Search Results - "Komlósi, K."

Mutations of the apolipoprotein A5 gene with inherited hypertriglyceridaemia: review of the current literature by Melegh, B I, Duga, B, Sümegi, K, Kisfali, P, Maász, A, Komlósi, K, Hadzsiev, K, Komoly, S, Kosztolányi, G, Melegh, B

“…Apoliporotein A5 (APOA5), a member of the apolipoprotein family, plays a key regulatory role in triglyceride (TG) metabolism. Even though the exact biochemical…”
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Endothelial nitric oxide synthase gene interactions and the risk of ischaemic stroke by 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.

“…Objective– Endothelial nitric oxide synthase (eNOS), which produces NO, plays an important role in the endothelial function under a wide range of physiological…”
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Plasma carnitine ester profile in homozygous and heterozygous OCTN2 deficiency by Komlósi, K., Magyari, L., Talián, G. C., Nemes, É., Káposzta, R., Mogyorósy, G., Méhes, K., Melegh, B.

“…Summary The carnitine ester spectrum was studied using ESI tandem mass spectrometry in a 2.5-year-old male Roma child with homozygous deletion of 844C of the…”
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Increased prevalence of glycoprotein IIb/IIIa Leu33Pro polymorphism in term infants with grade I intracranial haemorrhage by Havasi, V, Komlósi, K, Bene, J, Melegh, B

“…The prevalence rates of the platelet glycoprotein IIb/IIIa Leu33Pro allele (PLA2), and factor V G1691A Leiden mutation were determined in 109 appropriate for…”
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Plasma carnitine ester profiles in Crohn's disease and ulcerative colitis patients with different IGR2230a_1 genotypes by Talián, G., Lakner, L., Bene, J., Komlósi, K., Horváth, K., Gasztonyi, B., Miheller, P., Figler, M., Mózsik, G., Tulassay, Z., Melegh, B.

“…Summary An association has been repeatedly demonstrated between inflammatory bowel disease (IBD) and the IBD5 locus in the 5q31 chromosomal region. The aim of…”
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Quality of life and clinical characteristics of self‐improving congenital ichthyosis within the disease spectrum of autosomal‐recessive congenital ichthyosis by Hake, L., Süßmuth, K., Komlosi, K., Kopp, J., Drerup, C., Metze, D., Traupe, H., Hausser, I., Eckl, K.M., Hennies, H.C., Fischer, J., Oji, V.

“…Background Autosomal‐recessive congenital ichthyosis (ARCI) is a heterogeneous group of ichthyoses presenting at birth. Self‐improving congenital ichthyosis…”
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No influence of SLC22A4 C6607T and RUNX1 G24658C genotypic variants on the circulating carnitine ester profile in patients with rheumatoid arthritis by KOMLOSI, K, TALIAN, G. C, MELEGH, B, FARAGO, B, MAGYARI, L, CSEREP, V, KOVACS, B, BENE, J, HAVASI, V, KISS, C. G, CZIRJAK, L

“…In a Japanese study, the C6607T SNP mapping to intron 1 of the SLC22A4 gene encoding the OCTN1 protein was found to be associated with rheumatoid arthritis…”
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Increased prevalence of factor V Leiden mutation in premature but not in full-term infants with grade I intracranial haemorrhage by Komlósi, K, Havasi, V, Bene, J, Storcz, J, Stankovics, J, Mohay, G, Weisenbach, J, Kosztolányi, G, Melegh, B

“…In the current prospective study our aim was to analyse the distribution of the factor V Leiden (G1691A) mutation in preterm and full-term neonates with grade…”
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A retrospective study on the liver toxicity of oral retinoids in Chanarin–Dorfman syndrome by Valette, C., Jonca, N., Fischer, J., Pernin‐Grandjean, J., Granier Tournier, C., Diociaiuti, A., Neri, I., Dreyfus, I., Furman, M., Giehl, K., Wollenberg, A., Mallet, S., Martin, L., Martin‐Santiago, A., Onnis, G., Broue, P., Leclerc‐Mercier, S., Schmuth, M., Sprecher, E., Gruber, R., Suessmuth, K., Bourrat, E., Komlosi, K., Hill, S., O'Toole, E. A., Schischmanoff, O., Caux, F., Mazereeuw‐Hautier, J.

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EPH163 Dental Preventive Examinations and Caries Prevalence in Children Aged 8-14 Years by Bebesi, D., Csákvári, T., Karácsony, I., Komlósi, K., Szabó, L., Boncz, I., Pakai, A.

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EPH218 Knowledge of Contraception and Sexually Transmitted Diseases Regarding the Quality of Education and Parent-Child Relationship Among Secondary School Students by Karácsony, I., Kiss, R.S., Csákvári, T., Ferenczy, M., Komlósi, K., Kiss, Z., Boncz, I., Pakai, A.

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PCR276 Difficulties of Elimination Diets - Experiences of Allergy / Intolerance Among Young Adults by Pergel, M, Kovács, E, Csákvári, T, Takács, K, Ferenczy, M, Komlósi, K, Boncz, I, Karácsony, I

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PCR277 Nutritional Status Assessment in Patients With Lung Cancer by Szabó, A, Szabó, L, Ferenczy, M, Komlósi, K, Sántha, E, Pergel, M, Boncz, I, Pakai, A

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EPH27 Examining the Risk Behaviour of Young People by Ferenczy, M, Szabó, D, Prémusz, V, Komlósi, K, Rozmann, N, Boncz, I, Pakai, A, Karácsony, I

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EPH79 Examining the Health Behaviour of Young People by Ferenczy, M, Szabó, D, Komlósi, K, Rozmann, N, Grasselly, M, Pergel, M, Boncz, I, Karácsony, I

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PCR215 Quality of Life Study of Adult Population With Inflammatory Bowel Disease by Baráth, B, Komlósi, K, Karácsony, I, Pakai, A, Grasselly, M, Kozmann, K, Boncz, I, Ferenczy, M

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CO143 Impact of Perinatal Loss on Midwives by Komlósi, K, Sinka, B, Karácsony, I, Pakai, A, Boncz, I, Pergel, M, Sántha, E, Ferenczy, M

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PCR19 Dental Preventive Screenings and Caries Prevalence in the Age Group of 13-15 by Hegedűs, B, Rácz, V, Sugár, M, Rozmann, N, Karácsony, I, Komlósi, K, Boncz, I, Pakai, A

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PCR120 Assessing the Quality of Life of Children with Asthma Bronchiale by Kelemen, G, Csákvári, T, Kozmann, K, Karácsony, I, Rozmann, N, Komlósi, K, Boncz, I, Pakai, A

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PCR159 Assessment of Antenatal Anxiety Among Gravidas by Karácsony, I, Horváth, L, Csákvári, T, Komlósi, K, Bornemisza, Á, Varga, B, Boncz, I, Pakai, A

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