Boehmer A - Search Results

1

Leydig cell hypoplasia: cases with new mutations, new polymorphisms and cases without mutations in the luteinizing hormone receptor gene.

Richter-Unruh A, Martens JW, Verhoef-Post M, Wessels HT, Kors WA, Sinnecker GH, Boehmer A, Drop SL, Toledo SP, Brunner HG, Themmen AP. Richter-Unruh A, et al. Among authors: boehmer a. Clin Endocrinol (Oxf). 2002 Jan;56(1):103-12. doi: 10.1046/j.0300-0664.2001.01437.x. Clin Endocrinol (Oxf). 2002. PMID: 11849253

2

Androgen receptor mutations.

Brinkmann AO, Jenster G, Ris-Stalpers C, van der Korput JA, Brüggenwirth HT, Boehmer AL, Trapman J. Brinkmann AO, et al. Among authors: boehmer al. J Steroid Biochem Mol Biol. 1995 Jun;53(1-6):443-8. doi: 10.1016/0960-0760(95)00090-m. J Steroid Biochem Mol Biol. 1995. PMID: 7626493 Free article. Review.

3

Molecular basis of androgen insensitivity.

Brüggenwirth HT, Boehmer AL, Verleun-Mooijman MC, Hoogenboezem T, Kleijer WJ, Otten BJ, Trapman J, Brinkmann AO. Brüggenwirth HT, et al. Among authors: boehmer al. J Steroid Biochem Mol Biol. 1996 Aug;58(5-6):569-75. doi: 10.1016/0960-0760(96)00095-7. J Steroid Biochem Mol Biol. 1996. PMID: 8918984

4

Germ-line and somatic mosaicism in the androgen insensitivity syndrome: implications for genetic counseling.

Boehmer AL, Brinkmann AO, Niermeijer MF, Bakker L, Halley DJ, Drop SL. Boehmer AL, et al. Am J Hum Genet. 1997 Apr;60(4):1003-6. Am J Hum Genet. 1997. PMID: 9106550 Free PMC article. No abstract available.

5

Substitution of Ala564 in the first zinc cluster of the deoxyribonucleic acid (DNA)-binding domain of the androgen receptor by Asp, Asn, or Leu exerts differential effects on DNA binding.

Brüggenwirth HT, Boehmer AL, Lobaccaro JM, Chiche L, Sultan C, Trapman J, Brinkmann AO. Brüggenwirth HT, et al. Among authors: boehmer al. Endocrinology. 1998 Jan;139(1):103-10. doi: 10.1210/endo.139.1.5696. Endocrinology. 1998. PMID: 9421404 Free article.

6

17Beta-hydroxysteroid dehydrogenase-3 deficiency: diagnosis, phenotypic variability, population genetics, and worldwide distribution of ancient and de novo mutations.

Boehmer AL, Brinkmann AO, Sandkuijl LA, Halley DJ, Niermeijer MF, Andersson S, de Jong FH, Kayserili H, de Vroede MA, Otten BJ, Rouwé CW, Mendonça BB, Rodrigues C, Bode HH, de Ruiter PE, Delemarre-van de Waal HA, Drop SL. Boehmer AL, et al. J Clin Endocrinol Metab. 1999 Dec;84(12):4713-21. doi: 10.1210/jcem.84.12.6174. J Clin Endocrinol Metab. 1999. PMID: 10599740

7

Androgen insensitivity syndrome (AIS): emotional reactions of parents and adult patients to the clinical diagnosis of AIS and its confirmation by androgen receptor gene mutation analysis.

Slijper FM, Frets PG, Boehmer AL, Drop SL, Niermeijer MF. Slijper FM, et al. Among authors: boehmer al. Horm Res. 2000;53(1):9-15. doi: 10.1159/000023506. Horm Res. 2000. PMID: 10965214

8

Phenotypic variation in a family with partial androgen insensitivity syndrome explained by differences in 5alpha dihydrotestosterone availability.

Boehmer AL, Brinkmann AO, Nijman RM, Verleun-Mooijman MC, de Ruiter P, Niermeijer MF, Drop SL. Boehmer AL, et al. J Clin Endocrinol Metab. 2001 Mar;86(3):1240-6. doi: 10.1210/jcem.86.3.7333. J Clin Endocrinol Metab. 2001. PMID: 11238515

9

Etiological studies of severe or familial hypospadias.

Boehmer AL, Nijman RJ, Lammers BA, de Coninck SJ, Van Hemel JO, Themmen AP, Mureau MA, de Jong FH, Brinkmann AO, Niermeijer MF, Drop SL. Boehmer AL, et al. J Urol. 2001 Apr;165(4):1246-54. J Urol. 2001. PMID: 11257695

10

[Differential diagnosis and treatment of girls with 46XY-karyotype and androgen insensitivity syndrome].

Drop SL, Boehmer AL, Slijper FM, Nijman JM, Hazebroek FW, Niermeijer MF. Drop SL, et al. Among authors: boehmer al. Ned Tijdschr Geneeskd. 2001 Apr 7;145(14):665-9. Ned Tijdschr Geneeskd. 2001. PMID: 11530701 Review. Dutch.

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