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European Journal of Endocrinology
|
September 30, 2003
Effect of GH replacement therapy in two male siblings with combined X-linked hypophosphatemia and partial GH deficiency
Snjezana M Schütt, Marius Schumacher, Paul M Holterhus, et al.
Endocrine Connections
|
February 6, 2025
Satisfaction with health care among people with differences of sex development (DSD) in Germany
Maike Schnoor, Andreas Heidenreich, Martina Jürgensen, et al.
The Journal of Clinical Endocrinology and Metabolism
|
June 1, 2014
Different pattern of epigenetic changes of the GNAS gene locus in patients with pseudohypoparathyroidism type Ic confirm the heterogeneity of underlying pathomechanisms in this subgroup of pseudohypoparathyroidism and the demand for a new classification of GNAS-related disorders
Bettina Brix, Ralf Werner, Pia Staedt, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
February 3, 2016
Severe Undervirilisation in a 46,XY Case Due to a Novel Mutation in HSD17B3 Gene
Ayfer Alikaşifoğlu, Doğuş Vurallı, Olaf Hiort, et al.
Orphanet Journal of Rare Diseases
|
March 13, 2025
Correction to: Quality of care for people with differences of sex development (DSD) in Germany
Maike Schnoor, Andreas Heidenreich, Martina Jürgensen, et al.
The Journal of Steroid Biochemistry and Molecular Biology
|
February 6, 2021
In vitro functional characterization of androgen receptor gene mutations at arginine p.856 of the ligand-binding-domain associated with androgen insensitivity syndrome
Asma Tajouri, Maher Kharrat, Mediha Trabelsi, et al.
Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz
|
March 16, 2019
[The creation of a data protection policy: a guide to telemedicine healthcare projects]
Fabian-Simon Frielitz, Nicole Storm, Olaf Hiort, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
August 11, 2012
17beta-hydroxysteroid dehydrogenase type 3 deficiency as a result of a homozygous 7 base pair deletion in 17betaHSD3 gene
Ayfer Alikasifoglu, Olaf Hiort, Nazli Gonc, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
|
June 6, 2024
Is sex still binary?
Christoph Rehmann-Sutter, Olaf Hiort, Ulrike M Krämer, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG
|
January 14, 2009
First diagnosis of Martin-Albright syndrome in a 58-year-old patient
Sven R Quist, Ingolf Franke, Olaf Hiort, et al.
Page
of 20
Search research articles
Search
Showing results (51-60 of 195) with videos related to
Sort By:
Page
of 20
European Journal of Endocrinology
|
September 30, 2003
Effect of GH replacement therapy in two male siblings with combined X-linked hypophosphatemia and partial GH deficiency
Snjezana M Schütt, Marius Schumacher, Paul M Holterhus, et al.
Endocrine Connections
|
February 6, 2025
Satisfaction with health care among people with differences of sex development (DSD) in Germany
Maike Schnoor, Andreas Heidenreich, Martina Jürgensen, et al.
The Journal of Clinical Endocrinology and Metabolism
|
June 1, 2014
Different pattern of epigenetic changes of the GNAS gene locus in patients with pseudohypoparathyroidism type Ic confirm the heterogeneity of underlying pathomechanisms in this subgroup of pseudohypoparathyroidism and the demand for a new classification of GNAS-related disorders
Bettina Brix, Ralf Werner, Pia Staedt, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
February 3, 2016
Severe Undervirilisation in a 46,XY Case Due to a Novel Mutation in HSD17B3 Gene
Ayfer Alikaşifoğlu, Doğuş Vurallı, Olaf Hiort, et al.
Orphanet Journal of Rare Diseases
|
March 13, 2025
Correction to: Quality of care for people with differences of sex development (DSD) in Germany
Maike Schnoor, Andreas Heidenreich, Martina Jürgensen, et al.
The Journal of Steroid Biochemistry and Molecular Biology
|
February 6, 2021
In vitro functional characterization of androgen receptor gene mutations at arginine p.856 of the ligand-binding-domain associated with androgen insensitivity syndrome
Asma Tajouri, Maher Kharrat, Mediha Trabelsi, et al.
Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz
|
March 16, 2019
[The creation of a data protection policy: a guide to telemedicine healthcare projects]
Fabian-Simon Frielitz, Nicole Storm, Olaf Hiort, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
August 11, 2012
17beta-hydroxysteroid dehydrogenase type 3 deficiency as a result of a homozygous 7 base pair deletion in 17betaHSD3 gene
Ayfer Alikasifoglu, Olaf Hiort, Nazli Gonc, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
|
June 6, 2024
Is sex still binary?
Christoph Rehmann-Sutter, Olaf Hiort, Ulrike M Krämer, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG
|
January 14, 2009
First diagnosis of Martin-Albright syndrome in a 58-year-old patient
Sven R Quist, Ingolf Franke, Olaf Hiort, et al.
Page
of 20