: the French National Diagnosis and Treatment Protocol (NDTP)
Ann Endocrinol (Paris). 2024 Mar 5:S0003-4266(24)00035-0. doi: 10.1016/j.ando.2024.03.001. Online ahead of print.ABSTRACTPituitary deficiency, or hypopituitarism, is a rare chronic disease. It is defined by insufficient synthesis of one or more pituitary hormones (growth hormone, TSH, ACTH, LH-FSH, prolactin), whether or not associated with arginine vasopressin deficiency (formerly known as diabetes insipidus). In adult patients, it is usually acquired (notably during childhood), but can also be congenital, due to abnormal pituitary development. The present study focuses on congenital pituitary deficiency in adults, from d...
Source: Annales d'Endocrinologie - March 7, 2024 Category: Endocrinology Authors: S Castets F Albarel A Bachelot G Brun J Bouligand C Briet E Bui Quoc C Cazabat C Chabbert-Buffet S Christin-Maitre C Courtillot T Cuny G De Filippo B Donadille F Illouz I Pellegrini Y Reznik A Saveanu N Teissier P Touraine M C Vantyghem J Vergier J L ége Source Type: research

Proceedings of the annual meeting of the European Consortium of Lipodystrophies (ECLip), Pisa, Italy, 28-29 September 2023
Ann Endocrinol (Paris). 2024 Mar 5:S0003-4266(24)00036-2. doi: 10.1016/j.ando.2024.03.002. Online ahead of print.ABSTRACTLipodystrophic syndromes are rare diseases affecting primarily the development or maintenance of the adipose tissue but are also distressing indirectly multiple organs and tissues, causing in most of the cases reduced life expectancy and quality of life. Lipodystrophy syndromes are multifaceted disorders caused by genetic mutations or autoimmune and iatrogenic mechanisms, many subtypes are now recognized and classified but the disease remains remarkably underdiagnosed. The European Consortium of Lipodyst...
Source: Annales d'Endocrinologie - March 7, 2024 Category: Endocrinology Authors: Giovanni Ceccarini Baris Akinci David Araujo-Vilar Marianna Beghini Rebecca J Brown Juan Carrion Tudela Valeria Corradin Bruno Donadille Jose Jerez Ruiz Isabelle Jeru Giovanna Lattanzi Margherita Maffei George David McIlroy Estelle Nob écourt Naca Perez Source Type: research

Position statement on the diagnosis and management of congenital pituitary deficiency in adults: the French National Diagnosis and Treatment Protocol (NDTP)
Ann Endocrinol (Paris). 2024 Mar 5:S0003-4266(24)00035-0. doi: 10.1016/j.ando.2024.03.001. Online ahead of print.ABSTRACTPituitary deficiency, or hypopituitarism, is a rare chronic disease. It is defined by insufficient synthesis of one or more pituitary hormones (growth hormone, TSH, ACTH, LH-FSH, prolactin), whether or not associated with arginine vasopressin deficiency (formerly known as diabetes insipidus). In adult patients, it is usually acquired (notably during childhood), but can also be congenital, due to abnormal pituitary development. The present study focuses on congenital pituitary deficiency in adults, from d...
Source: Annales d'Endocrinologie - March 7, 2024 Category: Endocrinology Authors: S Castets F Albarel A Bachelot G Brun J Bouligand C Briet E Bui Quoc C Cazabat C Chabbert-Buffet S Christin-Maitre C Courtillot T Cuny G De Filippo B Donadille F Illouz I Pellegrini Y Reznik A Saveanu N Teissier P Touraine M C Vantyghem J Vergier J L ége Source Type: research

Proceedings of the annual meeting of the European Consortium of Lipodystrophies (ECLip), Pisa, Italy, 28-29 September 2023
Ann Endocrinol (Paris). 2024 Mar 5:S0003-4266(24)00036-2. doi: 10.1016/j.ando.2024.03.002. Online ahead of print.ABSTRACTLipodystrophic syndromes are rare diseases affecting primarily the development or maintenance of the adipose tissue but are also distressing indirectly multiple organs and tissues, causing in most of the cases reduced life expectancy and quality of life. Lipodystrophy syndromes are multifaceted disorders caused by genetic mutations or autoimmune and iatrogenic mechanisms, many subtypes are now recognized and classified but the disease remains remarkably underdiagnosed. The European Consortium of Lipodyst...
Source: Annales d'Endocrinologie - March 7, 2024 Category: Endocrinology Authors: Giovanni Ceccarini Baris Akinci David Araujo-Vilar Marianna Beghini Rebecca J Brown Juan Carrion Tudela Valeria Corradin Bruno Donadille Jose Jerez Ruiz Isabelle Jeru Giovanna Lattanzi Margherita Maffei George David McIlroy Estelle Nob écourt Naca Perez Source Type: research

Position statement on the diagnosis and management of congenital pituitary deficiency in adults: the French National Diagnosis and Treatment Protocol (NDTP)
Ann Endocrinol (Paris). 2024 Mar 5:S0003-4266(24)00035-0. doi: 10.1016/j.ando.2024.03.001. Online ahead of print.ABSTRACTPituitary deficiency, or hypopituitarism, is a rare chronic disease. It is defined by insufficient synthesis of one or more pituitary hormones (growth hormone, TSH, ACTH, LH-FSH, prolactin), whether or not associated with arginine vasopressin deficiency (formerly known as diabetes insipidus). In adult patients, it is usually acquired (notably during childhood), but can also be congenital, due to abnormal pituitary development. The present study focuses on congenital pituitary deficiency in adults, from d...
Source: Annales d'Endocrinologie - March 7, 2024 Category: Endocrinology Authors: S Castets F Albarel A Bachelot G Brun J Bouligand C Briet E Bui Quoc C Cazabat C Chabbert-Buffet S Christin-Maitre C Courtillot T Cuny G De Filippo B Donadille F Illouz I Pellegrini Y Reznik A Saveanu N Teissier P Touraine M C Vantyghem J Vergier J L ége Source Type: research

