Andrikovics H - Search Results

1

Medium-sized FLT3 internal tandem duplications confer worse prognosis than short and long duplications in a non-elderly acute myeloid leukemia cohort.

Koszarska M, Meggyesi N, Bors A, Batai A, Csacsovszki O, Lehoczky E, Adam E, Kozma A, Lovas N, Sipos A, Krahling T, Dolgos J, Remenyi P, Fekete S, Masszi T, Tordai A, Andrikovics H. Koszarska M, et al. Among authors: andrikovics h. Leuk Lymphoma. 2014 Jul;55(7):1510-7. doi: 10.3109/10428194.2013.850163. Epub 2013 Nov 25. Leuk Lymphoma. 2014. PMID: 24090502

2

[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.

3

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

4

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

5

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

6

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

7

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

8

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

9

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.

10

The role of the human ABCG2 multidrug transporter and its variants in cancer therapy and toxicology.

Cervenak J, Andrikovics H, Ozvegy-Laczka C, Tordai A, Német K, Váradi A, Sarkadi B. Cervenak J, et al. Among authors: andrikovics h. Cancer Lett. 2006 Mar 8;234(1):62-72. doi: 10.1016/j.canlet.2005.01.061. Epub 2005 Dec 7. Cancer Lett. 2006. PMID: 16337740 Review.

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