Bene J - Search Results

1

Significant interethnic differencies in functional variants of PON1 and P2RY12 genes in Roma and Hungarian population samples.

Janicsek I, Sipeky C, Bene J, Duga B, Melegh BI, Sümegi K, Jaromi L, Magyari L, Melegh B. Janicsek I, et al. Among authors: bene j. Mol Biol Rep. 2015 Jan;42(1):227-32. doi: 10.1007/s11033-014-3762-9. Epub 2014 Oct 9. Mol Biol Rep. 2015. PMID: 25297118

2

Congenital cataract as the first symptom of a neuromuscular disease caused by a novel single large-scale mitochondrial DNA deletion.

Bene J, Nádasi E, Kosztolányi G, Méhes K, Melegh B. Bene J, et al. Eur J Hum Genet. 2003 May;11(5):375-9. doi: 10.1038/sj.ejhg.5200975. Eur J Hum Genet. 2003. PMID: 12734542

3

Mapping of possible laminin binding sites of Y. pestis plasminogen activator (Pla) via phage display.

Benedek O, Bene J, Melegh B, Emödy L. Benedek O, et al. Among authors: bene j. Adv Exp Med Biol. 2003;529:101-4. doi: 10.1007/0-306-48416-1_18. Adv Exp Med Biol. 2003. PMID: 12756736

4

Increased prevalence of platelet glycoprotein IIb/IIIa PLA2 allele in ischaemic stroke associated with large vessel pathology.

Szolnoki Z, Somogyvári F, Kondacs A, Szabó M, Bene J, Havasi V, Komlósi K, Melegh B. Szolnoki Z, et al. Among authors: bene j. Thromb Res. 2003 Mar 15;109(5-6):265-9. doi: 10.1016/s0049-3848(03)00258-5. Thromb Res. 2003. PMID: 12818249

5

Search for factor V Arg306 Cambridge and Hong Kong mutations in mixed Hungarian population samples.

Komlósi K, Havasi V, Bene J, Ghosh M, Szolnoki Z, Melegh G, Nagy A, Stankovics J, Császár A, Papp E, Gasztonyi B, Tóth K, Mózsik G, Romics L, ten Cate H, Smits P, Méhes K, Kosztolányi G, Melegh B. Komlósi K, et al. Among authors: bene j. Acta Haematol. 2003;110(4):220-2. doi: 10.1159/000074233. Acta Haematol. 2003. PMID: 14663173 No abstract available.

6

Molecular epidemiology of human P[8],G9 rotaviruses in Hungary between 1998 and 2001.

Bányai K, Gentsch JR, Schipp R, Jakab F, Bene J, Melegh B, Glass RI, Szücs G. Bányai K, et al. Among authors: bene j. J Med Microbiol. 2004 Aug;53(Pt 8):791-801. doi: 10.1099/jmm.0.45603-0. J Med Microbiol. 2004. PMID: 15272068

7

Increased prevalence of factor V Leiden mutation in premature but not in full-term infants with grade I intracranial haemorrhage.

Komlósi K, Havasi V, Bene J, Storcz J, Stankovics J, Mohay G, Weisenbach J, Kosztolányi G, Melegh B. Komlósi K, et al. Among authors: bene j. Biol Neonate. 2005;87(1):56-9. doi: 10.1159/000081244. Epub 2004 Sep 30. Biol Neonate. 2005. PMID: 15467293

8

Phenotypic manifestations of the OCTN2 V295X mutation: sudden infant death and carnitine-responsive cardiomyopathy in Roma families.

Melegh B, Bene J, Mogyorósy G, Havasi V, Komlósi K, Pajor L, Oláh E, Kispál G, Sumegi B, Méhes K. Melegh B, et al. Among authors: bene j. Am J Med Genet A. 2004 Dec 1;131(2):121-6. doi: 10.1002/ajmg.a.30207. Am J Med Genet A. 2004. PMID: 15487009

9

[Phenotypic variants of A3243G mitochondrial DNA mutation in a Hungarian family].

Komlósi K, Bene J, Havasi V, Tihanyi M, Herczegfalvi A, Móser J, Melegh B. Komlósi K, et al. Among authors: bene j. Orv Hetil. 2004 Aug 29;145(35):1805-9. Orv Hetil. 2004. PMID: 15493224 Hungarian.

10

Glycoprotein IIIA gene (PlA) polymorphism and aspirin resistance: is there any correlation?

Papp E, Havasi V, Bene J, Komlosi K, Czopf L, Magyar E, Feher C, Feher G, Horvath B, Marton Z, Alexy T, Habon T, Szabo L, Toth K, Melegh B. Papp E, et al. Among authors: bene j. Ann Pharmacother. 2005 Jun;39(6):1013-8. doi: 10.1345/aph.1E227. Epub 2005 Apr 19. Ann Pharmacother. 2005. PMID: 15840736

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