Deletions removing the last exon of TACSTD1 constitute a distinct class of mutations predisposing to Lynch syndrome von Kovacs, Marietta E, Papp, Janos, Szentirmay, Zoltan, Otto, Szabolcs, Olah, Edith

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Germline MLH1 and MSH2 mutational spectrum including frequent large genomic aberrations in Hungarian hereditary non-polyposis colorectal cancer families: implications for genetic t... von Papp, Janos, Kovacs, Marietta E, Olah, Edith

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High prevalence of germline STK11 mutations in Hungarian Peutz-Jeghers Syndrome patients von Papp, Janos, Kovacs, Marietta Eva, Solyom, Szilvia, Kasler, Miklos, Børresen-Dale, Anne-Lise, Olah, Edith

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Synthesis of and a Comparative Study on the Inhibition of Muscle and Liver Glycogen Phosphorylases by Epimeric Pairs of d-Gluco- and d-Xylopyranosylidene-spiro-(thio)hydantoins and... von Somsák, László, Kovács, László, Tóth, Marietta, Ősz, Erzsébet, Szilágyi, László, Györgydeák, Zoltán, Dinya, Zoltán, Docsa, Tibor, Tóth, Béla, Gergely, Pál

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Oral disease in adults treated with hemodialysis: prevalence, predictors, and association with mortality and adverse cardiovascular events: the rationale and design of the ORAL Dis... von Strippoli, Giovanni F M, Palmer, Suetonia C, Ruospo, Marinella, Natale, Patrizia, Saglimbene, Valeria, Craig, Jonathan C, Pellegrini, Fabio, Petruzzi, Massimo, De Benedittis, Michele, Ford, Pauline, Johnson, David W, Celia, Eduardo, Gelfman, Ruben, Leal, Miguel R, Torok, Marietta, Stroumza, Paul, Bednarek-Skublewska, Anna, Dulawa, Jan, Frantzen, Luc, Ferrari, Juan Nin, del Castillo, Domingo, Hegbrant, Jorgen, Wollheim, Charlotta, Gargano, Letitzia

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