Next Generation Sequencing in Molecular Diagnosis of Lynch Syndrome - a Pilot Study Using New Stratification Criteria von Kašubová, Ivana, Holubeková, Veronika, Janíková, Katarína, Váňová, Barbora, Sňahničanová, Zuzana, Kalman, Michal, Plank, Lukáš, Lasabová, Zora

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Congenital hypofibrinogenemia associated with a novel heterozygous nonsense mutation in the globular C-terminal domain of the γ-chain (p.Glu275Stop) von Simurda, Tomas, Caccia, Sonia, Asselta, Rosanna, Zolkova, Jana, Stasko, Jan, Skornova, Ingrid, Snahnicanova, Zuzana, Loderer, Dusan, Lasabova, Zora, Kubisz, Peter

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Identification of Two Novel Fibrinogen Bβ Chain Mutations in Two Slovak Families with Quantitative Fibrinogen Disorders von Simurda, Tomas, Zolkova, Jana, Snahnicanova, Zuzana, Loderer, Dusan, Skornova, Ingrid, Sokol, Juraj, Hudecek, Jan, Stasko, Jan, Lasabova, Zora, Kubisz, Peter

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Genetic and epigenetic analysis of the beta-2-microglobulin gene in microsatellite instable colorectal cancer von Snahnicanova, Zuzana, Kasubova, Ivana, Kalman, Michal, Grendar, Marian, Mikolajcik, Peter, Gabonova, Eva, Laca, Ludovit, Caprnda, Martin, Rodrigo, Luis, Ciccocioppo, Rachele, Kruzliak, Peter, Plank, Lukas, Lasabova, Zora

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Assessment of Antioxidative, Chelating, and DNA-Protective Effects of Selected Essential Oil Components (Eugenol, Carvacrol, Thymol, Borneol, Eucalyptol) of Plants and Intact Rosma... von Horvathova, Eva, Navarova, Jana, Galova, Eliska, Sevcovicova, Andrea, Chodakova, Lenka, Snahnicanova, Zuzana, Melusova, Martina, Kozics, Katarina, Slamenova, Darina

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Short-term metabolic control and sleep in children and adolescents with type 1 diabetes mellitus von Kostkova, Martina, Durdik, Peter, Ciljakova, Miriam, Vojtkova, Jarmila, Sujanska, Anna, Pozorciakova, Katarina, Snahnicanova, Zuzana, Jancinova, Maria, Banovcin, Peter

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The Role of CADM1 and MAL Promoter Methylation in Inflammation and Cervical Intraepithelial Neoplasia von Holubekova, Veronika, Mersakova, Sandra, Grendar, Marian, Snahnicanova, Zuzana, Kudela, Erik, Kalman, Michal, Lasabova, Zora, Danko, Jan, Zubor, Pavol

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Association between 3'UTR polymorphisms in genes ACVR2A, AGTR1 and RGS2 and preeclampsia von Mendelova, Andrea, Holubekova, Veronika, Grendar, Marian, Zubor, Pavol, Svecova, Iveta, Loderer, Dusan, Snahnicanova, Zuzana, Biringer, Kamil, Danko, Jan, Lasabova, Zora

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Association of Polymorphisms in CYBA, SOD1, and CAT Genes with Type 1 Diabetes and Diabetic Peripheral Neuropathy in Children and Adolescents von Snahnicanova, Zuzana, Mendelova, Andrea, Grendar, Marian, Holubekova, Veronika, Kostkova, Martina, Pozorciakova, Katarina, Jancinová, Maria, Kasubova, Ivana, Vojtkova, Jarmila, Durdik, Peter, Lasabova, Zora, Ciljakova, Miriam, Banovcin, Peter

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Congenital hypofibrinogenemia associated with a novel heterozygous nonsense mutation in the globular C-terminal domain of the γ-chain (p.Glu275Stop) von Simurda, Tomas, Caccia, Sonia, Asselta, Rosanna, Zolkova, Jana, Stasko, Jan, Skornova, Ingrid, Snahnicanova, Zuzana, Loderer, Dusan, Lasabova, Zora, Kubisz, Peter

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