Total number of publications: 201
2004
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Spectrum of mutation and single-nucleotide polymorphism in long QT syndrome genes KCNQ1, KCNH2 and KCNE1.
Eur J Hum Genet, year: 2004, volume: 12, edition: suppl. 1
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Variabilita klinických projevů u pacientů s geneticky potvrzenou diagnózou syndromu dlouhého QT
Cor et Vasa, year: 2004, volume: 46, edition: S4
2003
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Genetika dystonií
Česká a slovenská neurologie a neurochirurgie, year: 2003, volume: 66/99, edition: 5
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Molecular genetics of the long QT syndrome: screening for mutations in the genes KvLQT1, HERG and KCNE1 in Czech long QT families.
Eur J Hum Genet, year: 2003, edition: 11 suppl.1
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Mutation detection in KCNE1 gene encoding cardiac channel subunit: first experience with using of SSCP analysis by capillary electrophoresis for maximize detection effiency.
Eur J Hum Genet, year: 2003, edition: 11 suppl.1
2002
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Comparison of different formulas of QT interval correction in LQT families during exercise.
Book of Abstracts, 10th Alpe Adria Cardiology Meeting, year: 2002
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Identifikace nové mutace genu KCNQ1 v české rodině s fenotypem LQT
Cor et Vasa, year: 2002, volume: 44, edition: suppl.
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Mutational analyses of potassium channel gene KVLQT1 and identification of a novel long-QT syndrome mutation (T309I)
Eur J Hum Genet, year: 2002, edition: 10 suppl.1
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New mutation in the KCNQ1 gene identified in a Czech family with LQT phenotype.
Book of Abstracts 10th Alpe Adria Cardiology Meeting, year: 2002
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Srovnání různých metod korekce QT intervalu při zátěži v LQT rodinách
Cor et Vasa, year: 2002, volume: 44, edition: suppl