Hiort O - Search Results

1

A novel ultrapressure liquid chromatography tandem mass spectrometry method for the simultaneous determination of androstenedione, testosterone, and dihydrotestosterone in pediatric blood samples: age- and sex-specific reference data.

Kulle AE, Riepe FG, Melchior D, Hiort O, Holterhus PM. Kulle AE, et al. Among authors: hiort o. J Clin Endocrinol Metab. 2010 May;95(5):2399-409. doi: 10.1210/jc.2009-1670. Epub 2010 Mar 3. J Clin Endocrinol Metab. 2010. PMID: 20200336

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

Immunohistochemistry and in situ hybridization of the androgen receptor in the developing human prostate.

Aumüller G, Holterhus PM, Konrad L, von Rahden B, Hiort O, Esquenet M, Verhoeven G. Aumüller G, et al. Among authors: hiort o. Anat Embryol (Berl). 1998 Mar;197(3):199-208. doi: 10.1007/s004290050131. Anat Embryol (Berl). 1998. PMID: 9543338

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

Gonadal histology with testicular carcinoma in situ in a 15-year-old 46,XY female patient with a premature termination in the steroidogenic acute regulatory protein causing congenital lipoid adrenal hyperplasia.

Korsch E, Peter M, Hiort O, Sippell WG, Ure BM, Hauffa BP, Bergmann M. Korsch E, et al. Among authors: hiort o. J Clin Endocrinol Metab. 1999 May;84(5):1628-32. doi: 10.1210/jcem.84.5.5694. J Clin Endocrinol Metab. 1999. PMID: 10323391

10

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

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