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Publications by Haruhiro HIGASHIDA
Clinical and Electrophysiological Characterization of a Novel Mutation (F193L) in the KCNQ1 Gene Associated With Long QT Syndrome
Clinical Science
Medicine
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R231C Mutation in KCNQ1 Causes Long QT Syndrome Type 1 and Familial Atrial Fibrillation
Heart Rhythm
Cardiovascular Medicine
Physiology
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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
Clinical, Genetic, and Biophysical Characterization of a Homozygous HERG Mutation Causing Severe Neonatal Long QT Syndrome
Pediatric Research
Child Health
Pediatrics
Perinatology
Overlapping LQT1 and LQT2 Phenotype in a Patient With Long QT Syndrome Associated With Loss-Of-Function Variations in KCNQ1 and KCNH2
Biophysical Journal
Biophysics
Impaired KCNQ1-KCNE1 and Phosphatidylinositol-4,5-Bisphosphate Interaction Underlies the Long QT Syndrome
Circulation Research
Cardiovascular Medicine
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Novel Arrhythmogenic Mechanism Revealed by a Long-Qt Syndrome Mutation in the Cardiac Na+ Channel
Circulation Research
Cardiovascular Medicine
Physiology
Cardiology
A Novel ROGDI Gene Mutation Is Associated With Kohlschutter-Tonz Syndrome
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology
Nuclear Medicine
Radiology
Oral Surgery
Imaging
Dentistry
Forensic Medicine
Pathology
Surgery
Novel Deletion Mutation in the Cardiac Sodium Channel Inactivation Gate Causes Long QT Syndrome
International Journal of Cardiology
Cardiovascular Medicine
Cardiology
Ion Channel Mechanisms Related to Sudden Cardiac Death in Phenotype-Negative Long-Qt Syndrome Genotype-Phenotype Correlations of the KCNQ1(S349W) Mutation
Journal of Cardiovascular Electrophysiology
Cardiovascular Medicine
Physiology
Cardiology
