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Tetsuo Konno
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Articles

Long QT syndrome and associated gene mutation carriers in Japanese children: results from ECG screening examinations

Kenshi Hayashi, Noboru Fujino, Katsuharu Uchiyama, Hidekazu Ino, Kenji Sakata, Tetsuo Konno, Eiichi Masuta, Akira Funada, Yuichiro Sakamoto, Toshinari Tsubokawa, Keisuke Nakashima, Li Liu, Haruhiro Higashida, Yoshitake Hiramaru, Masami Shimizu, Masakazu Yamagishi
Journal: Clinical Science
Clin Sci (Lond) (2009) 117 (12): 415–424.
https://doi.org/10.1042/CS20080528
Published: 21 September 2009
View article titled, Long QT syndrome and associated gene mutation carriers in Japanese children: results from ECG screening examinations
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Articles

Expression and function of ephrin-B1 and its cognate receptor EphB2 in human atherosclerosis: from an aspect of chemotaxis

Aiji Sakamoto, Hatsue Ishibashi-Ueda, Yuka Sugamoto, Takeo Higashikata, Susumu Miyamoto, Masa-aki Kawashiri, Kunimasa Yagi, Tetsuo Konno, Kenshi Hayashi, Noboru Fujino, Hidekazu Ino, Yoshiyu Takeda, Masakazu Yamagishi
Journal: Clinical Science
Clin Sci (Lond) (2008) 114 (10): 643–650.
https://doi.org/10.1042/CS20070339
Published: 14 April 2008
View article titled, Expression and function of ephrin-B1 and its cognate receptor EphB2 in human atherosclerosis: from an aspect of chemotaxis
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Includes: Supplementary data
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
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Articles

Differences in the diagnostic value of various criteria of negative T waves for hypertrophic cardiomyopathy based on a molecular genetic diagnosis

Tetsuo Konno, Noboru Fujino, Kenshi Hayashi, Katsuharu Uchiyama, Eiichi Masuta, Hiromasa Katoh, Yuichiro Sakamoto, Toshinari Tsubokawa, Hidekazu Ino, Masakazu Yamagishi
Journal: Clinical Science
Clin Sci (Lond) (2007) 112 (11): 577–582.
https://doi.org/10.1042/CS20060293
Published: 01 May 2007
View article titled, Differences in the diagnostic value of various criteria of negative T waves for hypertrophic cardiomyopathy based on a molecular genetic diagnosis
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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

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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