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Education and qualifications (2)

Shiga Ika Daigaku: Otsu, Shiga, JP

2014-03-10 | PhD (Cardiovascular medicine)
Education
Source: Self-asserted source
koichi KATO

Shiga Ika Daigaku: Otsu, Shiga, JP

1999-04-01 to 2005-04-12 | MD
Education
Source: Self-asserted source
koichi KATO

Works (26)

SCN5A variant type-dependent risk prediction in Brugada syndrome

Europace
2025-02-05 | Journal article
DOI: 10.1093/europace/euaf024
Contributors: Takanori Aizawa; Takeru Makiyama; Hai Huang; Tomohiko Imamura; Megumi Fukuyama; Keiko Sonoda; Koichi Kato; Takashi Hisamatsu; Yuko Nakamura; Kenji Hoshino et al.
Source: check_circle
Crossref

Sex-specific clinical course of young patients with Brugada syndrome

European Heart Journal
2025-02-05 | Journal article
DOI: 10.1093/eurheartj/ehae739
Contributors: Tomohiko Imamura; Takeru Makiyama; Junichi Ozawa; Keiko Sonoda; Koichi Kato; Takanori Aizawa; Asami Kashiwa; Jingshan Gao; Hai Huang; Yuta Yamamoto et al.
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Crossref

Clinical characterization of type 1 long QT syndrome caused by C-terminus Kv7.1 variants

Heart Rhythm
2024-02 | Journal article
DOI: 10.1016/j.hrthm.2024.02.021
Part of ISSN: 1547-5271
Contributors: Asami Kashiwa; Hideki Itoh; Takeru Makiyama; Yuko Wada; Junichi Ozawa; Koichi Kato; Megumi Fukuyama; Tadashi Nakajima; Seiko Ohno; Minoru Horie
Source: Self-asserted source
koichi KATO

Non-missense variants of KCNH2 show better outcomes in type 2 long QT syndrome

EP Europace
2023-04-15 | Journal article
DOI: 10.1093/europace/euac269
Contributors: Takanori Aizawa; Yuko Wada; Kanae Hasegawa; Hai Huang; Tomohiko Imamura; Jingshan Gao; Asami Kashiwa; Hirohiko Kohjitani; Megumi Fukuyama; Koichi Kato et al.
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Crossref

Case report: Vascular graft infection due to Aspergillus species presenting with recurrent vascular occlusion

BMC Cardiovascular Disorders
2022-12 | Journal article
DOI: 10.1186/s12872-022-02571-3
Contributors: Ayami Tano; Koichi Kato; Yoshimasa Seike; Hitoshi Matsuda; Takashi Suzue; Yoshihiro Kaneko; Misato Kodama; Yuichi Sawayama; Akashi Miyamoto; Noriaki Yagi et al.
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Crossref

Novel CALM3 Variant Causing Calmodulinopathy With Variable Expressivity in a 4-Generation Family

Circulation: Arrhythmia and Electrophysiology
2022-03 | Journal article
DOI: 10.1161/CIRCEP.121.010572
Contributors: Koichi Kato; Holly M. Isbell; Véronique Fressart; Isabelle Denjoy; Amal Debbiche; Hideki Itoh; Jacques Poinsot; Alfred L. George, Jr; Alain Coulombe; Madeline A. Shea et al.
Source: check_circle
Crossref

Impact of cascade screening for catecholaminergic polymorphic ventricular tachycardia type 1.

Heart (British Cardiac Society)
2022-02-08 | Journal article
DOI: 10.1136/heartjnl-2021-320220
PMID: 35135837
Source: Self-asserted source
koichi KATO

Successful management of a Young Athlete with Type 2 Long QT Syndrome by Genotype-specific Risk Stratification and Bridging Therapy with a Wearable Cardioverter Defibrillator: A Case Report

Internal Medicine
2022-02-01 | Journal article
DOI: 10.2169/internalmedicine.8093-21
Part of ISSN: 0918-2918
Part of ISSN: 1349-7235
Source: Self-asserted source
koichi KATO

School-based routine screenings of electrocardiograms for the diagnosis of long QT syndrome

EP Europace
2022-01-21 | Journal article
DOI: 10.1093/europace/euab320
Part of ISSN: 1099-5129
Part of ISSN: 1532-2092
Source: Self-asserted source
koichi KATO
grade
Preferred source (of 2)‎

An International Multi-Center Cohort Study on β-blockers for the Treatment of Symptomatic Children with Catecholaminergic Polymorphic Ventricular Tachycardia.

