Mabuchi Hiroshi | Molecular Genetics Of Cardiovascular Disorders Division Of Cardiovascular Medicine Graduate School O
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概要
- Hiroe Michiakiの詳細を見る
- 同名の論文著者
- Molecular Genetics Of Cardiovascular Disorders Division Of Cardiovascular Medicine Graduate School Oの論文著者
関連著者
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Mabuchi Hiroshi
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Shimizu Masami
Molecular Genetics Of Cardiovascular Disorders Division Of Cardiovascular Medicine Graduate School O
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Shimizu Masami
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Ino Hidekazu
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Yamaguchi Masato
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Terai Hidenobu
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Mizuno Sumio
福井心臓血圧センター
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Mizuno Sumio
金沢大学 循環器内科
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Sakata Kenji
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Kaneda Tomoya
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Kaneda Tomoya
Molecular Genetics Of Cardiovascular Disorders Division Of Cardiovascular Medicine Graduate School O
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Sakata Kenji
金沢大学 医学系研究科循環器内科学
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Hayashi Kenshi
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Inoue Masaru
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Inoue Masaru
Division Of Cardiology Ishikawa Prefectural Hospital
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Konno Tetsuo
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Shimizu Masami
Cardiovascular Checkup Committee For School Pupils Of Kanazawa Medical Association
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Mabuchi Tomohito
Department of Cardiology, Fukui Prefectural Hospital
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Mabuchi Tomohito
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Mabuchi Tomohito
Department Of Cardiology Fukui Prefectural Hospital
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Ohosato Kazuo
Fukui Cardiovascular Center
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Fujino Noboru
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Uchiyama Katsuharu
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Terai Hidenobu
Division Of Cardiology Kanazawa Cardiovascular Hospital
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Uchiyama Katsuharu
Division Of Cardiovascular Medicine Kanazawa University Graduate School Of Medical Science
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Kiyama Masaru
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Hayashi Tatsumi
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Terai Hidenobu
Division of Cardiology, Kanazawa Cardiovascular Hospital
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Inoue Masaru
Department Of Cardiology Ishikawa Prefectural Central Hospital
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Mabuchi H
Kanazawa Univ. School Of Medicine Kanazawa Jpn
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HIGASHIKATA Toshinori
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Higashikata Toshinori
Molecular Genetics Of Cardiovascular Disorders Division Of Cardiovascular Medicine Graduate School O
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Inazu Akihiro
Molecular Biochemistry And Molecular Biology Laboratory Kanazawa University Graduate School Of Medic
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Mabuchi Hiroshi
Departments Of Lipidology Kanazawa University Graduate School Of Medical Science
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Higashida Haruhiro
Department Of Biophysical Genetics Kanazawa University Graduate School Of Medical Science
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Higashida Haruhiro
Biophysical Genetics, Division of Neuroscience, Kanazawa University Graduate School of Medical Scien
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NOHARA Atsushi
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine (The Second Depa
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Yamaguchi Masato
Division Of Cardiovascular Medicine Kanazawa University Graduate School Of Medical Science
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Shimizu Masami
金沢大学 循環器内科
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Mabuchi H
Departments Of Lipidology Kanazawa University Graduate School Of Medical Science
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Kitamura Masaru
Department Of Radiology Kanazawa Cardiovascular Hospital
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Konno Tetsuo
Division Of Cardiovascular Medicine Kanazawa University Graduate School Of Medicine
