Bogdanova N - Search Results

1

Treacher Collins syndrome: clinical implications for the paediatrician--a new mutation in a severely affected newborn and comparison with three further patients with the same mutation, and review of the literature.

Schlump JU, Stein A, Hehr U, Karen T, Möller-Hartmann C, Elcioglu NH, Bogdanova N, Woike HF, Lohmann DR, Felderhoff-Mueser U, Linz A, Wieczorek D. Schlump JU, et al. Among authors: bogdanova n. Eur J Pediatr. 2012 Nov;171(11):1611-8. doi: 10.1007/s00431-012-1776-7. Epub 2012 Jun 23. Eur J Pediatr. 2012. PMID: 22729243 Review.

2

Spectrum of molecular defects and mutation detection rate in patients with mild and moderate hemophilia A.

Bogdanova N, Markoff A, Eisert R, Wermes C, Pollmann H, Todorova A, Chlystun M, Nowak-Göttl U, Horst J. Bogdanova N, et al. Hum Mutat. 2007 Jan;28(1):54-60. doi: 10.1002/humu.20403. Hum Mutat. 2007. PMID: 16972227

3

Spectrum of molecular defects and mutation detection rate in patients with severe hemophilia A.

Bogdanova N, Markoff A, Pollmann H, Nowak-Göttl U, Eisert R, Wermes C, Todorova A, Eigel A, Dworniczak B, Horst J. Bogdanova N, et al. Hum Mutat. 2005 Sep;26(3):249-54. doi: 10.1002/humu.20208. Hum Mutat. 2005. PMID: 16086318

4

Seven novel and four recurrent point mutations in the factor VIII (F8C) gene.

Bogdanova N, Lemcke B, Markoff A, Pollmann H, Dworniczak B, Eigel A, Horst J. Bogdanova N, et al. Hum Mutat. 2002 Jan;19(1):84. doi: 10.1002/humu.9007. Hum Mutat. 2002. PMID: 11754115

5

Prevalence of small rearrangements in the factor VIII gene F8C among patients with severe hemophilia A.

Bogdanova N, Markoff A, Pollmann H, Nowak-Göttl U, Eisert R, Dworniczak B, Eigel A, Horst J. Bogdanova N, et al. Hum Mutat. 2002 Sep;20(3):236-7. doi: 10.1002/humu.9062. Hum Mutat. 2002. PMID: 12204009

6

Mutation detection in the duplicated region of the polycystic kidney disease 1 (PKD1) gene in PKD1-linked Australian families.

McCluskey M, Schiavello T, Hunter M, Hantke J, Angelicheva D, Bogdanova N, Markoff A, Thomas M, Dworniczak B, Horst J, Kalaydjieva L. McCluskey M, et al. Among authors: bogdanova n. Hum Mutat. 2002 Mar;19(3):240-50. doi: 10.1002/humu.10045. Hum Mutat. 2002. PMID: 11857740

7

Autosomal dominant polycystic kidney disease - clinical and genetic aspects.

Bogdanova N, Markoff A, Horst J. Bogdanova N, et al. Kidney Blood Press Res. 2002;25(5):265-83. doi: 10.1159/000066788. Kidney Blood Press Res. 2002. PMID: 12435872 Review.

8

Influence of factor 5 rs6025 and factor 2 rs1799963 mutation on inhibitor development in patients with hemophilia A--an Israeli-German multicenter database study.

Kenet G, Bidlingmaier C, Bogdanova N, Ettingshausen CE, Goldenberg N, Gutsche S, Halimeh S, Holzhauer S, Kurnik K, Limperger V, Junker R, Nowak-Göttl U. Kenet G, et al. Among authors: bogdanova n. Thromb Res. 2014 Apr;133(4):544-9. doi: 10.1016/j.thromres.2014.01.005. Epub 2014 Jan 17. Thromb Res. 2014. PMID: 24485400 Free article.

9

Hereditary thrombophilic risk factors for recurrent pregnancy loss.

Bogdanova N, Markoff A. Bogdanova N, et al. J Community Genet. 2010 Jun;1(2):47-53. doi: 10.1007/s12687-010-0011-3. Epub 2010 Jun 11. J Community Genet. 2010. PMID: 22460204 Free PMC article.

10

Haplotypes and polymorphisms of the ANXA5 nontranslated region in Japanese and European women with recurrent miscarriage and in controls.

Markoff A, Bogdanova N. Markoff A, et al. Among authors: bogdanova n. Fertil Steril. 2014 Jan;101(1):e1. doi: 10.1016/j.fertnstert.2013.10.016. Epub 2013 Nov 12. Fertil Steril. 2014. PMID: 24238274 Free article. No abstract available.

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