Search research articles
Contact Us
Filters
Showing results (131-140 of 156) with videos related to
Page
of 16
Sort By:
Clinical Genetics
|
April 1, 2024
Shifting the landscape: Dominant C-terminal rare missense FOXL2 variants in non-syndromic primary ovarian failure etiology
Pénélope Jordan, Camille Verebi, Bérénice Hervé, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 14, 2015
Pregnancy in Women Previously Treated for an Adrenocortical Carcinoma
Pauline de Corbière, Katrin Ritzel, Laure Cazabat, et al.
Human Genetics
|
May 14, 2020
Genomic sequencing highlights the diverse molecular causes of Perrault syndrome: a peroxisomal disorder (PEX6), metabolic disorders (CLPP, GGPS1), and mtDNA maintenance/translation disorders (LARS2, TFAM)
Elena J Tucker, Rocio Rius, Sylvie Jaillard, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists
|
July 4, 2026
Early Metabolic Risk in Childhood Brain Cancer Survivors with Childhood-Onset Growth Hormone Deficiency
Alice Casiraghi, Olivier Pollé, Clément Bailly, et al.
The Journal of Clinical Endocrinology and Metabolism
|
August 1, 2014
The prevalence of CHD7 missense versus truncating mutations is higher in patients with Kallmann syndrome than in typical CHARGE patients
Séverine Marcos, Julie Sarfati, Chrystel Leroy, et al.
The Journal of Clinical Endocrinology and Metabolism
|
August 31, 2016
Gain-of-function Prolactin Receptor Variants Are Not Associated With Breast Cancer and Multiple Fibroadenoma Risk
Zeina Chakhtoura, Fatima Laki, Marie Bernadet, et al.
Annales D'Endocrinologie
|
March 7, 2024
Position statement on the diagnosis and management of congenital pituitary deficiency in adults: The French National Diagnosis and Treatment Protocol (NDTP)
Sarah Castets, Frédérique Albarel, Anne Bachelot, et al.
European Journal of Endocrinology
|
February 18, 2026
European Society for Paediatric Endocrinology (ESPE) and European Society of Endocrinology (ESE) joint clinical practice guidance for healthcare transition from paediatric to adult endocrine care
Enora Le Roux, Kirstine Stochholm, Martin Fassnacht, et al.
Hormone Research in Paediatrics
|
February 19, 2026
European Society for Paediatric Endocrinology and European Society of Endocrinology Joint Clinical Practice Guidance for Healthcare Transition from Paediatric to Adult Endocrine Care
Enora Le Roux, Kirstine Stochholm, Martin Fassnacht, et al.
Endocrine Reviews
|
May 7, 2021
Congenital Adrenal Hyperplasia-Current Insights in Pathophysiology, Diagnostics, and Management
Hedi L Claahsen-van der Grinten, Phyllis W Speiser, S Faisal Ahmed, et al.
Page
of 16
Search research articles
Search
Showing results (131-140 of 156) with videos related to
Sort By:
Page
of 16
Clinical Genetics
|
April 1, 2024
Shifting the landscape: Dominant C-terminal rare missense FOXL2 variants in non-syndromic primary ovarian failure etiology
Pénélope Jordan, Camille Verebi, Bérénice Hervé, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 14, 2015
Pregnancy in Women Previously Treated for an Adrenocortical Carcinoma
Pauline de Corbière, Katrin Ritzel, Laure Cazabat, et al.
Human Genetics
|
May 14, 2020
Genomic sequencing highlights the diverse molecular causes of Perrault syndrome: a peroxisomal disorder (PEX6), metabolic disorders (CLPP, GGPS1), and mtDNA maintenance/translation disorders (LARS2, TFAM)
Elena J Tucker, Rocio Rius, Sylvie Jaillard, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists
|
July 4, 2026
Early Metabolic Risk in Childhood Brain Cancer Survivors with Childhood-Onset Growth Hormone Deficiency
Alice Casiraghi, Olivier Pollé, Clément Bailly, et al.
The Journal of Clinical Endocrinology and Metabolism
|
August 1, 2014
The prevalence of CHD7 missense versus truncating mutations is higher in patients with Kallmann syndrome than in typical CHARGE patients
Séverine Marcos, Julie Sarfati, Chrystel Leroy, et al.
The Journal of Clinical Endocrinology and Metabolism
|
August 31, 2016
Gain-of-function Prolactin Receptor Variants Are Not Associated With Breast Cancer and Multiple Fibroadenoma Risk
Zeina Chakhtoura, Fatima Laki, Marie Bernadet, et al.
Annales D'Endocrinologie
|
March 7, 2024
Position statement on the diagnosis and management of congenital pituitary deficiency in adults: The French National Diagnosis and Treatment Protocol (NDTP)
Sarah Castets, Frédérique Albarel, Anne Bachelot, et al.
European Journal of Endocrinology
|
February 18, 2026
European Society for Paediatric Endocrinology (ESPE) and European Society of Endocrinology (ESE) joint clinical practice guidance for healthcare transition from paediatric to adult endocrine care
Enora Le Roux, Kirstine Stochholm, Martin Fassnacht, et al.
Hormone Research in Paediatrics
|
February 19, 2026
European Society for Paediatric Endocrinology and European Society of Endocrinology Joint Clinical Practice Guidance for Healthcare Transition from Paediatric to Adult Endocrine Care
Enora Le Roux, Kirstine Stochholm, Martin Fassnacht, et al.
Endocrine Reviews
|
May 7, 2021
Congenital Adrenal Hyperplasia-Current Insights in Pathophysiology, Diagnostics, and Management
Hedi L Claahsen-van der Grinten, Phyllis W Speiser, S Faisal Ahmed, et al.
Page
of 16