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Orphanet Journal of Rare Diseases|December 20, 2018
Evaluation of DSD training schools organized by cost action BM1303 "DSDnet"R Bertalan, A Lucas-Herald, Z Kolesinska, et al.Human Reproduction (Oxford, England)|August 6, 2010
Array-CGH analysis in patients with syndromic and non-syndromic XY gonadal dysgenesis: evaluation of array CGH as diagnostic tool and search for new candidate lociS Ledig, O Hiort, G Scherer, et al.Anatomy and Embryology|May 30, 1998
Immunohistochemistry and in situ hybridization of the androgen receptor in the developing human prostateG Aumüller, P M Holterhus, L Konrad, et al.Diabetic Medicine : a Journal of the British Diabetic Association|September 24, 2020
Parental expectations before and after 12-month experience with video consultations combined with regular outpatient care for children with type 1 diabetes: a qualitative studyS von Sengbusch, J Doerdelmann, S Lemke, et al.The Journal of Clinical Endocrinology and Metabolism|January 14, 2000
Basal inhibin B and the testosterone response to human chorionic gonadotropin correlate in prepubertal boysK Kubini, M Zachmann, N Albers, 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.Journal of Molecular Medicine (Berlin, Germany)|March 31, 2006
Tissue-specific transcription profiles of sex steroid biosynthesis enzymes and the androgen receptorU Hoppe, P-M Holterhus, L Wünsch, et al.European Journal of Pediatrics|September 15, 1999
Expression of two functionally different androgen receptors in a patient with androgen insensitivityP M Holterhus, G H Sinnecker, H A Wollmann, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|July 29, 2010
Psychosexual development in children with disorder of sex development (DSD)--results from the German Clinical Evaluation StudyM Jürgensen, E Kleinemeier, A Lux, et al.Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|August 7, 2009
Selective deficiency of Gsalpha and the possible role of alternative gene products of GNAS in Albright hereditary osteodystrophy and pseudohypoparathyroidism type IaS Thiele, R Werner, W Ahrens, et al.Pageof 9