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Drug-induced myocardial infarction in young patients: report of two cases.
Papp E, Czopf L, Habon T, Halmosi R, Horvath B, Marton Z, Tahin T, Komocsi A, Horvath I, Melegh B, Toth K. Papp E, et al. Among authors: melegh b. Int J Cardiol. 2005 Jan;98(1):169-70. doi: 10.1016/j.ijcard.2003.12.019. Int J Cardiol. 2005. PMID: 15676187 No abstract available.
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.
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.
Hearing impairment locus heterogeneity and identification of PLS1 as a new autosomal dominant gene in Hungarian Roma.
Schrauwen I, Melegh BI, Chakchouk I, Acharya A, Nasir A, Poston A, Cornejo-Sanchez DM, Szabo Z, Karosi T, Bene J, Melegh B, Leal SM. Schrauwen I, et al. Among authors: melegh b, melegh bi. Eur J Hum Genet. 2019 Jun;27(6):869-878. doi: 10.1038/s41431-019-0372-y. Epub 2019 Mar 14. Eur J Hum Genet. 2019. PMID: 30872814 Free PMC article. Clinical Trial.
441 results