Local thrombolysis for deep vein thrombosis: why, for whom and how? von Radvan, Martin, Hustý, Jakub, Floriánová, Alena, Hořáková, Kateřina, Kala, Petr

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Mutation analysis of ion channel genes promoters in ventricular fibrillation survivors with coronary artery disease von Novotny, Tomas, Raudenska, Martina, Kadlecova, Jitka, Andrsova, Irena, Florianova, Alena, Vasku, Anna, Kozak, Milan, Sepsi, Milan, Krivan, Lubomir, Gaillyova, Renata, Spinar, Jindrich

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Clinical characteristics of 30 Czech families with long QT syndrome and KCNQ1 and KCNH2 gene mutations: importance of exercise testing von Andrsova, Irena, MD, Novotny, Tomas, MD, PhD, Kadlecova, Jitka, DrS, PhD, Bittnerova, Alexandra, MA, Vit, Pavel, MD, PhD, Florianova, Alena, MD, Sisakova, Martina, MD, Gaillyova, Renata, MD, PhD, Manouskova, Lenka, RN, Spinar, Jindrich, MD, PhD

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Clinical characteristics of three Czech families with catecholaminergic polymorphic ventricular tachycardia and pilot results of RyR2 gene mutation analysis von Novotný, Tomáš, Kubuš, Peter, Vít, Pavel, Floriánová, Alena, Dohnalová, Irena, Valášková, Iveta, Kadlecová, Jitka, Gaillyová, Renata, Švandová, Eva, Špinar, Jindřich

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Mutation Analysis Ion Channel Genes Ventricular Fibrillation Survivors with Coronary Artery Disease von NOVOTNY, TOMAS, KADLECOVA, JITKA, RAUDENSKA, MARTINA, BITTNEROVA, ALEXANDRA, ANDRSOVA, IRENA, FLORIANOVA, ALENA, VASKU, ANNA, NEUGEBAUER, PETR, KOZAK, MILAN, SEPSI, MILAN, KRIVAN, LUBOMIR, GAILLYOVA, RENATA, SPINAR, JINDRICH

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Monitoring of QT interval in patients treated with psychotropic drugs von Novotny, Tomas, Florianova, Alena, Ceskova, Eva, Weislamplova, Marcela, Palensky, Vitezslav, Tomanova, Jana, Sisakova, Martina, Toman, Ondrej, Spinar, Jindrich

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The Homozygous KCNQ1 Gene Mutation Associated with Recessive Romano–Ward Syndrome von NOVOTNY, TOMAS, KADLECOVA, JITKA, JANOUSEK, JAN, GAILLYOVA, RENATA, BITTNEROVA, ALEXANDRA, FLORIANOVA, ALENA, SISAKOVA, MARTINA, TOMAN, ONDREJ, CHROUST, KAREL, PAPOUSEK, IVO, SPINAR, JINDRICH

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Occurrence of notched T wave in healthy family members with the long QT interval syndrome von Novotny, Tomas, Sisakova, Martina, Kadlecova, Jitka, Florianova, Alena, Semrad, Borivoj, Gaillyova, Renata, Vlasinova, Jitka, Chroust, Karel, Toman, Ondrej

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CASE REPORTS: The Homozygous KCNQ1 Gene Mutation Associated with Recessive Romano-Ward Syndrome von Novotny, Tomas, Kadlecova, Jitka, Janousek, Jan, Gaillyova, Renata, Bittnerova, Alexandra, Florianova, Alena, Sisakova, Martina, Toman, Ondrej, Chroust, Karel, Papousek, Ivo, Spinar, Jindrich

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The Homozygous KCNQ1 Gene Mutation Associated with Recessive Romano-Ward Syndrome von NOVOTNY, TOMAS, KADLECOVA, JITKA, JANOUSEK, JAN, GAILLYOVA, RENATA, BITTNEROVA, ALEXANDRA, FLORIANOVA, ALENA, SISAKOVA, MARTINA, TOMAN, ONDREJ, CHROUST, KAREL, PAPOUSEK, IVO, SPINAR, JINDRICH

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