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References [1]. P. Malhotra R. Kchhar N. Varma 2000 Patterson-Kelly Syndrome and celiac disease-a rare combination Indian J. Gastroenterol. 19 191 – 192 . [2]. A. Sood V. Midha N. Sood 2003 Adult celiac

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Orvosi Hetilap
Authors: Dorottya Kocsis, Nóra Béres, Gábor Veres, Dolóresz Szabó, Katalin Eszter Müller, András Arató, and Márk Juhász

Husby, S., Koletzko, S., Korponay-Szabó, I. R., et al.: European Society for Pediatric Gastroenterology, Hepatology, and Nutrition guidelines for the diagnosis of coeliac disease. J. Pediatr

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). Mortality in patients with coeliac disease and their relatives: A cohort study. Lancet, 358, 356—361. de Rosa, A., Troncone, A., Vacca, M., & Ciacci, C. (2004). Characteristics and quality of illness behavior in celiac disease

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Farrell, R. J., Kelly, C. P.: Celiac disease. N. Engl. J. Med., 2002, 346 , 180–88. Kelly C. P. Celiac disease

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Acta Physiologica Hungarica
Authors: L.R. Nikoukar, Fatemeh Nabavizadeh, S.M. Mohamadi, A. Moslehi, G. Hassanzadeh, H. Nahrevanian, and S. Agah

) Hill I.D. Celiac disease and autoimmunity: review and controversies Curr. Allergy Asthma Rep. 2013 13 347 453 Dickson BC, Streutker CJ, Chetty R: Coeliac disease: an update for

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Orvosi Hetilap
Authors: Kriszta Molnár, Ádám Vannay, Erna Sziksz, Nóra Fanni Bánki, Áron Cseh, Hajnalka Győrffy, Antal Dezsőfi, András Arató, and Gábor Veres

., Engelmann, G., Findeisen, A., et al.: Cesarean delivery is associated with celiac disease but not inflammatory bowel disease in children. Pediatrics, 2010, 125 , e1433–e1440. Findeisen A

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Not, T., Horvath, K., Hill, I. D. és mtsai: Celiac disease risk in the USA: high prevalence of antiendomysium antibodies in healthy blood donors. Scand. J. Gastroenterol., 1998, 33 , 494–498. Hill I. D

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.H. , Guandalini , S. , Hill , I.D. , Pietzak , M. , Ventura , A. , Thorpe , M. , Kryszak , D. , Fornaroli , F. , Wasserman , S.S. , Murray , J.A. & Horvath , K. ( 2003 ). Prevalence of coeliac disease in at-risk and not-at-risk groups in the

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Enzyme-linked immunosorbent assays (ELISAs) are widely used to determine gluten contamination in gluten-free and low gluten food samples. ELISA assays developed using monoclonal antibodies against known toxic peptides have an advantage in the identification of toxic prolamin content in protein extracts of different food samples, as well as raw materials. R5 and G12 monoclonal antibodies specific for two known toxic peptides used in commercially available gluten ELISA assays were applied to test toxic peptide contents in wheat relatives and wild wheat species with different genome composition and complexity. Although the R5 peptide content showed some correlation with ploidy levels in Triticum species, there was a high variance among Aegilops species. Some of the analysed diploid Aegilops species showed extremely high R5 peptide contents. Based on the bioinformatics analyses, the R5 peptide was present in most of the sulphur rich prolamins in all the analysed species, whereas the G12 epitope was exclusively present in alpha gliadins. High variation was detected in the position and frequency of epitopes in sequences originating from the same species, thus highlighting the importance of genotypic variation within species. Identification of new prolamin alleles of wheat relatives and wild wheat species is of great importance in order to find germplasm for special end-use quality purposes as well as development of food with reduced toxicity.

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Hungarian Medical Journal
Authors: Anna Körner, Péter Tóth-Heyn, Antal Dezsőfi, Gábor Veres, László Madácsy, and András Arató

405 Paulsen, G., Lundin, K. E., Gjertsen, H. A. et al.: HLA DQ2-restricted T-cell recognition of gluten-derived peptides in celiac disease. Influence of aminoacid substitution

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