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Kanaya Honin
Division Of Cardiology Ishikawa Prefectural Hospital
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Kanaya Hounin
石川県立中央病院 循環器内科
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Honin Kanaya
石川県立中央病院
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Nohara Atsushi
Departments Of Lipidology Kanazawa University Graduate School Of Medical Science
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Koizumi Junji
金沢大学 医学系研究科循環医科学専攻臓器機能制御学
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Kurumaya Hiroshi
石川県立中央病院 循環器内科
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Oe Kotaro
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Nagata Mitsuru
Division Of Cardiology Kanazawa University
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Noji Yoshihiro
Department Of Internal Medicine And Molecular Genetics Of Cardiovascular Disorders Division Of Cardi
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Hayashi Kenshi
Division Of Cardiovascular Medicine Kanazawa University Graduate School Of Medical Science
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Taki Junichi
Biotracer Medicine, Division of Cancer Medicine, Graduate School of Medical Science, Kanazawa Univer
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Taki Junichi
Department Of Nuclear Medicine Kanazawa University
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Hifumi Senshu
Department Of Internal Medicine Hokuriku Central Hospital
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Takamura Masayuki
Department Of Cardiology Kanazawa University
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Fujita Takashi
Department Of Cardiology Kanazawa University
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KAKU Bunji
Division of Cardiology, Ishikawa Prefectural Hospital
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KANAYA Hounin
Division of Cardiology, Ishikawa Prefectural Hospital
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NOJI Yoshihiro
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine (The Second Depa
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Kawashiri Masaaki
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Disease
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Hifumi Senshu
Division Of Internal Medicine Hokuriku Central Hospital
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Kaku Bunji
Division Of Cardiology Ishikawa Prefectural Hospital
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Kaku Bunji
福井県循環器病院
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Taki Junichi
Kanazawa University Hospital
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滝 淳一
金沢大学 大学院医学研究科整形外科
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Itoh Hideki
Department Of Cardiovascular And Respiratory Medicine Shiga University Of Medical Science
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Fujita Takashi
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Kanazawa Univer
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Takata Hiroyuki
金沢大学 医学系研究科血管分子遺伝学
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Kobayashi Junji
Department of Lipidology, Kanazawa University Graduate School of Medical Science
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Koizumi Junji
Department of General Medicine, Kanazawa University Hospital
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Yagi Kunimasa
Department of Internal Medicine, Kanazawa University Graduate School of Medical Science
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Takata Hiroyuki
Molecular Genetics Of Cardiovascular Disorders Graduate School Of Medical Science Kanazawa Universit
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Yagi Kunimasa
金沢大学 医学系研究科循環医科学専攻臓器機能制御学
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Yagi Kunimasa
Department Of Internal Medicine Kanazawa University Graduate School Of Medical Science
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Yagi Kunimasa
Department Of Internal Medicine Kanazawa University Hospital
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Hoshi Naoto
Biophysical Genetics Division Of Neuroscience Graduate School Of Medical Science Kanazawa University
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Taki Junichi
先端医学薬学研究センター
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HIFUMI Senshu
Department of Internal Medicine, Hokuriku Central Hospital
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Uno Yoshihide
Department of Cardiology, Ishikawa Prefectural Central Hospital
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Takeda Yoshiyu
Molecular Genetics Of Cardiovascular Disorders Graduate School Of Medical Science Kanazawa Universit
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Takeda Yoshiyu
