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Olaf Hiort

Showing results (71-80 of 195) with videos related to

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Urology|August 16, 2005
A novel missense mutation of 5-alpha reductase type 2 gene (SRD5A2) leads to severe male pseudohermaphroditism in a Turkish familyMithat Bahceci, Ahmet Resit Ersay, Alpaslan Tuzcu, et al.
The Journal of Clinical Endocrinology and Metabolism|February 15, 2007
A disruptive mutation in exon 3 of the GNAS gene with albright hereditary osteodystrophy, normocalcemic pseudohypoparathyroidism, and selective long transcript variant Gsalpha-L deficiencySusanne Thiele, Ralf Werner, Wiebke Ahrens, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 20, 2009
Pseudohypoparathyroidism type IA (PHP-Ia): maternally inherited GNAS gene mutationSerap Semiz, Fusun Duzcan, Masallah Candemir, et al.
International Journal of Andrology|March 1, 2002
A novel homozygous disruptive mutation in the SRD5A2-gene in a partially virilized patient with 5alpha-reductase deficiencyOlaf Hiort, Snjezana M Schütt, Monika Bals-Pratsch, et al.
The Journal of Steroid Biochemistry and Molecular Biology|August 26, 2006
Androgen receptor gene mutations in androgen insensitivity syndrome cause distinct patterns of reduced activation of androgen-responsive promoter constructsRalf Werner, Jenny Schütt, Sabine Hannema, et al.
Diabetes Care|March 1, 2007
Classification of distinct baseline insulin infusion patterns in children and adolescents with type 1 diabetes on continuous subcutaneous insulin infusion therapyPaul-Martin Holterhus, Rainer Odendahl, Sandra Oesingmann, et al.
European Journal of Endocrinology|February 1, 2023
Persistence of foetal testicular features in patients with defective androgen signallingMostafa Al-Sharkawi, Verónica Calonga-Solís, Franz F Dressler, et al.
Hormone Research in Paediatrics|December 13, 2016
Pubertal Development in
17Beta-Hydroxysteroid Dehydrogenase Type 3 Deficiency
Olaf Hiort, Louise Marshall, Wiebke Birnbaum, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 2008
Functional and structural consequences of a novel point mutation in the CYP21A2 gene causing congenital adrenal hyperplasia: potential relevance of helix C for P450 oxidoreductase-21-hydroxylase interactionFelix G Riepe, Olaf Hiort, Joachim Grötzinger, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 6, 2003
Puberty in disorders of somatosexual differentiationOlaf Hiort, Sandra Reinecke, Ute Thyen, et al.
Pageof 20

Showing results (71-80 of 195) with videos related to

Sort By:
Pageof 20
Urology|August 16, 2005
A novel missense mutation of 5-alpha reductase type 2 gene (SRD5A2) leads to severe male pseudohermaphroditism in a Turkish familyMithat Bahceci, Ahmet Resit Ersay, Alpaslan Tuzcu, et al.
The Journal of Clinical Endocrinology and Metabolism|February 15, 2007
A disruptive mutation in exon 3 of the GNAS gene with albright hereditary osteodystrophy, normocalcemic pseudohypoparathyroidism, and selective long transcript variant Gsalpha-L deficiencySusanne Thiele, Ralf Werner, Wiebke Ahrens, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 20, 2009
Pseudohypoparathyroidism type IA (PHP-Ia): maternally inherited GNAS gene mutationSerap Semiz, Fusun Duzcan, Masallah Candemir, et al.
International Journal of Andrology|March 1, 2002
A novel homozygous disruptive mutation in the SRD5A2-gene in a partially virilized patient with 5alpha-reductase deficiencyOlaf Hiort, Snjezana M Schütt, Monika Bals-Pratsch, et al.
The Journal of Steroid Biochemistry and Molecular Biology|August 26, 2006
Androgen receptor gene mutations in androgen insensitivity syndrome cause distinct patterns of reduced activation of androgen-responsive promoter constructsRalf Werner, Jenny Schütt, Sabine Hannema, et al.
Diabetes Care|March 1, 2007
Classification of distinct baseline insulin infusion patterns in children and adolescents with type 1 diabetes on continuous subcutaneous insulin infusion therapyPaul-Martin Holterhus, Rainer Odendahl, Sandra Oesingmann, et al.
European Journal of Endocrinology|February 1, 2023
Persistence of foetal testicular features in patients with defective androgen signallingMostafa Al-Sharkawi, Verónica Calonga-Solís, Franz F Dressler, et al.
Hormone Research in Paediatrics|December 13, 2016
Pubertal Development in
17Beta-Hydroxysteroid Dehydrogenase Type 3 Deficiency
Olaf Hiort, Louise Marshall, Wiebke Birnbaum, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 2008
Functional and structural consequences of a novel point mutation in the CYP21A2 gene causing congenital adrenal hyperplasia: potential relevance of helix C for P450 oxidoreductase-21-hydroxylase interactionFelix G Riepe, Olaf Hiort, Joachim Grötzinger, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 6, 2003
Puberty in disorders of somatosexual differentiationOlaf Hiort, Sandra Reinecke, Ute Thyen, et al.
Pageof 20