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Tomoya Kaneda
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Articles

A novel β-myosin heavy chain gene mutation, p.Met531Arg, identified in isolated left ventricular non-compaction in humans, results in left ventricular hypertrophy that progresses to dilation in a mouse model

Tomoya Kaneda, Chie Naruse, Atsuhiro Kawashima, Noboru Fujino, Toru Oshima, Masanobu Namura, Shinichi Nunoda, Sumio Mori, Tetsuo Konno, Hidekazu Ino, Masakazu Yamagishi, Masahide Asano
Journal: Clinical Science
Clin Sci (Lond) (2008) 114 (6): 431–440.
https://doi.org/10.1042/CS20070179
Published: 12 February 2008
View article titled, A novel β-myosin heavy chain gene mutation, p.Met531Arg, identified in isolated left ventricular non-compaction in humans, results in left ventricular hypertrophy that progresses to dilation in a mouse model
Open the PDF for A novel β-myosin heavy chain gene mutation, p.Met531Arg, identified in isolated left ventricular non-compaction in humans, results in left ventricular hypertrophy that progresses to dilation in a mouse model in another window
Articles

A novel mutation in the cardiac myosin-binding protein C gene is responsible for hypertrophic cardiomyopathy with severe ventricular hypertrophy and sudden death

Tetsuo Konno, Masami Shimizu, Hidekazu Ino, Noboru Fujino, Katsuharu Uchiyama, Tomohito Mabuchi, Kenji Sakata, Tomoya Kaneda, Takashi Fujita, Eiichi Masuta, Hiroshi Mabuchi
Journal: Clinical Science
Clin Sci (Lond) (2006) 110 (1): 125–131.
https://doi.org/10.1042/CS20050189
Published: 12 December 2005
View article titled, A novel mutation in the cardiac myosin-binding protein C gene is responsible for hypertrophic cardiomyopathy with severe ventricular hypertrophy and sudden death
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Articles

Compound heterozygosity for mutations Asp 611 →Tyr in KCNQ1 and Asp 609 →Gly in KCNH2 associated with severe long QT syndrome

Masato YAMAGUCHI, Masami SHIMIZU, Hidekazu INO, Hidenobu TERAI, Kenshi HAYASHI, Tomoya KANEDA, Hiroshi MABUCHI, Ryo SUMITA, Tohru OSHIMA, Naoto HOSHI, Haruhiro HIGASHIDA
Journal: Clinical Science
Clin Sci (Lond) (2005) 108 (2): 143–150.
https://doi.org/10.1042/CS20040220
Published: 21 January 2005
View article titled, Compound heterozygosity for mutations Asp 611 →Tyr in KCNQ1 and Asp 609 →Gly in KCNH2 associated with severe long QT syndrome
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Articles

T wave peak-to-end interval and QT dispersion in acquired long QT syndrome: a new index for arrhythmogenicity

Masato YAMAGUCHI, Masami SHIMIZU, Hidekazu INO, Hidenobu TERAI, Katsuharu UCHIYAMA, Kotaro OE, Tomohito MABUCHI, Tetsuo KONNO, Tomoya KANEDA, Hiroshi MABUCHI
Journal: Clinical Science
Clin Sci (Lond) (2003) 105 (6): 671–676.
https://doi.org/10.1042/CS20030010
Published: 01 December 2003
View article titled, T wave peak-to-end interval and QT dispersion in acquired long QT syndrome: a new index for arrhythmogenicity
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