Division Of Endocrinology And Hypertension Kanazawa University Graduate School Of Medicine
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Funada Akira
Division Of Cardiovascular Medicine Kanazawa University Graduate School Of Medical Science
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Takata Mutsuko
Division Of Cardiovascular Medicine Kanazawa University Graduate School Of Medical Science
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Koizumi Junji
Departments Of Lipidology Kanazawa University Graduate School Of Medical Science
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Uno Yoshihide
Department Of Cardiology Ishikawa Prefectural Central Hospital
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Miwa Kenji
Division Of Cardiology Ishikawa Prefectural Hospital
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Matsuyama Toru
Molecular Genetics Of Cardiovascular Disorders Division Of Cardiovascular Medicine Graduate School O
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Ino Hidekazu
金沢大学 医学系研究科循環器内科
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YAGI Kunimasa
Molecular Genetics of Cardiovascular Disorders, Graduate School of Medical Science, Kanazawa Univers
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OHKA Takio
Division of Cardiology, Ishikawa Prefectural Hospital
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Funada Akira
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Inazu Akihiro
School of Health Sciences, Faculty of Medicine, Kanazawa University
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YU Wenxin
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine (The Second Depa
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Takata Mutsuko
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Disease
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Miwa Kenji
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Disease
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Yu W
Department Of Internal Medicine And Molecular Genetics Of Cardiovascular Disorders Division Of Cardi
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Yu Wenxin
金沢大学 医学系研究科血管分子遺伝学
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Uedsa Kousei
Division Of Cardiology Komatsu Municipal Hospital
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Ueda Kosei
Komatsu Municipal Hospital
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Katsuda Shoji
Division Of Cardiology Graduate School Of Medical Science Kanazawa University
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Takeda Yoshiyu
Department Of Internal Medicine Graduate School Of Medical Science Kanazawa University
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Umeda Ken
Second Department Of Internal Medicine School Of Medicine Kanazawa University
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Koizumi Junji
Department Of General Medicine Kanazawa University Graduate School Of Medical Science
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Yagi Kunimasa
Division Of Cardiovascular Medicine Kanazawa University Graduate School Of Medicine
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Yagi Kunimasa
Molecular Genetics Of Cardiovascular Disorders Graduate School Of Medical Science Kanazawa Universit
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Namura Masanobu
Kanazawa Cardiovascular Hospital
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野中 聡
旭川医科大学耳鼻咽喉科・頭頸部外科学講座
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野中 源一郎
九州大学薬学部
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ORIGASA Hideki
Division of Biostatistics and Clinical Epidemiology, University of Toyama School of Medicine
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中嶋 憲一
Kanazawa Univ. Kanazawa Jpn
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中嶋 憲一
金沢大学 医学部附属病院 核医学診療科
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Nagasawa Shinya
Department of Health Science, Shiga University of Medical Science
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SAKATA Kenji
Division of Cardiovascular Medicine, Kanazawa University Graduate School of Medicine
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Nakajima Kenichi
Kanazawa Univ. Hospital Kanazawa Jpn
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Shimizu Kuniyoshi
The Second Department Of Internal Medicine School Of Medicine Kanazawa University
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Shimizu Kuniyoshi
Department Of Forest And Forest Products Sciences Faculty Of Agriculture Kyushu University
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Suehiro Tadashi
Second Department Of Internal Medicine Kochi Medical School
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Namura Masanobu
Department of Cardiology, Kanazawa Cardiovascular Hospital
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Nakajima Kenichi
