Csaba Gábor Talián

Talián, G. C., B. Melegh, V. Jakobik, A. Tárnok, T. Decsi. Plasma carnitine ester profiles in children with coeliac disease. Proc. Nutr. Soc., 2007, 66, 18A.

Talian, G. C., K. Komlosi, L. Magyari, E. Nemes, R. Kaposzta, G. Mogyorosy, K. Mehes, B. Melegh. Investigation of plasma carnitine ester profiles in a family with homozygous and heterozygous OCTN2 deficiency. Eur. J. Hum. Genet., 2007, 15(1), 216.

Szabó, J., J. Szöllősi, A. Pál, K. Komlósi, J. Bene, V. Havasi, G. Talián, B. Melegh, Z. László. AZF deletions, MTHFR C677T gene polymorphism and OCTN2 mutation analysis in male infertility. Eur. J. Hum. Gen. 2006, 14(1), 125.

Talián, G. C., K. Horvátovich, A. Maász, L. Magyari, T. Illés, B. Melegh. New polymorphisms in the filaminB gene: novel candidates for causing disease. Eur. J. Hum. Gen. 2006, 14(1), 695.

Havasi, V., Z. Szolnoki, G. Talián, J. Bene, K. Komlósi, A. Maász, F. Somogyvári, A. Kondacs, M. Szabó, L. Fodor, A. Bodor, B. Melegh. Apolipoprotein A5 gene promoter T- 1131C polymorphism associates with elevated triglyceride levels and confers susceptibility for ischaemic stroke. Eur. J. Hum. Gen. 2006, 14(1), 855.

Faragó, B., G. Talián, A. Maász, L. Magyari, K. Horvátovich, B. Kovács, V. Cserép, P. Kisfali, C. Kiss, B. Melegh. Padi4_89*G/A, padi4_90*T/C and padi4_92*G/C SNPs in the gene of the peptidylarginine deiminase citrullinating enzyme type 4 (PADI4) are not associated with rheumatoid arthritis in Hungarian patients. Eur. J. Hum. Gen. 2006, 14(1), 125.

Faragó, B., Cs. G. Talián, A. Maász, L. Magyari, K. Horvatovich, B. Kovács, V. Cserép, P. Kisfali, Cs. Kiss, L. Czirják, B. Melegh. A peptidilarginin deimináz enzimet kódoló gén funkcionális haplotípusainak gyakorisága rheumatoid arthritis betegekben. Klin. Kísérl. Lab. Med., 2006, (S-32), 101.

Talián, G. C., B. Kovács, V. Cserép, J. Bene, K. Komlósi, V. Havasi, L. Czirják, B. Melegh. Prevalence of SLC22A4 and RUNX susceptibility SNPs in rheumatic arthritis patients. Eur. J. Hum. Gen. 2005, 13(1), 892.

Havasi, V., J. Bene, K. Komlósi, B. Gasztonyi, G. C. Talián, V. Cserép, B. Kovács, G. Mózsik, B. Melegh. Screening for two susceptibility-associated polymorphisms of OCTN carnitine transporter in Crohn-desease patients. Eur. J. Hum. Gen. 2005, 13(1), 906.

Horvatovich, K. Z., L. Magyari, A. Maász, G. C. Talián, M. Tamaskó, B. Laczy, I. Wittmann, B. Melegh. Search for mitochondrial DNA T4,291C mutation in Hungarian metabolic syndrome patients. Eur. J. Hum. Gen. 2005, 13(1), 917.

Havasi, V., K. Komlósi, J. Bene, G. Talián, Z. Szolnoki, J, Stankovics, G. Mohay, B. Melegh. Increased prevalence of glycoprotein IIb/IIIa Leu33Pro polymorphism in term infants with grade I intraventricular haemorrhage. Eur. J. Hum. Gen. 2004, 12(1), 915.

Bene, J., G. Mogyorósy, V. Havasi, K. Komlósi, L. Pajor, G. Talián, K. Méhes, B. Melegh. SLC22A5 homozygous 844delC mutation: sudden infant death and carnitine responsive cardiomyopathy on roma families as novel phenotypes of the OCTN2 mutations. Eur. J. Hum. Gen. 2004, 12(1), 678.