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International Journal of Endocrinology
|
August 14, 2012
Disorders of sex development and hypogonadism: genetics, mechanism, and therapies
Gil Guerra-Junior, Ana Claudia Latronico, Olaf Hiort, et al.
European Journal of Endocrinology
|
October 27, 2020
Validation of a next-generation sequencing (NGS) panel to improve the diagnosis of X-linked hypophosphataemia (XLH) and other genetic disorders of renal phosphate wasting
Susanne Thiele, Ralf Werner, Annika Stubbe, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
August 10, 2011
A new heterozygous mutation (D196N) in the Gs alpha gene as a cause for pseudohypoparathyroidism type IA in a boy who had gallstones
Julia Winter, Olaf Hiort, Pia Hermanns, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
April 26, 2003
A novel point mutation in the hormone binding domain of the androgen receptor associated with partial and minimal androgen insensitivity syndrome
Assimina Galli-Tsinopoulou, Olaf Hiort, Tobias Schuster, et al.
Endocrine Connections
|
February 17, 2022
ENDO-ERN ON RARE ENDOCRINE CONDITIONS: Endo-ERN in its fifth year: a pinch of care, science, curiosity and new horizons
Violeta Iotova, Jerome Bertherat, George Mastorakos, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology
|
October 31, 2006
17beta-hydroxysteroid dehydrogenase-3 deficiency: a rare endocrine cause of male-to-female sex reversal
Silvano Bertelloni, M Cristina Maggio, Giovanni Federico, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
|
June 6, 2024
The Role of Genetics in Sex Diversity
Olaf Hiort, Ulrike Krämer, Lisa Malich, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
August 4, 2011
Hereditary vitamin D-resistant rickets (HVDRR) owing to a heterozygous mutation in the vitamin D receptor
Peter J Malloy, Yulin Zhou, Jining Wang, et al.
Treatments in Endocrinology
|
January 15, 2005
Deciding on gender in children with intersex conditions: considerations and controversies
Ute Thyen, Hertha Richter-Appelt, Claudia Wiesemann, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 18, 2011
Satisfaction with genital surgery and sexual life of adults with XY disorders of sex development: results from the German clinical evaluation study
Birgit Köhler, Eva Kleinemeier, Anke Lux, et al.
Page
of 20
Search research articles
Search
Showing results (41-50 of 195) with videos related to
Sort By:
Page
of 20
International Journal of Endocrinology
|
August 14, 2012
Disorders of sex development and hypogonadism: genetics, mechanism, and therapies
Gil Guerra-Junior, Ana Claudia Latronico, Olaf Hiort, et al.
European Journal of Endocrinology
|
October 27, 2020
Validation of a next-generation sequencing (NGS) panel to improve the diagnosis of X-linked hypophosphataemia (XLH) and other genetic disorders of renal phosphate wasting
Susanne Thiele, Ralf Werner, Annika Stubbe, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
August 10, 2011
A new heterozygous mutation (D196N) in the Gs alpha gene as a cause for pseudohypoparathyroidism type IA in a boy who had gallstones
Julia Winter, Olaf Hiort, Pia Hermanns, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
April 26, 2003
A novel point mutation in the hormone binding domain of the androgen receptor associated with partial and minimal androgen insensitivity syndrome
Assimina Galli-Tsinopoulou, Olaf Hiort, Tobias Schuster, et al.
Endocrine Connections
|
February 17, 2022
ENDO-ERN ON RARE ENDOCRINE CONDITIONS: Endo-ERN in its fifth year: a pinch of care, science, curiosity and new horizons
Violeta Iotova, Jerome Bertherat, George Mastorakos, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology
|
October 31, 2006
17beta-hydroxysteroid dehydrogenase-3 deficiency: a rare endocrine cause of male-to-female sex reversal
Silvano Bertelloni, M Cristina Maggio, Giovanni Federico, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
|
June 6, 2024
The Role of Genetics in Sex Diversity
Olaf Hiort, Ulrike Krämer, Lisa Malich, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
August 4, 2011
Hereditary vitamin D-resistant rickets (HVDRR) owing to a heterozygous mutation in the vitamin D receptor
Peter J Malloy, Yulin Zhou, Jining Wang, et al.
Treatments in Endocrinology
|
January 15, 2005
Deciding on gender in children with intersex conditions: considerations and controversies
Ute Thyen, Hertha Richter-Appelt, Claudia Wiesemann, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 18, 2011
Satisfaction with genital surgery and sexual life of adults with XY disorders of sex development: results from the German clinical evaluation study
Birgit Köhler, Eva Kleinemeier, Anke Lux, et al.
Page
of 20