Biotracer Medicine, Division of Cancer Medicine, Graduate School of Medical Science, Kanazawa Univer
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Kawano Masaya
Biotracer Medicine, Kanazawa University
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Origasa Hideki
Division Of Biostatistics Toyama Medical And Pharmaceutical University
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Mizuno Sumio
Department Of Cardiology Fukui Cardiovascular Center
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Shimizu Kuniyoshi
Department Of Internal Medicine Kouseiren Takaoka Hospital
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Kobayashi Tsutomu
Department of Hypertension and Cardiorenal Medicine, Dokkyo University School of Medicine
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Nohara Atsushi
Department of Lipidology, Kanazawa University Graduate School of Medical Science
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Inoue Masaru
石川県立中央病院 循環器内科
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Katoh Masahiko
日本大学医学部附属駿河台病院 循環器科
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Miwa Kenji
Department of Cardiology, Ishikawa Prefectural Central Hospital
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Kanaya Honin
Division of Cardiovascular Medicine, Kanazawa University Graduate School of Medicine
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MURAMOTO Hiroaki
Kanazawa Social Insurance Hospital
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NOZUE Tsuyoshi
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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KAWASHIRI Masa-aki
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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MURASE Yuko
Department of Lifestyle-related disease, Kanazawa University Graduate School of Medical Science
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INAZU Akihiro
Kanazawa University, Faculty of Medicine, School of Health Science, Laboratory Sciences
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Murase Yuko
Department Of Lifestyle-related Disease Kanazawa University Graduate School Of Medical Science
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Murase Yuko
Molecular Genetics Of Cardiovascular Disorders Graduate School Of Medical Science Kanazawa Universit
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Nozue Tsuyoshi
Department Of Internal Medicine Yokohama Sakae Kyosai Hospital
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Masuta Eiichi
Division Of Cardiovascular Medicine Kanazawa University Graduate School Of Medical Science
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Mizuno Sumio
Fukui Cardiovascular Center
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Hifumi Senshu
Division of Cardiology, Kanazawa Cardiovascular Hospital
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Mizuno Kiyo-o
Division of Internal Medicine, Fukui Cardiovascular Hospital
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Sakata Kenji
Division Of Cardiovascular Medicine Kanazawa University Graduate School Of Medicine
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Yasuda Toshihiko
Division Of Cardiology Ishikawa Prefectural Hospital
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Yasuda Toshihiko
Ishikawa Prefectural Central Hospital
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Uno Yoshihide
Division Of Cardiology Ishikawa Prefectural Hospital
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Uno Yoshihide
Department Of Applied Physics Faculty Of Engineering Fukui University
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Matsubara Takao
Department Of Cardiology Ishikawa Prefectural Central Hospital
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中嶋 憲一
金沢大学医学部附核医学教室
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SUGIHARA Masako
Department of Internal Medicine, Kanazawa Social Insurance Hospital
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CHUJO Daisuke
Molecular Genetics of Cardiovascular Disorders, Graduate School of Medical Science, Kanazawa Univers
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OTSUJI Michio
Molecular Genetics of Cardiovascular Disorders, Graduate School of Medical Science, Kanazawa Univers
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MURAMOTO Hiroaki
Department of Internal Medicine, Kanazawa Social Insurance Hospital
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HORITA Yuki
Division of Cardiology, Ishikawa Prefectural Hospital
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YAMAZAKI Tsukasa
Division of Cardiology, Ishikawa Prefectural Hospital
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Tatami Ryozo
Division of Cardiology, Maizuru Kyousai Hospital
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Ishise Syozo
