Two New Mutations in the CEL Gene Causing Diabetes and Hereditary Pancreatitis: How to Correctly Identify MODY8 Cases by El Jellas, Khadija, Dušátková, Petra, Haldorsen, Ingfrid S, Molnes, Janne, Tjora, Erling, Johansson, Bente B, Fjeld, Karianne, Johansson, Stefan, Průhová, Štěpánka, Groop, Leif, Löhr, J Matthias, Njølstad, Pål R, Molven, Anders

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Novel glucokinase gene mutation in the first Macedonian family tested for MODY by Kocova, M, Elblova, L, Pruhova, S, Lebl, J, Dusatkova, P

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Substantial proportion of MODY among multiplex families participating in a Type 1 diabetes prediction programme by Petruzelkova, L., Dusatkova, P., Cinek, O., Sumnik, Z., Pruhova, S., Hradsky, O., Vcelakova, J., Lebl, J., Kolouskova, S.

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The dynamic changes of zinc transporter 8 autoantibodies in Czech children from the onset of Type 1 diabetes mellitus by Petruzelkova, L., Ananieva-Jordanova, R., Vcelakova, J., Vesely, Z., Stechova, K., Lebl, J., Dusatkova, P., Sumnik, Z., Coles, R., Powell, M., Furmaniak, J., Rees Smith, B., Kolouskova, S.

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Lack of PAX4 mutations in 53 Czech MODYX families by Dusatkova, P., Vesela, K., Pruhova, S., Lebl, J., Cinek, O.

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HbA1c-based diabetes diagnosis among patients with glucokinase mutation (GCK-MODY) is affected by a genetic variant of glucose-6-phosphatase (G6PC2) by Borowiec, M., Fendler, W., Dusatkova, P., Antosik, K., Pruhova, S., Cinek, O., Mysliwiec, M., Jarosz-Chobot, P., Malecki, M. T., Mlynarski, W.

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Independent mutational events in the hypervariable region of the carboxyl ester lipase gene: Identification of two new CEL-MODY families from Sweden and the Czech Republic by El Jellas, K., Dušátková, P., Molnes, J., Haldorsen, I., Tjora, E., Johansson, B., Fjeld, K., Johansson, S., Ů, Prúhová, Groop, L., Njølstad, P., Molven, A.

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Variants of CARD15, TNFA and PTPN22 and susceptibility to Crohn's disease in the Czech population: high frequency of the CARD15 1007fs by Hradsky, O., Lenicek, M., Dusatkova, P., Bronsky, J., Nevoral, J., Valtrova, V., Kotalova, R., Szitanyi, P., Petro, R., Starzykova, V., Bortlik, M., Vitek, L., Lukas, M., Cinek, O.

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P053 TWO INDEPENDENT ASSOCIATIONS ON THE IBD5 LOCUS WITH CROHN'S DISEASE IN THE CZECH POPULATION by Hradsky, O., Dusatkova, P., Lenicek, M., Bronsky, J., Nevoral, J., Vitek, L., Lukas, M., Cinek, O.

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Clinical and laboratory characteristics of 1179 Czech adolescents evaluated for antibodies to human adenovirus 36 by Aldhoon-Hainerová, I, Zamrazilová, H, Atkinson, R L, Dušátková, L, Sedláčková, B, Hlavatý, P, Lee, Z P, Kunešová, M, Hainer, V

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Adenovirus 36 infection: a role in dietary intake and response to inpatient weight management in obese girls by Zamrazilová, H, Aldhoon-Hainerová, I, Atkinson, R L, Dušátková, L, Sedláčková, B, Lee, Z P, Kunešová, M, Hill, M, Hainer, V

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Genesis of two most prevalent PROP1 gene variants causing combined pituitary hormone deficiency in 21 populations by Dusatkova, Petra, Pfäffle, Roland, Brown, Milton R, Akulevich, Natallia, Arnhold, Ivo J P, Kalina, Maria A, Kot, Karolina, Krzisnik, Ciril, Lemos, Manuel C, Malikova, Jana, Navardauskaite, Ruta, Obermannova, Barbora, Pribilincova, Zuzana, Sallai, Agnes, Stipancic, Gordana, Verkauskiene, Rasa, Cinek, Ondrej, Blum, Werner F, Parks, John S, Austerlitz, Frederic, Lebl, Jan

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Lessons from whole-exome sequencing in MODYX families by Dusatkova, Petra, Fang, Mingyan, Pruhova, Stepanka, Gjesing, Anette P, Cinek, Ondrej, Hansen, Torben, Pedersen, Oluf B, Xu, Xun, Lebl, Jan

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Serum testosterone and SHBG levels before and after weight loss in obese adolescent boys and their relationship to metabolic syndrome--P by Sedlackova, B, Zamrazilova, H, Dusatkova, L, Hlavaty, P, Kunesova, M, Hainer, V

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Association of the FTO variant RS9939609 with metabolic syndrome in overweight/ obese and representative cohorts of Czech adolescents--O by Dusatkova, L, Zamrazilova, H, Sedlackova, B, Vcelak, J, Hlavaty, P, Bendlova, B, Kunesova, M, Hainer, V

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