Szalai C - Search Results

1

The P28T mutation in the GALK1 gene accounts for galactokinase deficiency in Roma (Gypsy) patients across Europe.

Hunter M, Heyer E, Austerlitz F, Angelicheva D, Nedkova V, Briones P, Gata A, de Pablo R, László A, Bosshard N, Gitzelmann R, Tordai A, Kalmar L, Szalai C, Balogh I, Lupu C, Corches A, Popa G, Perez-Lezaun A, Kalaydjieva LV. Hunter M, et al. Among authors: szalai c. Pediatr Res. 2002 May;51(5):602-6. doi: 10.1203/00006450-200205000-00010. Pediatr Res. 2002. PMID: 11978884

2

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

3

Association of some rare haplotypes and genotype combinations in the MDR1 gene with childhood acute lymphoblastic leukaemia.

Semsei AF, Erdélyi DJ, Ungvári I, Kámory E, Csókay B, Andrikovics H, Tordai A, Cságoly E, Falus A, Kovács GT, Szalai C. Semsei AF, et al. Among authors: szalai c. Leuk Res. 2008 Aug;32(8):1214-20. doi: 10.1016/j.leukres.2007.12.009. Epub 2008 Feb 19. Leuk Res. 2008. PMID: 18243305

4

The role of ABC-transporter gene polymorphisms in chemotherapy induced immunosuppression, a retrospective study in childhood acute lymphoblastic leukaemia.

Erdélyi DJ, Kámory E, Zalka A, Semsei AF, Csókay B, Andrikovics H, Tordai A, Borgulya G, Magyarosy E, Galántai I, Fekete G, Falus A, Szalai C, Kovács GT. Erdélyi DJ, et al. Among authors: szalai c. Cell Immunol. 2006 Dec;244(2):121-4. doi: 10.1016/j.cellimm.2007.02.007. Epub 2007 Apr 16. Cell Immunol. 2006. PMID: 17434155

5

Involvement of TNFalpha -308A promoter polymorphism in the development of asthma in children infected with Chlamydophila pneumoniae.

Tölgyesi G, Keszei M, Ungvári I, Nagy A, Falus A, Szalai C. Tölgyesi G, et al. Among authors: szalai c. Pediatr Res. 2006 Nov;60(5):543-8. doi: 10.1203/01.pdr.0000242298.24089.52. Epub 2006 Sep 20. Pediatr Res. 2006. PMID: 16988194

6

Chemokine receptor CCR2 and CCR5 polymorphisms in children with insulin-dependent diabetes mellitus.

Szalai C, Császár A, Czinner A, Szabó T, Pánczél P, Madácsy L, Falus A. Szalai C, et al. Pediatr Res. 1999 Jul;46(1):82-4. doi: 10.1203/00006450-199907000-00014. Pediatr Res. 1999. PMID: 10400139

7

Synergistic interaction of ABCB1 and ABCG2 polymorphisms predicts the prevalence of toxic encephalopathy during anticancer chemotherapy.

Erdilyi DJ, Kámory E, Csókay B, Andrikovics H, Tordai A, Kiss C, Filni-Semsei A, Janszky I, Zalka A, Fekete G, Falus A, Kovács GT, Szalai C. Erdilyi DJ, et al. Among authors: szalai c. Pharmacogenomics J. 2008 Oct;8(5):321-7. doi: 10.1038/sj.tpj.6500480. Pharmacogenomics J. 2008. PMID: 17938643

8

Frequency of the R3500Q mutation of the apolipoprotein B-100 gene in a sample screened clinically for familial hypercholesterolemia in Hungary.

Kalina A, Császár A, Czeizel AE, Romics L, Szabóki F, Szalai C, Reiber I, Németh A, Stephenson S, Williams RR. Kalina A, et al. Among authors: szalai c. Atherosclerosis. 2001 Jan;154(1):247-51. doi: 10.1016/s0021-9150(00)00648-1. Atherosclerosis. 2001. PMID: 11137107

9

Frequency of carriers of 8.1 ancestral haplotype and its fragments in two Caucasian populations.

Kiszel P, Kovács M, Szalai C, Yang Y, Pozsonyi E, Blaskó B, Laki J, Prohászka Z, Fazakas A, Pánczél P, Hosszúfalusi N, Rajczy K, Wu YL, Chung EK, Zhou B, Blanchong CA, Vatay A, Yu CY, Füst G. Kiszel P, et al. Among authors: szalai c. Immunol Invest. 2007;36(3):307-19. doi: 10.1080/08820130701241404. Immunol Invest. 2007. PMID: 17558713

10

Influence of apolipoprotein E genotypes on serum lipid parameters in a biracial sample of children.

Szalai C, Czinner A, Császár A. Szalai C, et al. Eur J Pediatr. 2000 Apr;159(4):257-60. doi: 10.1007/s004310050065. Eur J Pediatr. 2000. PMID: 10789929

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