Hiort O - Search Results

1

Luczay A, Sólyom J, Hiort O, Szabó E, Dobos M, Jenovári Z, Fekete G. Luczay A, et al. Among authors: hiort o. Orv Hetil. 2006 Sep 17;147(37):1805-7. Orv Hetil. 2006. PMID: 17131800 Hungarian.

2

The molecular basis of androgen insensitivity.

Nitsche EM, Hiort O. Nitsche EM, et al. Among authors: hiort o. Horm Res. 2000;54(5-6):327-33. doi: 10.1159/000053282. Horm Res. 2000. PMID: 11595828 Review.

3

Mutational analysis of Hungarian patients with androgen insensitivity syndrome.

Scheiber D, Barta C, Halász Z, Sallai A, Rácz K, Ságodi L, Fekete G, Hiort O, Sólyom J. Scheiber D, et al. Among authors: hiort o. J Pediatr Endocrinol Metab. 2003 Mar;16(3):367-73. doi: 10.1515/jpem.2003.16.3.367. J Pediatr Endocrinol Metab. 2003. PMID: 12705360

4

Single strand conformation polymorphism analysis of androgen receptor gene mutations in patients with androgen insensitivity syndromes: application for diagnosis, genetic counseling, and therapy.

Hiort O, Huang Q, Sinnecker GH, Sadeghi-Nejad A, Kruse K, Wolfe HJ, Yandell DW. Hiort O, et al. J Clin Endocrinol Metab. 1993 Jul;77(1):262-6. doi: 10.1210/jcem.77.1.8325950. J Clin Endocrinol Metab. 1993. PMID: 8325950

5

The clinical and molecular spectrum of androgen insensitivity syndromes.

Hiort O, Sinnecker GH, Holterhus PM, Nitsche EM, Kruse K. Hiort O, et al. Am J Med Genet. 1996 May 3;63(1):218-22. doi: 10.1002/(SICI)1096-8628(19960503)63:1<218::AID-AJMG38>3.0.CO;2-P. Am J Med Genet. 1996. PMID: 8723113

6

Mosaicism due to a somatic mutation of the androgen receptor gene determines phenotype in androgen insensitivity syndrome.

Holterhus PM, Brüggenwirth HT, Hiort O, Kleinkauf-Houcken A, Kruse K, Sinnecker GH, Brinkmann AO. Holterhus PM, et al. Among authors: hiort o. J Clin Endocrinol Metab. 1997 Nov;82(11):3584-9. doi: 10.1210/jcem.82.11.4375. J Clin Endocrinol Metab. 1997. PMID: 9360511

7

Expression of two functionally different androgen receptors in a patient with androgen insensitivity.

Holterhus PM, Sinnecker GH, Wollmann HA, Struve D, Homburg N, Kruse K, Hiort O. Holterhus PM, et al. Among authors: hiort o. Eur J Pediatr. 1999 Sep;158(9):702-6. doi: 10.1007/s004310051183. Eur J Pediatr. 1999. PMID: 10485299

8

Clinical and molecular spectrum of somatic mosaicism in androgen insensitivity syndrome.

Holterhus PM, Wiebel J, Sinnecker GH, Brüggenwirth HT, Sippell WG, Brinkmann AO, Kruse K, Hiort O. Holterhus PM, et al. Among authors: hiort o. Pediatr Res. 1999 Dec;46(6):684-90. doi: 10.1203/00006450-199912000-00009. Pediatr Res. 1999. PMID: 10590024

9

Phenotypic diversity and testosterone-induced normalization of mutant L712F androgen receptor function in a kindred with androgen insensitivity.

Holterhus PM, Sinnecker GH, Hiort O. Holterhus PM, et al. Among authors: hiort o. J Clin Endocrinol Metab. 2000 Sep;85(9):3245-50. doi: 10.1210/jcem.85.9.6812. J Clin Endocrinol Metab. 2000. PMID: 10999816 Clinical Trial.

10

Transcription of androgen receptor and 5alpha-reductase II in genital fibroblasts from patients with androgen insensitivity syndrome.

Hellwinkel OJ, Bassler J, Hiort O. Hellwinkel OJ, et al. Among authors: hiort o. J Steroid Biochem Mol Biol. 2000 Dec 31;75(4-5):213-8. doi: 10.1016/s0960-0760(00)00174-6. J Steroid Biochem Mol Biol. 2000. PMID: 11282274

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