Andrikovics H - Search Results

1

IGH::NSD2 Fusion Gene Transcript as Measurable Residual Disease Marker in Multiple Myeloma.

Bors A, Kozma A, Tomán Á, Őrfi Z, Kondor N, Tasnády S, Vályi-Nagy I, Reményi P, Mikala G, Andrikovics H. Bors A, et al. Among authors: andrikovics h. Cancers (Basel). 2024 Jan 9;16(2):283. doi: 10.3390/cancers16020283. Cancers (Basel). 2024. PMID: 38254774 Free PMC article.

2

ATG16L1 and IL23 receptor (IL23R) genes are associated with disease susceptibility in Hungarian CD patients.

Lakatos PL, Szamosi T, Szilvasi A, Molnar E, Lakatos L, Kovacs A, Molnar T, Altorjay I, Papp M, Tulassay Z, Miheller P, Papp J, Tordai A, Andrikovics H; Hungarian IBD Study Group. Lakatos PL, et al. Among authors: andrikovics h. Dig Liver Dis. 2008 Nov;40(11):867-73. doi: 10.1016/j.dld.2008.03.022. Epub 2008 May 22. Dig Liver Dis. 2008. PMID: 18499543

3

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.

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: andrikovics h. 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

Anti-microbial antibodies in celiac disease: trick or treat?

Papp M, Foldi I, Altorjay I, Palyu E, Udvardy M, Tumpek J, Sipka S, Korponay-Szabo IR, Nemes E, Veres G, Dinya T, Tordai A, Andrikovics H, Norman GL, Lakatos PL. Papp M, et al. Among authors: andrikovics h. World J Gastroenterol. 2009 Aug 21;15(31):3891-900. doi: 10.3748/wjg.15.3891. World J Gastroenterol. 2009. PMID: 19701969 Free PMC article.

6

Model system for the analysis of cell surface expression of human ABCA1.

Kasza I, Hegyi Z, Szabó K, Andrikovics H, Német K, Váradi A, Sarkadi B, Homolya L. Kasza I, et al. Among authors: andrikovics h. BMC Cell Biol. 2009 Dec 21;10:93. doi: 10.1186/1471-2121-10-93. BMC Cell Biol. 2009. PMID: 20025763 Free PMC article.

7

[A case of hemochromatosis diagnosed in a middle-aged patient with diabetes mellitus].

Wagner R, Tabák A, Bálint Z, Andrikovics H, Tordai A, Demeter J. Wagner R, et al. Among authors: andrikovics h. Orv Hetil. 2006 Jun 25;147(25):1179-84. Orv Hetil. 2006. PMID: 16893134 Hungarian.

8

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.

9

Hemochromatosis gene mutation--could it be a disease marker for myelodysplasia?

Várkonyi J, Andrikovics H, Tordai A. Várkonyi J, et al. Among authors: andrikovics h. Leuk Res. 2009 Jan;33(1):201-2. doi: 10.1016/j.leukres.2008.03.030. Epub 2008 May 6. Leuk Res. 2009. PMID: 18462792 No abstract available.

10

Homogeneous assay based on 52 primer sets to scan for mutations of the ABCA1 gene and its application in genetic analysis of a new patient with familial high-density lipoprotein deficiency syndrome.

Lapicka-Bodzioch K, Bodzioch M, Krüll M, Kielar D, Probst M, Kiec B, Andrikovics H, Böttcher A, Hubacek J, Aslanidis C, Suttorp N, Schmitz G. Lapicka-Bodzioch K, et al. Among authors: andrikovics h. Biochim Biophys Acta. 2001 Jul 27;1537(1):42-8. doi: 10.1016/s0925-4439(01)00053-9. Biochim Biophys Acta. 2001. PMID: 11476961 Free article.

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