Olaf Hiort
Olaf Hiort
University of Luebeck
Verified email at uksh.de - Homepage
Cited by
Cited by
Consensus statement on management of intersex disorders
PA Lee, CP Houk, SF Ahmed, IA Hughes
Pediatrics 118 (2), e488-e500, 2006
Epidemiology and initial management of ambiguous genitalia at birth in Germany
U Thyen, K Lanz, PM Holterhus, O Hiort
Hormone research in paediatrics 66 (4), 195-203, 2006
Phenotypic classification of male pseudohermaphroditism due to steroid 5α‐reductase 2 deficiency
GHG Sinnecker, O Hiort, L Dibbelt, N Albers, HG Dörr, H Hauß, U Heinrich, ...
American journal of medical genetics 63 (1), 223-230, 1996
Significance of mutations in the androgen receptor gene in males with idiopathic infertility
O Hiort, PM Holterhus, T Horter, W Schulze, B Kremke, M Bals-Pratsch, ...
The Journal of Clinical Endocrinology & Metabolism 85 (8), 2810-2815, 2000
Summary of consensus statement on intersex disorders and their management
CP Houk, IA Hughes, SF Ahmed, PA Lee
Pediatrics 118 (2), 753-757, 2006
Analysis of RET protooncogene point mutations distinguishes heritable from nonheritable medullary thyroid carcinomas
EK Kunz, X Matias‐Guiu, O Hiort, G Christiansen, A Colomer, J Roth, ...
Cancer 76 (3), 479-489, 1995
A novel ultrapressure liquid chromatography tandem mass spectrometry method for the simultaneous determination of androstenedione, testosterone, and dihydrotestosterone in …
AE Kulle, FG Riepe, D Melchior, O Hiort, PM Holterhus
The Journal of Clinical Endocrinology & Metabolism 95 (5), 2399-2409, 2010
Epigenetic Defects of GNAS in Patients with Pseudohypoparathyroidism and Mild Features of Albright’s Hereditary Osteodystrophy
GP de Nanclares, E Fernández-Rebollo, I Santin, B Garcia-Cuartero, ...
The Journal of Clinical Endocrinology & Metabolism 92 (6), 2370-2373, 2007
Functional assessment and clinical classification of androgen sensitivity in patients with mutations of the androgen receptor gene
GHG Sinnecker, O Hiort, EM Nitsche, PM Holterhus, K Kruse, ...
European journal of pediatrics 156 (1), 7-14, 1996
The molecular basis of male sexual differentiation
O Hiort, H Paul-Martin
European journal of endocrinology 142 (2), 101-110, 2000
Basal inhibin B and the testosterone response to human chorionic gonadotropin correlate in prepubertal boys
K Kubini, M Zachmann, N Albers, O Hiort, M Bettendorf, J Wölfle, ...
The Journal of Clinical Endocrinology & Metabolism 85 (1), 134-138, 2000
Satisfaction with genital surgery and sexual life of adults with XY disorders of sex development: results from the German clinical evaluation study
B Köhler, E Kleinemeier, A Lux, O Hiort, A Grüters, U Thyen, ...
The Journal of Clinical Endocrinology & Metabolism 97 (2), 577-588, 2012
The clinical and molecular spectrum of androgen insensitivity syndromes
O Hiort, GHG Sinnecker, PM Holterhus, EM Nitsche, K Kruse
American journal of medical genetics 63 (1), 218-222, 1996
Etiologic classification of severe hypospadias: implications for prognosis and management
N Albert, C Ulrichs, S Glüer, O Hiort, GHG Sinnecker, H Mildenberger, ...
The Journal of pediatrics 131 (3), 386-392, 1997
Gender role behavior in children with XY karyotype and disorders of sex development
M Jürgensen, O Hiort, PM Holterhus, U Thyen
Hormones and behavior 51 (3), 443-453, 2007
Clinical, biochemical, and genetic findings in a large pedigree of male and female patients with 5 alpha-reductase 2 deficiency
Z Hochberg, R Chayen, N Reiss, Z Falik, A Makler, M Munichor, A Farkas, ...
The Journal of Clinical Endocrinology & Metabolism 81 (8), 2821-2827, 1996
Deletion and point mutations of PTHLH cause brachydactyly type E
E Klopocki, BP Hennig, K Dathe, R Koll, T de Ravel, E Baten, E Blom, ...
The American Journal of Human Genetics 86 (3), 434-439, 2010
The spectrum of phenotypes associated with mutations in steroidogenic factor 1 (SF-1, NR5A1, Ad4BP) includes severe penoscrotal hypospadias in 46, XY males without adrenal …
B Köhler, L Lin, I Mazen, C Cetindag, H Biebermann, I Akkurt, R Rossi, ...
European Journal of Endocrinology 161 (2), 237, 2009
Analysis of the GNAS1 gene in Albright’s hereditary osteodystrophy
W Ahrens, O Hiort, P Staedt, T Kirschner, C Marschke, K Kruse
The Journal of Clinical Endocrinology & Metabolism 86 (10), 4630-4634, 2001
Inherited and de novo androgen receptor gene mutations: investigation of single-case families
O Hiort, GHG Sinnecker, PM Holterhus, EM Nitsche, K Kruse
The Journal of pediatrics 132 (6), 939-943, 1998
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