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International Journal of Environmental Research and Public Health
|
August 8, 2018
Recommendations for Improving the Quality of Rare Disease Registries
Yllka Kodra, Jérôme Weinbach, Manuel Posada-de-la-Paz, et al.
Human Molecular Genetics
|
January 11, 2007
Functional characterization of GATA3 mutations causing the hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome: insight into mechanisms of DNA binding by the GATA3 transcription factor
Asif Ali, Paul T Christie, Irina V Grigorieva, et al.
Hormone Research in Paediatrics
|
October 19, 2018
Management of Gonads in Adults with Androgen Insensitivity: An International Survey
Lloyd J W Tack, Ellen Maris, Leendert H J Looijenga, et al.
Endocrine Connections
|
October 13, 2022
The genetic diagnosis of rare endocrine disorders of sex development and maturation: a survey among Endo-ERN centres
Luca Persani, Martine Cools, Stamatina Ioakim, et al.
European Journal of Endocrinology
|
March 15, 2022
Treatment of congenital adrenal hyperplasia in children aged 0-3 years: a retrospective multicenter analysis of salt supplementation, glucocorticoid and mineralocorticoid medication, growth and blood pressure
Uta Neumann, Annelieke van der Linde, Ruth E Krone, et al.
Clinical Endocrinology
|
July 22, 2025
Development of a Minimum Dataset for the Global Monitoring of the Safety and Efficacy of Growth Hormone Replacement in Adults With Growth Hormone Deficiency (AGHD)
Suet Ching Chen, Angela K Lucas-Herald, Ruoning Tang, et al.
European Journal of Endocrinology
|
May 19, 2026
Growth Patterns and Bone Maturation in Children with Sex Chromosomal (45,X/46,XY) DSD
Jessica Bosmans, Nele Herregods, Ineke van Gremberghe, et al.
European Journal of Endocrinology
|
October 14, 2023
Hormonal control during infancy and testicular adrenal rest tumor development in males with congenital adrenal hyperplasia: a retrospective multicenter cohort study
Mariska A M Schröder, Mihaela Neacşu, Bas P H Adriaansen, et al.
European Journal of Endocrinology
|
March 2, 2022
Prenatal dexamethasone treatment for classic 21-hydroxylase deficiency in Europe
Hanna Nowotny, Uta Neumann, Véronique Tardy-Guidollet, et al.
Nature Reviews. Endocrinology
|
July 1, 2018
Diagnosis and management of pseudohypoparathyroidism and related disorders: first international Consensus Statement
Giovanna Mantovani, Murat Bastepe, David Monk, et al.
Page
of 21
Search research articles
Search
Showing results (181-190 of 203) with videos related to
Sort By:
Page
of 21
International Journal of Environmental Research and Public Health
|
August 8, 2018
Recommendations for Improving the Quality of Rare Disease Registries
Yllka Kodra, Jérôme Weinbach, Manuel Posada-de-la-Paz, et al.
Human Molecular Genetics
|
January 11, 2007
Functional characterization of GATA3 mutations causing the hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome: insight into mechanisms of DNA binding by the GATA3 transcription factor
Asif Ali, Paul T Christie, Irina V Grigorieva, et al.
Hormone Research in Paediatrics
|
October 19, 2018
Management of Gonads in Adults with Androgen Insensitivity: An International Survey
Lloyd J W Tack, Ellen Maris, Leendert H J Looijenga, et al.
Endocrine Connections
|
October 13, 2022
The genetic diagnosis of rare endocrine disorders of sex development and maturation: a survey among Endo-ERN centres
Luca Persani, Martine Cools, Stamatina Ioakim, et al.
European Journal of Endocrinology
|
March 15, 2022
Treatment of congenital adrenal hyperplasia in children aged 0-3 years: a retrospective multicenter analysis of salt supplementation, glucocorticoid and mineralocorticoid medication, growth and blood pressure
Uta Neumann, Annelieke van der Linde, Ruth E Krone, et al.
Clinical Endocrinology
|
July 22, 2025
Development of a Minimum Dataset for the Global Monitoring of the Safety and Efficacy of Growth Hormone Replacement in Adults With Growth Hormone Deficiency (AGHD)
Suet Ching Chen, Angela K Lucas-Herald, Ruoning Tang, et al.
European Journal of Endocrinology
|
May 19, 2026
Growth Patterns and Bone Maturation in Children with Sex Chromosomal (45,X/46,XY) DSD
Jessica Bosmans, Nele Herregods, Ineke van Gremberghe, et al.
European Journal of Endocrinology
|
October 14, 2023
Hormonal control during infancy and testicular adrenal rest tumor development in males with congenital adrenal hyperplasia: a retrospective multicenter cohort study
Mariska A M Schröder, Mihaela Neacşu, Bas P H Adriaansen, et al.
European Journal of Endocrinology
|
March 2, 2022
Prenatal dexamethasone treatment for classic 21-hydroxylase deficiency in Europe
Hanna Nowotny, Uta Neumann, Véronique Tardy-Guidollet, et al.
Nature Reviews. Endocrinology
|
July 1, 2018
Diagnosis and management of pseudohypoparathyroidism and related disorders: first international Consensus Statement
Giovanna Mantovani, Murat Bastepe, David Monk, et al.
Page
of 21