Erdos M - Search Results

1

Recurrent CXCR4 sequence variation in a girl with WHIM syndrome.

Alapi K, Erdos M, Kovács G, Maródi L. Alapi K, et al. Among authors: erdos m. Eur J Haematol. 2007 Jan;78(1):86-8. doi: 10.1111/j.1600-0609.2006.00779.x. Epub 2006 Nov 6. Eur J Haematol. 2007. PMID: 17087743

2

[Disorders of interferon-gamma activation pathways: new group of primary immune deficiency diseases].

Erdös M, Maródi L. Erdös M, et al. Orv Hetil. 2001 Nov 18;142(46):2557-61. Orv Hetil. 2001. PMID: 11770174 Review. Hungarian.

3

[Presenting signs and symptoms in Gaucher disease].

Erdös M, Tóth J, Maródi L. Erdös M, et al. Orv Hetil. 2002 Oct 13;143(41):2327-35. Orv Hetil. 2002. PMID: 12434734 Review. Hungarian.

4

Rebound hepatosplenomegaly in type 1 Gaucher disease.

Tóth J, Erdos M, Maródi L. Tóth J, et al. Among authors: erdos m. Eur J Haematol. 2003 Feb;70(2):125-8. doi: 10.1034/j.1600-0609.2003.00010.x. Eur J Haematol. 2003. PMID: 12581195

5

[Rapidly developing bone destruction in a patient with type 1 Gaucher disease].

Boda A, Erdós M, Tóth J, Nagy J, Maródi L. Boda A, et al. Among authors: erdos m. Orv Hetil. 2003 Mar 30;144(13):625-7. Orv Hetil. 2003. PMID: 12728788 Hungarian.

6

Glucocerebroside inhibits NADPH oxidase activation in cell-free system.

Moskwa P, Palicz A, Paclet MH, Dagher MC, Erdos M, Maródi L, Ligeti E. Moskwa P, et al. Among authors: erdos m. Biochim Biophys Acta. 2004 Apr 5;1688(3):197-203. doi: 10.1016/j.bbadis.2003.12.002. Biochim Biophys Acta. 2004. PMID: 15062869 Free article.

7

[Necrotising fasciitis in hyper-IgE syndrome].

Erdos M, Nagy L, Szentkereszty Z, Sáfrány G, Maródi L. Erdos M, et al. Orv Hetil. 2004 Jun 27;145(26):1367-72. Orv Hetil. 2004. PMID: 15384746 Review. Hungarian.

8

Genetically acquired class-switch recombination defects: the multi-faced hyper-IgM syndrome.

Erdos M, Durandy A, Maródi L. Erdos M, et al. Immunol Lett. 2005 Feb 15;97(1):1-6. doi: 10.1016/j.imlet.2004.09.021. Immunol Lett. 2005. PMID: 15626470 Review. No abstract available.

9

Characterization of a new disease-causing mutation of SH2D1A in a family with X-linked lymphoproliferative disease.

Erdõs M, Uzvölgyi E, Nemes Z, Török O, Rákóczi E, Went-Sümegi N, Sümegi J, Maródi L. Erdõs M, et al. Hum Mutat. 2005 May;25(5):506. doi: 10.1002/humu.9339. Hum Mutat. 2005. PMID: 15841490

10

Megadolichobasilar anomaly with thrombosis in a family with Fabry's disease and a novel mutation in the alpha-galactosidase A gene.

Garzuly F, Maródi L, Erdös M, Grubits J, Varga Z, Gelpi E, Rohonyi B, Mázló M, Molnár A, Budka H. Garzuly F, et al. Among authors: erdos m. Brain. 2005 Sep;128(Pt 9):2078-83. doi: 10.1093/brain/awh546. Epub 2005 Jun 9. Brain. 2005. PMID: 15947062

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