Hiort O - Search Results

1

Oestrogen versus androgen in hormone-replacement therapy for complete androgen insensitivity syndrome: a multicentre, randomised, double-dummy, double-blind crossover trial.

Birnbaum W, Marshall L, Werner R, Kulle A, Holterhus PM, Rall K, Köhler B, Richter-Unruh A, Hartmann MF, Wudy SA, Auer MK, Lux A, Kropf S, Hiort O. Birnbaum W, et al. Among authors: hiort o. Lancet Diabetes Endocrinol. 2018 Oct;6(10):771-780. doi: 10.1016/S2213-8587(18)30197-9. Epub 2018 Jul 31. Lancet Diabetes Endocrinol. 2018. PMID: 30075954 Clinical Trial.

2

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

3

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

4

Functional assessment and clinical classification of androgen sensitivity in patients with mutations of the androgen receptor gene. German Collaborative Intersex Study Group.

Sinnecker GH, Hiort O, Nitsche EM, Holterhus PM, Kruse K. Sinnecker GH, et al. Among authors: hiort o. Eur J Pediatr. 1997 Jan;156(1):7-14. doi: 10.1007/s004310050542. Eur J Pediatr. 1997. PMID: 9007482

5

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

6

Inherited and de novo androgen receptor gene mutations: investigation of single-case families.

Hiort O, Sinnecker GH, Holterhus PM, Nitsche EM, Kruse K. Hiort O, et al. J Pediatr. 1998 Jun;132(6):939-43. doi: 10.1016/s0022-3476(98)70387-7. J Pediatr. 1998. PMID: 9627582

7

Physiology and pathophysiology of androgen action.

Hiort O, Holterhus PM, Nitsche EM. Hiort O, et al. Baillieres Clin Endocrinol Metab. 1998 Apr;12(1):115-32. doi: 10.1016/s0950-351x(98)80495-3. Baillieres Clin Endocrinol Metab. 1998. PMID: 9890064 Review.

8

Complete androgen insensitivity caused by a splice donor site mutation in intron 2 of the human androgen receptor gene resulting in an exon 2-lacking transcript with premature stop-codon and reduced expression.

Hellwinkel OJ, Bull K, Holterhus PM, Homburg N, Struve D, Hiort O. Hellwinkel OJ, et al. Among authors: hiort o. J Steroid Biochem Mol Biol. 1999 Jan;68(1-2):1-9. doi: 10.1016/s0960-0760(98)00157-5. J Steroid Biochem Mol Biol. 1999. PMID: 10215032

9

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

10

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

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