Division of Cardiology, Maizuru Kyousai Hospital
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Fujita Takashi
Division of Cardiology, Department of Internal Medicine, Ishikawa Prefectural Central Hospital
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Ueda Mikio
Divisions of Hematology, Ishikawa Prefectural Hospital
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Seki Masahiro
Divisions of Cardiovascular Surgery, Ishikawa Prefectural Hospital
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Misawa Katsushi
Department of Internal Medicine, Himi Municipal Hospital
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Michishita Ichiro
Department of Internal Medicine, Yokohama Sakae Kyosai Hospital
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Genda Akira
Department of Internal Medicine, Yokohama Sakae Kyousai Hospital
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Nitta Yutaka
Department of Cardiology, Toyama Red Cross Hospital
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TODO Yasuhiro
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine (The Second Depa
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Otsuji Michio
Molecular Genetics Of Cardiovascular Disorders Graduate School Of Medical Science Kanazawa Universit
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Katsuda Shoji
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Disease
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Kawashiri Masaaki
Kanazawa University, School of Health Science, Faculty of Medicine
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Yasuda Toshihiko
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Masuta Eiichi
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Katoh Masahiro
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Noji Yoshihiro
Department Of Cardiology Fukui Prefectural Hospital
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Todo Yasuhiro
Molecular Genetics Of Cardiovascular Disorders Division Of Cardiovascular Medicine (the Second Depar
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Tatami Ryozo
Division Of Cardiology Maizuru Kyousai Hospital
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Fujii Hiroyuki
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Michishita Ichiro
Department Of Internal Medicine Yokohama Sakae Kyosai Hospital
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Yoshida Koujiro
Toyama Municipal Hospital
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GUO Zhigang
Molecular Genetics of Cardiovascular Disorders, Vascular Medicine, Division of Cardiovascular Medici
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SUZUMURA Takeo
Department of Laboratory Science, School of Health Sciences, Kanazawa University
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OKAMOTO Michiko
Department of Laboratory Science, School of Health Sciences, Kanazawa University
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SANO Ryuichi
Sano Clinic
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WAKASUGI Kazuyoshi
Wakasugi Clinic
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HAYAKAWA Tetsuo
Toyama Municipal Hospital
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SCHMITZ Gerd
Institute for Clinical Chemistry and Laboratory Medicine, University of Regensburg
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Tsuchida Masayuki
Division Of Cardiovascular Medicine Kanazawa University Graduate School Of Medical Science
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Kawashiri Masa-aki
Division Of Cardiovascular Medicine Kanazawa University Graduate School Of Medicine
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Kasuga Tetsuya
Department of Cardiology, Kanazawa Medical University
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Sakazume Shinobu
Division of Pediatrics, NHO Kanazawa Medical Center
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Guo Zhigang
Molecular Genetics Of Cardiovascular Disorders Vascular Medicine Division Of Cardiovascular Medicine
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Schmitz Gerd
Institute For Clinical Chemistry And Laboratory Medicine University Of Regensburg
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Chujo Daisuke
Department Of Internal Medicine Kanazawa University Hospital
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Suzumura Takeo
Department Of Laboratory Science School Of Health Sciences Kanazawa University
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ITO Yuji
Department of Bioengineering, Faculty of Engineering, Kagoshima University
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Seidman Christine
Harvard Medical School
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Nohara Atushi
Molecular Genetics of Cardiovascular Disorders, Graduate School of Medical Science, Kanazawa Univers
