Hiort O - Search Results

1

Response to Letter to the Editor: "Clinical but Not Histological Outcomes in Males With 45,X/46,XY Mosaicism Vary Depending on Reason for Diagnosis".

Ljubicic ML, Jørgensen A, Ribeiro de Andrade JG, Balsamo A, Bertelloni S, Cools M, Cuccaro RT, Darendeliler F, Flück CE, Grinspon RP, Maciel-Guerra A, Guran T, Hannema SE, Lucas-Herald AK, Hiort O, Holterhus PM, Lichiardopol C, Looijenga LHJ, Ortolano R, Riedl S, Ahmed SF, Juul A. Ljubicic ML, et al. Among authors: hiort o. J Clin Endocrinol Metab. 2019 Dec 1;104(12):5812-5813. doi: 10.1210/jc.2019-01413. J Clin Endocrinol Metab. 2019. PMID: 31276168 No abstract available.

2

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

3

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

4

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

5

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

6

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.

7

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

8

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

9

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

10

The molecular basis of male sexual differentiation.

Hiort O, Holterhus PM. Hiort O, et al. Eur J Endocrinol. 2000 Feb;142(2):101-10. doi: 10.1530/eje.0.1420101. Eur J Endocrinol. 2000. PMID: 10664515 Review.

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