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Circulation Journal : Official Journal of the Japanese Circulation Society|April 2, 2009
Phenotypic overlap of cardiac sodium channelopathies: individual-specific or mutation-specific?Naomasa MakitaCurrent Opinion in Cardiology|March 3, 2012
Cardiac connexins, mutations and arrhythmiasMario Delmar, Naomasa MakitaCirculation Journal : Official Journal of the Japanese Circulation Society|December 6, 2007
Genetic polymorphisms and arrhythmia susceptibilityNaomasa Makita, Hiroyuki TsutsuiCirculation Journal : Official Journal of the Japanese Circulation Society|May 27, 2008
Absence of a trafficking defect in R1232W/T1620M, a double SCN5A mutant responsible for Brugada syndromeNaomasa Makita, Naoki Mochizuki, Hiroyuki TsutsuiJournal of Arrhythmia|October 21, 2016
Inherited bradyarrhythmia: A diverse genetic backgroundTaisuke Ishikawa, Yukiomi Tsuji, Naomasa MakitaHeart Rhythm|April 3, 2007
Novel SCN5A mutation (Q55X) associated with age-dependent expression of Brugada syndrome presenting as neurally mediated syncopeNaomasa Makita, Naokata Sumitomo, Ichiro Watanabe, et al.Pediatrics International : Official Journal of the Japan Pediatric Society|May 26, 2020
Dynamic QT response to cold-water face immersion in long-QT syndrome type 3Kazuhiro Takahashi, Wataru Shimizu, Naomasa Makita, et al.Journal of Pediatric Genetics|October 21, 2022
A Case Report: Two Young Children with Long QT Syndrome Type-2 Diagnosed by Presymptomatic Genetic TestingYuki Matsushita, Hazumu Nagata, Masanobu Ogawa, et al.Cardiovascular Research|December 29, 2004
Intrinsic mechanism of the enhanced rate-dependent QT shortening in the R1623Q mutant of the LQT3 syndromeYasushi Oginosawa, Toshihisa Nagatomo, Haruhiko Abe, et al.Human Genome Variation|August 8, 2022
Arrhythmogenic right ventricular cardiomyopathy in a Japanese patient with a homozygous founder variant of DSG2 in the East Asian populationHaruka Murakami, Yoko Tanimoto, Kojiro Tanimoto, et al.Pageof 10