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Kobayashi Junji
Molecular Genetics of Cardiovascular Disorders, Graduate School of Medical Science, Kanazawa Univers
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Hayashi Tatsumi
Fukui Prefectural Hospital
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Fujino Susumu
Fukui Prefectural Hospital
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Aoyama Takahiko
Fukui Prefectural Hospital
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Fujii Hiroyuki
Komatsu Municipal Hospital
著作論文
- PJ-424 Cardiac Sympathetic Nerve Activity in Patients with Hypertrophic Cardiomyopathy Caused by Thin Filament Gene Mutations(Cardiomyopathy, Clinical 5 (M) : PJ71)(Poster Session (Japanese))
- Lispro is superior to regular insulin in transient intensive insulin therapy in type 2 diabetes
- Abnormal sympathetic innervation of the heart in a patient with Emery-Dreifuss muscular dystrophy
- Differentiation between patients with takotsubo cardiomyopathy and those with anterior acute myocardial infarction
- PE-279 High Incidence of Sudden Cardiac Death with Conduction Disturbances and Atrial Cardiomyopathy Caused by a Mutation in the STA Gene(Cardiomyopathy, Clinical 3 (M) : PE48)(Poster Session (English))
- Reduction of hemolysis without reoperation following mitral valve repair
- Identification of two novel missense mutations (p.R1221C and p.R1357W) in the ABCC6 (MRP6) gene in a Japanese patient with pseudoxanthoma elasticum (PXE)
- Type III hyperlipoproteinemia exaggerated by Sheehan's syndrome with advanced systemic atherosclerosis - A 28-year clinical course
- Japan Lipid Intervention Trial (J-LIT) Chart Predicts the Absence of Coronary Artery Disease More Accurately Than Symptom Limited Exercise Stress Electrocardiography
- In-hospital Outcome in Octogenarians with Acute Coronary Syndrome Undergoing Emergent Coronary Angiography
- Gene mutations in adult Japanese patients with dilated cardiomyopathy
- Oxidative Stress Correlates with Left Ventricular Volume after Acute Myocardial Infarction
- Double deletions and missense mutations in the first nucleotide-binding fold of the ATP-binding cassette transporter A1 (ABCA1) gene in Japanese patients with Tangier disease
- Difference in the risk factors for coronary, renal and other peripheral arteriosclerosis in heterozygous familial hypercholesterolemia
- FRS-128 Mutations in Phospholamban Gene Cause Hypertrophic and Dilated Cardiomyopathy(Myocardial Disease (M) : FRS16)(Featured Research Session (English))
- Increased Circulating Matrix Metalloproteinase-2 in Patients with Hypertrophic Cardiomyopathy with Systolic Dysfunction
- Scintigraphic evaluation of regression of abnormal Q waves in myocardial infarction
- PJ-425 Early Development of Dilated Cardiomyopathy in Subjects with Mutations in the Cardiac Troponin Complex Genes(Cardiomyopathy, Clinical 5 (M) : PJ71)(Poster Session (Japanese))
- OJ-511 Missense Mutations in Cardiac Ryanodine Receptor Gene Cause Hypertrophic Cardiomyopathy Associated with Ventricular Arrhythmia or Massive Hypertrophy(Cardiomyopathy, Basic (M) : OJ62)(Oral Presentation (Japanese))
- OJ-229 Atrial Fibrillation in Patients with Hypertrophic Cardiomyopathy with Different Genotypes(Cardiomyopathy, Clinical 1 (M) : OJ26)(Oral Presentation (Japanese))
- OJ-078 Usefulness of Q-T Peak Dispersion for Diagnosis of KCNH2 Gene Mutations in Patients with Long QT Syndrome(Arrhythmia, Basic 1 (A) : OJ10)(Oral Presentation (Japanese))
- FRS-129 Mutations Responsible for Dilated Cardiomyopathy in Japan(Myocardial Disease (M) : FRS16)(Featured Research Session (English))
- PJ-596 Exercise-induced Systolic Dysfunction in Patients with Non-obstructive Hypertrophic Cardiomyopathy and Mutations in the Cardiac Troponin Genes(Cardiomyopathy, Clinical 7 (M) : PJ100)(Poster Session (Japanese))
- OJ-335 PRKAR1A Gene Mutation in Patients with Cardiac Myxoma(Valvular Heart Disease/Pericarditis/Cardiac Tumor 2 (M) : OJ40)(Oral Presentation (Japanese))
- Alterations in Echocardiographic Tissue Characterization in Patients with Cardiac Troponin I Gene Mutation a Possible Indicator of Preclinical Hypertrophic Cardiomyopathy
- Cardiac Actin and Alpha-Tropomyosin Genes Are Associated with Neither Hypertrophic Nor Dilated Cardiomyopathy in Patients from Hokuriku District in Japan
- PE-280 Missense Mutations in the MYBPC3 Gene are Responsible for Hypertrophic Cardiomyopathy with Left Ventricular Systolic Dysfunction and Dilatation(Cardiomyopathy, Clinical 3 (M) : PE48)(Poster Session (English))
- PE-278 Electrocardiography Shows Preferable Diagnostic Value Even in Carriers of Hypertrophic Cardiomyopathy who do not Manifest Ventricular Wall Hypertrophy on Echocardiography(Cardiomyopathy, Clinical 3 (M) : PE48)(Poster Session (English))
