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Publications by E. Klaskova
EP04.36: Fetal Sinus Bradycardia as the Symptom of Previously Undiagnosed Familial Form of Long QT Syndrome Type 1 Caused by Mutation of KCNQ1 Gene (C.926C>T)
Ultrasound in Obstetrics and Gynecology
Nuclear Medicine
Radiology
Ultrasound Technology
Gynecology
Reproductive Medicine
Radiological
Imaging
Obstetrics
Medicine
EP21.01: Management of Pregnancies at Risk of Hemolytic Disease of the Fetus and Newborn in the Czech Republic
Ultrasound in Obstetrics and Gynecology
Nuclear Medicine
Radiology
Ultrasound Technology
Gynecology
Reproductive Medicine
Radiological
Imaging
Obstetrics
Medicine
Related publications
R231C Mutation in KCNQ1 Causes Long QT Syndrome Type 1 and Familial Atrial Fibrillation
Heart Rhythm
Cardiovascular Medicine
Physiology
Cardiology
Clinical and Electrophysiological Characterization of a Novel Mutation (F193L) in the KCNQ1 Gene Associated With Long QT Syndrome
Clinical Science
Medicine
Gillespiе Syndrome, Caused by Previously Undescribed Mutation in the Gene ITPR1
Russkii Zhunal Detskoi Nevrologii
Child Health
Neurology
Pediatrics
Perinatology
Familial Long QT Syndrome
Long QT Syndrome With Nocturnal Cardiac Events Caused by a KCNH2 Missense Mutation (G604S)
Internal Medicine
Internal Medicine
Medicine
Familial Long QT Syndrome Presented as Ventricular Tachycardia During Anesthesia
Paediatric Anaesthesia
Child Health
Pediatrics
Anesthesiology
Pain Medicine
Perinatology
Congenital Long-Qt Syndrome Caused by a Novel Mutation in a Conserved Acidic Domain of the Cardiac Na+ Channel
Circulation
Cardiovascular Medicine
Physiology
Cardiology
Identification of a Novel KCNQ1 Frameshift Mutation and Review of the Literature Among Iranian Long QT Families
Iranian Biomedical Journal
Biochemistry
Clinical Biochemistry
Genetics
Molecular Biology
Impaired KCNQ1-KCNE1 and Phosphatidylinositol-4,5-Bisphosphate Interaction Underlies the Long QT Syndrome
Circulation Research
Cardiovascular Medicine
Physiology
Cardiology
