Melegh B - Search Results

1

Increased prevalence of glycoprotein IIb/IIIa Leu33Pro polymorphism in term infants with grade I intracranial haemorrhage.

Havasi V, Komlósi K, Bene J, Melegh B. Havasi V, et al. Among authors: melegh b. Neuropediatrics. 2006 Apr;37(2):67-71. doi: 10.1055/s-2006-923980. Neuropediatrics. 2006. PMID: 16773503

2

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: melegh b. Biol Neonate. 2005;87(1):56-9. doi: 10.1159/000081244. Epub 2004 Sep 30. Biol Neonate. 2005. PMID: 15467293

3

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: melegh b, melegh g. Acta Haematol. 2003;110(4):220-2. doi: 10.1159/000074233. Acta Haematol. 2003. PMID: 14663173 No abstract available.

4

No influence of SLC22A4 C6607T and RUNX1 G24658C genotypic variants on the circulating carnitine ester profile in patients with rheumatoid arthritis.

Komlósi K, Talián GC, Faragó B, Magyari L, Cserép V, Kovács B, Bene J, Havasi V, Kiss CG, Czirják L, Melegh B. Komlósi K, et al. Among authors: melegh b. Clin Exp Rheumatol. 2008 Jan-Feb;26(1):61-6. Clin Exp Rheumatol. 2008. PMID: 18328148

5

Differences in circulating carnitine status of preterm infants fed fortified human milk or preterm infant formula.

Bene J, Komlósi K, Melegh BI, Decsi T, Koletzko B, Sauerwald U. Bene J, et al. Among authors: melegh bi. J Pediatr Gastroenterol Nutr. 2013 Nov;57(5):673-6. doi: 10.1097/MPG.0b013e31829fad06. J Pediatr Gastroenterol Nutr. 2013. PMID: 23783025 Clinical Trial.

6

Plasma carnitine ester profiles in Crohn's disease and ulcerative colitis patients with different IGR2230a_1 genotypes.

Talián G, Lakner L, Bene J, Komlósi K, Horváth K, Gasztonyi B, Miheller P, Figler M, Mózsik G, Tulassay Z, Melegh B. Talián G, et al. Among authors: melegh b. Int J Immunogenet. 2009 Dec;36(6):329-35. doi: 10.1111/j.1744-313X.2009.00834.x. Epub 2009 Sep 7. Int J Immunogenet. 2009. PMID: 19735486

7

Plasma carnitine ester profile in homozygous and heterozygous OCTN2 deficiency.

Komlósi K, Magyari L, Talián GC, Nemes E, Káposzta R, Mogyorósy G, Méhes K, Melegh B. Komlósi K, et al. Among authors: melegh b. J Inherit Metab Dis. 2009 Dec;32 Suppl 1:S15-9. doi: 10.1007/s10545-009-0926-1. Epub 2009 Feb 24. J Inherit Metab Dis. 2009. PMID: 19238580

8

Non-syndromic Hearing Impairment in a Hungarian Family with the m.7510T>C Mutation of Mitochondrial tRNA(Ser(UCN)) and Review of Published Cases.

Komlósi K, Maász A, Kisfali P, Hadzsiev K, Bene J, Melegh BI, Melegh B, Ablonczy M, Németh K, Fekete G. Komlósi K, et al. Among authors: melegh b, melegh bi. JIMD Rep. 2013;9:105-111. doi: 10.1007/8904_2012_187. Epub 2012 Nov 2. JIMD Rep. 2013. PMID: 23430555 Free PMC article.

9

Endothelial nitric oxide synthase gene interactions and the risk of ischaemic stroke.

Szolnoki Z, Havasi V, Bene J, Komlósi K, Szöke D, Somogyvári F, Kondacs A, Szabó M, Fodor L, Bodor A, Gáti I, Wittman I, Melegh B. Szolnoki Z, et al. Among authors: melegh b. Acta Neurol Scand. 2005 Jan;111(1):29-33. doi: 10.1111/j.1600-0404.2004.00345.x. Acta Neurol Scand. 2005. PMID: 15595935

10

Erratum to: Non-syndromic Hearing Impairment in a Hungarian Family with the m.7510T>C Mutation of Mitochondrial tRNA(Ser(UCN)) and Review of Published Cases.

Komlósi K, Maász A, Kisfali P, Hadzsiev K, Bene J, Melegh BI, Ablonczy M, Németh K, Fekete G, Melegh B. Komlósi K, et al. Among authors: melegh b, melegh bi. JIMD Rep. 2013;9:E1. doi: 10.1007/978-3-642-35518-9_195. Epub 2012 Nov 2. JIMD Rep. 2013. PMID: 23832234 Free PMC article. No abstract available.

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