Tordai A - Search Results

1

HFE C282Y mutation as a genetic modifier influencing disease susceptibility for chronic myeloproliferative disease.

Andrikovics H, Meggyesi N, Szilvasi A, Tamaska J, Halm G, Lueff S, Nahajevszky S, Egyed M, Varkonyi J, Mikala G, Sipos A, Kalasz L, Masszi T, Tordai A. Andrikovics H, et al. Among authors: tordai a. Cancer Epidemiol Biomarkers Prev. 2009 Mar;18(3):929-34. doi: 10.1158/1055-9965.EPI-08-0359. Epub 2009 Mar 3. Cancer Epidemiol Biomarkers Prev. 2009. PMID: 19258483

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. 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. Among authors: tordai a. Orv Hetil. 1999 Nov 7;140(45):2517-22. Orv Hetil. 1999. PMID: 10586619 Hungarian.

4

A case of non-HFE juvenile haemochromatosis presenting with adrenocortical insufficiency.

Varkonyi J, Kaltwasser JP, Seidl C, Kollai G, Andrikovics H, Tordai A. Varkonyi J, et al. Among authors: tordai a. Br J Haematol. 2000 Apr;109(1):252-3. doi: 10.1046/j.1365-2141.2000.01987.x. Br J Haematol. 2000. PMID: 10896410 Free article. No abstract available.

5

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. Among authors: tordai a. Blood Cells Mol Dis. 2001 Jan-Feb;27(1):334-41. doi: 10.1006/bcmd.2001.0384. Blood Cells Mol Dis. 2001. PMID: 11358395

6

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: tordai a. Haemophilia. 2001 May;7(3):306-12. doi: 10.1046/j.1365-2516.2001.00497.x. Haemophilia. 2001. PMID: 11380636

7

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: tordai a. Acta Haematol. 2003;109(2):64-7. doi: 10.1159/000068487. Acta Haematol. 2003. PMID: 12624489

8

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. Among authors: tordai a. Haematologica. 2003 Jul;88(7):778-84. Haematologica. 2003. PMID: 12857556

9

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: tordai a. Int J Mol Med. 2004 Dec;14(6):1105-8. Int J Mol Med. 2004. PMID: 15547683

10

Homozygosity for a novel nonsense mutation (G66X) of the HJV gene causes severe juvenile hemochromatosis with fatal cardiomyopathy.

Jánosi A, Andrikovics H, Vas K, Bors A, Hubay M, Sápi Z, Tordai A. Jánosi A, et al. Among authors: tordai a. Blood. 2005 Jan 1;105(1):432. doi: 10.1182/blood-2004-09-3508. Blood. 2005. PMID: 15611318 Free article. No abstract available.

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