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Olaf Hiort

Showing results (51-60 of 195) with videos related to

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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 deficiencySnjezana 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 GermanyMaike 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 disordersBettina 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 GeneAyfer 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 GermanyMaike 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 syndromeAsma 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 geneAyfer 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 patientSven R Quist, Ingolf Franke, Olaf Hiort, et al.
Pageof 20

Showing results (51-60 of 195) with videos related to

Sort By:
Pageof 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 deficiencySnjezana 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 GermanyMaike 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 disordersBettina 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 GeneAyfer 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 GermanyMaike 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 syndromeAsma 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 geneAyfer 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 patientSven R Quist, Ingolf Franke, Olaf Hiort, et al.
Pageof 20