Rezultati - Horie, Minoru

Molecular genetics have opened a new era for arrhythmia research, but also Pandora׳s box? od Horie, Minoru

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Electrical disorders in atrial septal defect: genetics and heritability od Aoki, Hisaaki, Horie, Minoru

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Gender Differences in the Inheritance Mode of RYR2 Mutations in Catecholaminergic Polymorphic Ventricular Tachycardia Patients od Ohno, Seiko, Hasegawa, Kanae, Horie, Minoru

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Association between Progressive Intraventricular Conduction Disturbance and Cardiovascular Events od Hayashi, Hideki, Wu, Qi, Horie, Minoru

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Genetics of Brugada syndrome od Juang, Jyh-Ming Jimmy, Horie, Minoru

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The relationship between J waves and contact of lung cancer with the heart od Hayashi, Hideki, Wu, Qi, Horie, Minoru

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Effect of Flecainide on T‐Wave Alternans in Andersen–Tawil Syndrome od Hayashi, Hideki, Kawaguchi, Tamiro, Horie, Minoru

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Correction: Gender Differences in the Inheritance Mode of RYR2 Mutations in Catecholaminergic Polymorphic Ventricular Tachycardia Patients od Ohno, Seiko, Hasegawa, Kanae, Horie, Minoru

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Phospholipase C-linked receptors regulate the ATP-sensitive potassium channel by means of phosphatidylinositol 4,5-bisphosphate metabolism od Xie, Lai-Hua, Horie, Minoru, Takano, Makoto

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Molecular pathogenesis of long QT syndrome type 1 od Wu, Jie, Ding, Wei-Guang, Horie, Minoru

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The role of impaired sympathetic nerve function in enhancing coronary vasoconstriction in patients with hypertrophic cardiomyopathy od Matsuo, Shinro, Matsumoto, Tetsuya, Nakae, Ichiro, Horie, Minoru

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Unique genetic background and outcome of non‐Caucasian Japanese probands with arrhythmogenic right ventricular dysplasia/cardiomyopathy od Wada, Yuko, Ohno, Seiko, Aiba, Takeshi, Horie, Minoru

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Bradycardia Is a Specific Phenotype of Catecholaminergic Polymorphic Ventricular Tachycardia Induced by RYR2 Mutations od Miyata, Kazuaki, Ohno, Seiko, Itoh, Hideki, Horie, Minoru

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Cytoplasmic terminus domains of Kir6.x confer different nucleotide-dependent gating on the ATP-sensitive K(+) channel od Takano, Makoto, Xie, Lai-Hua, Otani, Hideo, Horie, Minoru

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Cardiac conduction defects and Brugada syndrome: A family with overlap syndrome carrying a nonsense SCN5A mutation() od Aoki, Hisaaki, Nakamura, Yoshihide, Ohno, Seiko, Makiyama, Takeru, Horie, Minoru

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Postoperative supraventricular tachycardia and polymorphic ventricular tachycardia due to a novel SCN5A variant: a case report of a rare comorbidity that is difficult to diagnose od Kato, Koichi, Ozawa, Tomoya, Ohno, Seiko, Nakagawa, Yoshihisa, Horie, Minoru

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Cardiac scintigraphic findings of mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes: A case report od Matsuo, Shinro, Nakajima, Kenichi, Kinuya, Seigo, Sato, Yuichi, Matsumoto, Naoya, Horie, Minoru

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Prognostic value of iodine-123 metaiodobenzylguanidine imaging in patients with heart failure od Matsuo, Shinro, Nakamura, Yasuyuki, Matsumoto, Tetsuya, Nakae, Ichiro, Murata, Kiyoshi, Horie, Minoru

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Three cases of catecholaminergic polymorphic ventricular tachycardia with prolonged QT intervals including two cases of compound mutations od Saito, Aki, Ohno, Seiko, Nuruki, Norihito, Nomura, Yuichi, Horie, Minoru, Yoshinaga, Masao

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A novel CACNA1C mutation identified in a patient with Timothy syndrome without syndactyly exerts both marked loss- and gain-of-function effects od Ozawa, Junichi, Ohno, Seiko, Saito, Hideki, Saitoh, Akihiko, Matsuura, Hiroshi, Horie, Minoru

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