Search research articles
Contact Us
Filters
Showing results (171-180 of 195) with videos related to
Page
of 20
Sort By:
The Journal of Clinical Endocrinology and Metabolism
|
July 6, 2019
Response to Letter to the Editor: "Clinical but Not Histological Outcomes in Males With 45,X/46,XY Mosaicism Vary Depending on Reason for Diagnosis"
Marie Lindhardt Ljubicic, Anne Jørgensen, Juliana Gabriel Ribeiro de Andrade, et al.
European Journal of Endocrinology
|
January 9, 2025
Gonadal function and pathology in 17beta-HSD 3 and 5alpha-reductase deficiency
Lidewij S Boogers, Hennie T Brüggenwirth, Katja P Wolffenbuttel, et al.
BMC Endocrine Disorders
|
June 27, 2022
Development and evaluation of a patient education programme for children, adolescents, and young adults with differences of sex development (DSD) and their parents: study protocol of Empower-DSD
Sabine Wiegmann, Martina Ernst, Loretta Ihme, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 25, 2023
Effects of Burosumab Treatment on Mineral Metabolism in Children and Adolescents With X-linked Hypophosphatemia
Annika Ewert, Mirko Rehberg, Karl Peter Schlingmann, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 9, 2012
PRKAR1A and PDE4D mutations cause acrodysostosis but two distinct syndromes with or without GPCR-signaling hormone resistance
Agnès Linglart, Helena Fryssira, Olaf Hiort, et al.
Geburtshilfe Und Frauenheilkunde
|
December 13, 2021
Diagnosis and Therapy of Female Genital Malformations (Part 1). Guideline of the DGGG, OEGGG and SGGG (S2k Level, AWMF Registry Number 015/052, May 2019)
Peter Oppelt, Helge Binder, Jacques Birraux, et al.
Geburtshilfe Und Frauenheilkunde
|
December 13, 2021
Diagnosis and Therapy of Female Genital Malformations (Part 2). Guideline of the DGGG, OEGGG and SGGG (S2k Level, AWMF Registry Number 015/052, May 2019)
Peter Oppelt, Helge Binder, Jacques Birraux, et al.
Calcified Tissue International
|
March 28, 2025
Office Blood Pressure and Obesity in Children with X-Linked Hypophosphatemia
Ineke Böckmann, Maren Leifheit-Nestler, Mirko Rehberg, et al.
Journal of Medical Genetics
|
January 22, 2015
Copy number variation of two separate regulatory regions upstream of SOX9 causes isolated 46,XY or 46,XX disorder of sex development
Gwang-Jin Kim, Elisabeth Sock, Astrid Buchberger, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 3, 2025
Gonadal Function And Its Evolution In 46, XX Testicular/Ovotesticular DSD
Margherita Sepich, Silvano Bertelloni, Nina Tyutyusheva, et al.
Page
of 20
Search research articles
Search
Showing results (171-180 of 195) with videos related to
Sort By:
Page
of 20
The Journal of Clinical Endocrinology and Metabolism
|
July 6, 2019
Response to Letter to the Editor: "Clinical but Not Histological Outcomes in Males With 45,X/46,XY Mosaicism Vary Depending on Reason for Diagnosis"
Marie Lindhardt Ljubicic, Anne Jørgensen, Juliana Gabriel Ribeiro de Andrade, et al.
European Journal of Endocrinology
|
January 9, 2025
Gonadal function and pathology in 17beta-HSD 3 and 5alpha-reductase deficiency
Lidewij S Boogers, Hennie T Brüggenwirth, Katja P Wolffenbuttel, et al.
BMC Endocrine Disorders
|
June 27, 2022
Development and evaluation of a patient education programme for children, adolescents, and young adults with differences of sex development (DSD) and their parents: study protocol of Empower-DSD
Sabine Wiegmann, Martina Ernst, Loretta Ihme, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 25, 2023
Effects of Burosumab Treatment on Mineral Metabolism in Children and Adolescents With X-linked Hypophosphatemia
Annika Ewert, Mirko Rehberg, Karl Peter Schlingmann, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 9, 2012
PRKAR1A and PDE4D mutations cause acrodysostosis but two distinct syndromes with or without GPCR-signaling hormone resistance
Agnès Linglart, Helena Fryssira, Olaf Hiort, et al.
Geburtshilfe Und Frauenheilkunde
|
December 13, 2021
Diagnosis and Therapy of Female Genital Malformations (Part 1). Guideline of the DGGG, OEGGG and SGGG (S2k Level, AWMF Registry Number 015/052, May 2019)
Peter Oppelt, Helge Binder, Jacques Birraux, et al.
Geburtshilfe Und Frauenheilkunde
|
December 13, 2021
Diagnosis and Therapy of Female Genital Malformations (Part 2). Guideline of the DGGG, OEGGG and SGGG (S2k Level, AWMF Registry Number 015/052, May 2019)
Peter Oppelt, Helge Binder, Jacques Birraux, et al.
Calcified Tissue International
|
March 28, 2025
Office Blood Pressure and Obesity in Children with X-Linked Hypophosphatemia
Ineke Böckmann, Maren Leifheit-Nestler, Mirko Rehberg, et al.
Journal of Medical Genetics
|
January 22, 2015
Copy number variation of two separate regulatory regions upstream of SOX9 causes isolated 46,XY or 46,XX disorder of sex development
Gwang-Jin Kim, Elisabeth Sock, Astrid Buchberger, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 3, 2025
Gonadal Function And Its Evolution In 46, XX Testicular/Ovotesticular DSD
Margherita Sepich, Silvano Bertelloni, Nina Tyutyusheva, et al.
Page
of 20