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A Richter-Unruh

Showing results (1-10 of 14) with videos related to

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Urologie (Heidelberg, Germany)|April 4, 2024
[Differences in sexual development-S2k guideline update]S Krege, F Eckoldt, A Richter-Unruh, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|August 25, 2020
Establishment of Clinical and Lab Algorithms for the Identification of Carriers of Mutations in CYP21A2 - A Study of 365 Children and AdolescentsJ Meinel, T Haverkamp, F Wünsche, et al.
Hormone Research|January 30, 2002
Clinical and novel molecular findings in a 6.8-year-old Turkish boy with triple A syndromeK Schmittmann-Ohters, A Huebner, A Richter-Unruh, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|March 12, 2009
Mutation analysis of FOXF2 in patients with disorders of sex development (DSD) in combination with cleft palateU Jochumsen, R Werner, N Miura, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|April 9, 2008
Altered transcription profiles of key-enzymes of androgen biosynthesis in genital skin fibroblasts from patients with 46,XY disorders of sex development (DSD)U Hoppe, L Wünsch, P-M Holterhus, et al.
European Journal of Endocrinology|March 5, 2005
Novel insertion frameshift mutation of the LH receptor gene: problematic clinical distinction of Leydig cell hypoplasia from enzyme defects primarily affecting testosterone biosynthesisA Richter-Unruh, E Korsch, O Hiort, et al.
The Journal of Clinical Endocrinology and Metabolism|October 9, 2004
Leydig cell hypoplasia: absent luteinizing hormone receptor cell surface expression caused by a novel homozygous mutation in the extracellular domainA Richter-Unruh, M Verhoef-Post, S Malak, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|March 25, 2005
Clinical characteristics of type 2 diabetes mellitus in overweight European caucasian adolescentsT Reinehr, W Andler, T Kapellen, et al.
The Journal of Clinical Endocrinology and Metabolism|March 13, 2002
Male LH-independent sexual precocity in a 3.5-year-old boy caused by a somatic activating mutation of the LH receptor in a Leydig cell tumorA Richter-Unruh, H T Wessels, U Menken, et al.
The Journal of Clinical Endocrinology and Metabolism|June 7, 2002
Mutant luteinizing hormone receptors in a compound heterozygous patient with complete Leydig cell hypoplasia: abnormal processing causes signaling deficiencyJ W M Martens, S Lumbroso, M Verhoef-Post, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Urologie (Heidelberg, Germany)|April 4, 2024
[Differences in sexual development-S2k guideline update]S Krege, F Eckoldt, A Richter-Unruh, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|August 25, 2020
Establishment of Clinical and Lab Algorithms for the Identification of Carriers of Mutations in CYP21A2 - A Study of 365 Children and AdolescentsJ Meinel, T Haverkamp, F Wünsche, et al.
Hormone Research|January 30, 2002
Clinical and novel molecular findings in a 6.8-year-old Turkish boy with triple A syndromeK Schmittmann-Ohters, A Huebner, A Richter-Unruh, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|March 12, 2009
Mutation analysis of FOXF2 in patients with disorders of sex development (DSD) in combination with cleft palateU Jochumsen, R Werner, N Miura, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|April 9, 2008
Altered transcription profiles of key-enzymes of androgen biosynthesis in genital skin fibroblasts from patients with 46,XY disorders of sex development (DSD)U Hoppe, L Wünsch, P-M Holterhus, et al.
European Journal of Endocrinology|March 5, 2005
Novel insertion frameshift mutation of the LH receptor gene: problematic clinical distinction of Leydig cell hypoplasia from enzyme defects primarily affecting testosterone biosynthesisA Richter-Unruh, E Korsch, O Hiort, et al.
The Journal of Clinical Endocrinology and Metabolism|October 9, 2004
Leydig cell hypoplasia: absent luteinizing hormone receptor cell surface expression caused by a novel homozygous mutation in the extracellular domainA Richter-Unruh, M Verhoef-Post, S Malak, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|March 25, 2005
Clinical characteristics of type 2 diabetes mellitus in overweight European caucasian adolescentsT Reinehr, W Andler, T Kapellen, et al.
The Journal of Clinical Endocrinology and Metabolism|March 13, 2002
Male LH-independent sexual precocity in a 3.5-year-old boy caused by a somatic activating mutation of the LH receptor in a Leydig cell tumorA Richter-Unruh, H T Wessels, U Menken, et al.
The Journal of Clinical Endocrinology and Metabolism|June 7, 2002
Mutant luteinizing hormone receptors in a compound heterozygous patient with complete Leydig cell hypoplasia: abnormal processing causes signaling deficiencyJ W M Martens, S Lumbroso, M Verhoef-Post, et al.
Pageof 2