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Urology
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August 16, 2005
A novel missense mutation of 5-alpha reductase type 2 gene (SRD5A2) leads to severe male pseudohermaphroditism in a Turkish family
Mithat 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 deficiency
Susanne 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 mutation
Serap 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 deficiency
Olaf 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 constructs
Ralf 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 therapy
Paul-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 signalling
Mostafa 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 interaction
Felix G Riepe, Olaf Hiort, Joachim Grötzinger, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
May 6, 2003
Puberty in disorders of somatosexual differentiation
Olaf Hiort, Sandra Reinecke, Ute Thyen, et al.
Page
of 20
Search research articles
Search
Showing results (71-80 of 195) with videos related to
Sort By:
Page
of 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 family
Mithat 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 deficiency
Susanne 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 mutation
Serap 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 deficiency
Olaf 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 constructs
Ralf 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 therapy
Paul-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 signalling
Mostafa 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 interaction
Felix G Riepe, Olaf Hiort, Joachim Grötzinger, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
May 6, 2003
Puberty in disorders of somatosexual differentiation
Olaf Hiort, Sandra Reinecke, Ute Thyen, et al.
Page
of 20