MUDr. Renata Gaillyová, Ph.D.
Section of Genetics and Molecular Biology
Phone: | +420 532 23 4489 |
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E‑mail: |
Total number of publications: 194
2002
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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
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The occurence of notched T waves in healthy members of LQT families
Europace, year: 2002, edition: 3(suppl.A)
2001
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Use of New Modified PCR-based Methods for Rapid Differential Diagnostics of Myotonic Dystrophy.
Year: 2001, type: Conference abstract
2000
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Cirkadiánní kolísání hodnot QT intervalu pacientů se syndromem dlouhého QT
Sborník abstrakt č. 5, year: 2000
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Exercise testing reveals individuals with an asymptomatic long QT syndrome
Book of abstracts, year: 2000
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Interfamiliární rozdíly zátěžového chování QT intervalu v rodinách se syndromem dlouhého QT
Sborník abstrakt, year: 2000
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Intermitentní normální hodnoty QT intervalu u pacientů s průkazem mutace KCNQ1 genu
Sborník abstrakt, year: 2000
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Methodological Possibilities for detection of expanded trinucleotide repeats in myotonic dystrophy locus.
Year: 2000, type: Conference abstract