- OJ-237 KCNJ2 Gene Mutation is a Rare Cause of Long QT Syndrome(Arrhythmia, Diagnosis/Pathophysiology/EPS 9 (A) : OJ27)(Oral Presentation (Japanese))
- FRS-132 Phenotypic Discrepancies Between Electrocardiography and Echocardiography for Hypertrophic Cardiomyopathy in Genetically Affected Subjects(Myocardial Disease (M) : FRS16)(Featured Research Session (English))
- Left ventricular dysfunction and dilatation in elderly patients with hypertrophic cardiomyopathy associated with a novel missense mutation in MyBP-C gene
- Relationship between QT Variables and Disproportion of Left Ventricular Wall in Patients with Hypertrophic Cardiomyopathy
- Fluctuation of T-peak to T-end before and after ventricular tachycardia
- Q-T peak dispersion in congenital long QT syndrome ; increased lag of T wave peak as a new marker of HERG
- Pathophysiological Roles of the Adrenal Renin-Angiotensin System in Patients with Primary Aldosteronism
- Effects of Aldosterone Blockade on Cardiac Renin-Angiotensin-Aldosterone System in Salt-Sensitive Hypertension (Hypertension, Basic 5 (H), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Probucol-Induced Long QT Syndrome Associated with a Novel Missense Mutation M124T in the N Terminus of HERG
- Long QT Syndrome Mutations in Different Sites of HERG Elicit a Variety of Functional Changes
- Double Missense Mutations (D611Y in KCNQ1 and D609G in HERG) in a Japanese Family with Long QT Syndrome
- Characterization of a Novel Missense Mutation E637K in the Pore-S6 Loop of HERG in a Patient with Long QT Syndrome
- Clinical and electrophysiological characterization of a novel mutation (F193L) in the KCNQ1 gene associated with long QT syndrome
- Sixteen-slice computed tomography, transthoracic real-time 3-dimensional echocardiography and magnetic resonance imaging assessment of a long-term survivor of rupture of sinus of valsalva aneurysm
- Increased matrix metalloproteinase-2 in patients with hypertrophic cardiomyopathy with systolic dysfunction
- OJ-415 Electrocardiographic Events and Cholesterol Reduction with Pravastatin in Patients with Hypercholesterolemia : Hokuriku Lipid Coronary Heart Disease Study-Pravastatin Atherosclerosis Trial(Preventive Medicine/Epidemiology/Education 3 (H) : OJ50)(Or
- PCSK9 Gene Mutation is Less Frequent in Clinically Diagnosed FH Patients without LDLR and ApoB-100 Gene Mutation in Japan(Lipid Disorders 1 (H), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Usefulness of Acoustic Densitometry Method for Detection of Myocardial Changes in Preclinical Patients with Hypertrophic Cardiomyopathy
- Difference in Coronary Blood Flow Dynamics between Patients with Hypertension and Those with Hypertrophic Cardiomyopathy
- Q-T peak dispersion in congenital long QT syndrome: Possible marker of mutation of HERG
- Cardiac Manifestations and Long-Term Course in Emery-Dreifuss Muscular Dystrophy Caused by a Nonsense Mutation in the STA Gene
- Effects of gender on the number of diseased vessels and clinical outcome in Japanese patients with acute coronary syndrome
- A novel de novo mutation in the cardiac β - myosin heavy chain gene in patients with dilated cardiomyopathy
- Mitochondrial DNA mutations in hypertrophic cardiomyopathy
- Novel KCNQ1 missense mutation (D611Y) in a Japanese long QT family
- Whole and regional variation of cardiac sympathetic nervous activity in patients with hypertrophic cardiomyopathy with malignant tachyarrthythmias and sudden death
- Association between Single Nucleotide Polymorphisms (SNPs) of Cardiac Potassium Channel Genes and Drug-Induced Long QT Syndrome in Japanese
- A Novel Mutation (lnt21DSG+1A) in the MyBP-C Gene Shows Hypertrophic Cardiomyopathy with a High Degree of Penetrance in Adult Patients
- Diagnostic Values of Abnormal Q Waves for Hypertrophic Cardiomyopathy Based on the Genetic Information
- QT Variables in Preclinical Patients with Hypertrophic Cardiomyopathy
- QT Variables in Various Genotyped Patients with Hypertrophic Cardiomyopathy
- Mitochondrial DNA Mutations in Hypertrophic Cardiomyopathy
- Frequency of Asymmetric Septal Hypertrophy in Patients with Hypertrophic Cardiomyopathy : Difference in Genotypes
- Differences in Diagnostic Values of Abnormal Q Waves between Hypertrophic Cardiomyopathy with a cTnl Gene Mutation and MyBP-C Gene Mutations
- Clinical and Electrophysiological Characteristics of Brugada Syndrome Caused by a Missense Mutation in the S5-pore site of SCN5A(Arrhythmia, Diagnosis/Pathophysiology/EPS 5 (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- FRS-144 A Novel Missense Mutation of SCN5A Gene Associated with Brugada Syndrome by Bidirectional Effects on Blocking Actions of Antiarrhythmic Drugs(Sudden Cardiac Death (A) : FRS18)(Featured Research Session (English))
- SCN5A Gene Mutations and Clinical Characteristics in Patients With Brugada-Type Electrocardiogram