MUDr. Renata Gaillyová, Ph.D.
Institute of Medical Genetics and Genomics
phone: | +420 532 23 4489 |
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e‑mail: |
Total number of publications: 197
2003
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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
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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