Andrikovics H - Search Results

1

Characterization of ABL exon 7 deletion by molecular genetic and bioinformatic methods reveals no association with imatinib resistance in chronic myeloid leukemia.

Meggyesi N, Kalmár L, Fekete S, Masszi T, Tordai A, Andrikovics H. Meggyesi N, et al. Among authors: andrikovics h. Med Oncol. 2012 Sep;29(3):2136-42. doi: 10.1007/s12032-011-0092-9. Epub 2011 Oct 30. Med Oncol. 2012. PMID: 22038725

2

High frequency of the haemochromatosis C282Y mutation in Hungary could argue against a Celtic origin of the mutation.

Tordai A, Andrikovics H, Kalmár L, Rajczy K, Pénzes M, Sarkadi B, Klein I, Váradi A. Tordai A, et al. Among authors: andrikovics h. J Med Genet. 1998 Oct;35(10):878-9. doi: 10.1136/jmg.35.10.878-a. J Med Genet. 1998. PMID: 9783719 Free PMC article. No abstract available.

3

[A new method of molecular testing in the differential diagnosis of hereditary hemochromatosis].

Andrikovics H, Klein I, Kalmár L, Bors A, Jermendy G, Petri I, Kalász L, Váradi A, Tordai A. Andrikovics H, et al. Orv Hetil. 1999 Nov 7;140(45):2517-22. Orv Hetil. 1999. PMID: 10586619 Hungarian.

4

Genotype screening for hereditary hemochromatosis among voluntary blood donors in Hungary.

Andrikovics H, Kalmár L, Bors A, Fandl B, Petri I, Kalász L, Tordai A. Andrikovics H, et al. Blood Cells Mol Dis. 2001 Jan-Feb;27(1):334-41. doi: 10.1006/bcmd.2001.0384. Blood Cells Mol Dis. 2001. PMID: 11358395

5

A haemophilia A and B molecular genetic diagnostic programme in Hungary: a highly informative and cost-effective strategy.

Klein I, Andrikovics H, Bors A, Nemes L, Tordai A, Váradi A. Klein I, et al. Among authors: andrikovics h. Haemophilia. 2001 May;7(3):306-12. doi: 10.1046/j.1365-2516.2001.00497.x. Haemophilia. 2001. PMID: 11380636

6

High incidence of hemochromatosis gene mutations in the myelodysplastic syndrome: the Budapest Study on 50 patients.

Várkonyi J, Tarkovács G, Karádi I, Andrikovics H, Varga F, Varga F, Demeter J, Tordai A. Várkonyi J, et al. Among authors: andrikovics h. Acta Haematol. 2003;109(2):64-7. doi: 10.1159/000068487. Acta Haematol. 2003. PMID: 12624489

7

Analysis of large structural changes of the factor VIII gene, involving intron 1 and 22, in severe hemophilia A.

Andrikovics H, Klein I, Bors A, Nemes L, Marosi A, Váradi A, Tordai A. Andrikovics H, et al. Haematologica. 2003 Jul;88(7):778-84. Haematologica. 2003. PMID: 12857556

8

Frequencies of two common mutations (c.35delG and c.167delT) of the connexin 26 gene in different populations of Hungary.

Bors A, Andrikovics H, Kalmár L, Erdei N, Galambos S, Losonczi A, Füredi S, Balogh I, Szalai C, Tordai A. Bors A, et al. Among authors: andrikovics h. Int J Mol Med. 2004 Dec;14(6):1105-8. Int J Mol Med. 2004. PMID: 15547683

9

Asymmetric PCR increases efficiency of melting peak analysis on the LightCycler.

Szilvási A, Andrikovics H, Kalmár L, Bors A, Tordai A. Szilvási A, et al. Among authors: andrikovics h. Clin Biochem. 2005 Aug;38(8):727-30. doi: 10.1016/j.clinbiochem.2005.04.015. Clin Biochem. 2005. PMID: 15982647

10

TNF-alpha promoter gene polymorphism in patients with myelodysplastic syndrome.

Kádár K, Demeter J, Andrikovics H, Tordai A, Kovács M, Fust G, Karádi I, Várkonyi J. Kádár K, et al. Among authors: andrikovics h. Acta Haematol. 2005;113(4):262-4. doi: 10.1159/000084681. Acta Haematol. 2005. PMID: 15983434 No abstract available.

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