Proceedings of the annual meeting of the European Consortium of Lipodystrophies (ECLip), Pisa, Italy, 28-29 September 2023
Ann Endocrinol (Paris). 2024 Mar 5:S0003-4266(24)00036-2. doi: 10.1016/j.ando.2024.03.002. Online ahead of print.ABSTRACTLipodystrophic syndromes are rare diseases affecting primarily the development or maintenance of the adipose tissue but are also distressing indirectly multiple organs and tissues, causing in most of the cases reduced life expectancy and quality of life. Lipodystrophy syndromes are multifaceted disorders caused by genetic mutations or autoimmune and iatrogenic mechanisms, many subtypes are now recognized and classified but the disease remains remarkably underdiagnosed. The European Consortium of Lipodyst...
Source: Annales d'Endocrinologie - March 7, 2024 Category: Endocrinology Authors: Giovanni Ceccarini Baris Akinci David Araujo-Vilar Marianna Beghini Rebecca J Brown Juan Carrion Tudela Valeria Corradin Bruno Donadille Jose Jerez Ruiz Isabelle Jeru Giovanna Lattanzi Margherita Maffei George David McIlroy Estelle Nob écourt Naca Perez Source Type: research

Position statement on the diagnosis and management of congenital pituitary deficiency in adults: the French National Diagnosis and Treatment Protocol (NDTP)
Ann Endocrinol (Paris). 2024 Mar 5:S0003-4266(24)00035-0. doi: 10.1016/j.ando.2024.03.001. Online ahead of print.ABSTRACTPituitary deficiency, or hypopituitarism, is a rare chronic disease. It is defined by insufficient synthesis of one or more pituitary hormones (growth hormone, TSH, ACTH, LH-FSH, prolactin), whether or not associated with arginine vasopressin deficiency (formerly known as diabetes insipidus). In adult patients, it is usually acquired (notably during childhood), but can also be congenital, due to abnormal pituitary development. The present study focuses on congenital pituitary deficiency in adults, from d...
Source: Annales d'Endocrinologie - March 7, 2024 Category: Endocrinology Authors: S Castets F Albarel A Bachelot G Brun J Bouligand C Briet E Bui Quoc C Cazabat C Chabbert-Buffet S Christin-Maitre C Courtillot T Cuny G De Filippo B Donadille F Illouz I Pellegrini Y Reznik A Saveanu N Teissier P Touraine M C Vantyghem J Vergier J L ége Source Type: research

Proceedings of the annual meeting of the European Consortium of Lipodystrophies (ECLip), Pisa, Italy, 28-29 September 2023
Ann Endocrinol (Paris). 2024 Mar 5:S0003-4266(24)00036-2. doi: 10.1016/j.ando.2024.03.002. Online ahead of print.ABSTRACTLipodystrophic syndromes are rare diseases affecting primarily the development or maintenance of the adipose tissue but are also distressing indirectly multiple organs and tissues, causing in most of the cases reduced life expectancy and quality of life. Lipodystrophy syndromes are multifaceted disorders caused by genetic mutations or autoimmune and iatrogenic mechanisms, many subtypes are now recognized and classified but the disease remains remarkably underdiagnosed. The European Consortium of Lipodyst...
Source: Annales d'Endocrinologie - March 7, 2024 Category: Endocrinology Authors: Giovanni Ceccarini Baris Akinci David Araujo-Vilar Marianna Beghini Rebecca J Brown Juan Carrion Tudela Valeria Corradin Bruno Donadille Jose Jerez Ruiz Isabelle Jeru Giovanna Lattanzi Margherita Maffei George David McIlroy Estelle Nob écourt Naca Perez Source Type: research

Position statement on the diagnosis and management of congenital pituitary deficiency in adults: the French National Diagnosis and Treatment Protocol (NDTP)
Ann Endocrinol (Paris). 2024 Mar 5:S0003-4266(24)00035-0. doi: 10.1016/j.ando.2024.03.001. Online ahead of print.ABSTRACTPituitary deficiency, or hypopituitarism, is a rare chronic disease. It is defined by insufficient synthesis of one or more pituitary hormones (growth hormone, TSH, ACTH, LH-FSH, prolactin), whether or not associated with arginine vasopressin deficiency (formerly known as diabetes insipidus). In adult patients, it is usually acquired (notably during childhood), but can also be congenital, due to abnormal pituitary development. The present study focuses on congenital pituitary deficiency in adults, from d...
Source: Annales d'Endocrinologie - March 7, 2024 Category: Endocrinology Authors: S Castets F Albarel A Bachelot G Brun J Bouligand C Briet E Bui Quoc C Cazabat C Chabbert-Buffet S Christin-Maitre C Courtillot T Cuny G De Filippo B Donadille F Illouz I Pellegrini Y Reznik A Saveanu N Teissier P Touraine M C Vantyghem J Vergier J L ége Source Type: research