Circulation
2021-12-07 | Journal article
DOI: 10.1161/circulationaha.121.056018
PMID: 34874747
Source: Self-asserted source
koichi KATO

Loss-of-function mutations in cardiac ryanodine receptor channel cause various types of arrhythmias including long QT syndrome.

Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology
2021-10-18 | Journal article
DOI: 10.1093/europace/euab250
PMID: 34661651
Source: Self-asserted source
koichi KATO

Diverse phenotypic expression associated with the same genetic variant in female heterozygote patients of Anderson–Fabry disease: a case series

European Heart Journal - Case Reports
2021-02-04 | Journal article
DOI: 10.1093/ehjcr/ytaa538
Contributors: Daisuke Tomioka; Koichi Kato; Tomoya Ozawa; Kenji Kodama; Hiroaki Takahashi; Kenichi Dochi; Yoshiki Ueno; Yoshihisa Nakagawa; Erik Holy; Zaid Iskander et al.
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Crossref

LMNA Missense Mutation Causes Nonsense-Mediated mRNA Decay and Severe Dilated Cardiomyopathy

Circulation: Genomic and Precision Medicine
2020-10-20 | Journal article
DOI: 10.1161/CIRCGEN.119.002853
Contributors: Koichi Kato; Seiko Ohno; Keiko Sonoda; Megumi Fukuyama; Takeru Makiyama; Tomoya Ozawa; Minoru Horie
Source: check_circle
Crossref

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.

BMC cardiovascular disorders
2020-07 | Journal article
DOI: 10.1186/s12872-020-01601-2
PMID: 32615940
PMC: PMC7333335
Contributors: Kato K; Ozawa T; Ohno S; Nakagawa Y; Horie M
Source: Self-asserted source
koichi KATO via Europe PubMed Central

Left-dominant arrhythmogenic cardiomyopathy with a nonsense mutation in DSP.

ESC heart failure
2020-06 | Journal article
DOI: 10.1002/ehf2.12790
PMID: 32592540
Contributors: Tsuruta Y; Sueta D; Takashio S; Oda S; Sakamoto K; Kaikita K; Kato K; Ohno S; Horie M; Tsujita K
Source: Self-asserted source
koichi KATO via Europe PubMed Central

High Prevalence of Late-Appearing T-Wave in Patients With Long QT Syndrome Type 8.

Circulation journal : official journal of the Japanese Circulation Society
2020-03 | Journal article
DOI: 10.1253/circj.cj-19-1101
PMID: 32161207
Contributors: Fukuyama M; Ohno S; Ozawa J; Kato K; Makiyama T; Nakagawa Y; Horie M
Source: Self-asserted source
koichi KATO via Europe PubMed Central

An African loss-of-function CACNA1C variant p.T1787M associated with a risk of ventricular fibrillation.

Scientific reports
2018-10 | Journal article
DOI: 10.1038/s41598-018-32867-4
PMID: 30279520
PMC: PMC6168548
Contributors: Blancard M; Debbiche A; Kato K; Cardin C; Sabrina G; Gandjbakhch E; Probst V; Haissaguerre M; Extramiana F; Hocini M et al.
Source: Self-asserted source
koichi KATO via Europe PubMed Central

Clinical Manifestations and Long-Term Mortality in Lamin A/C Mutation Carriers From a Japanese Multicenter Registry.

Circulation journal : official journal of the Japanese Circulation Society
2018-08 | Journal article
DOI: 10.1253/circj.cj-18-0339
PMID: 30078822
Contributors: Nakajima K; Aiba T; Makiyama T; Nishiuchi S; Ohno S; Kato K; Yamamoto Y; Doi T; Shizuta S; Onoue K et al.
Source: Self-asserted source
koichi KATO via Europe PubMed Central

Novel intracellular transport-refractory mutations in KCNH2 identified in patients with symptomatic long QT syndrome.

Journal of cardiology
2017-11 | Journal article
DOI: 10.1016/j.jjcc.2017.10.004
PMID: 29146210
Contributors: Fukumoto D; Ding WG; Wada Y; Fujii Y; Ichikawa M; Takayama K; Fukuyama M; Kato K; Itoh H; Makiyama T et al.
Source: Self-asserted source
koichi KATO via Europe PubMed Central

Quantitative analysis of PKP2 and neighbouring genes in a patient with arrhythmogenic right ventricular cardiomyopathy caused by heterozygous PKP2 deletion.

Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology
2017-04 | Journal article
DOI: 10.1093/europace/euw038
PMID: 28431057
Contributors: Sonoda K; Ohno S; Otuki S; Kato K; Yagihara N; Watanabe H; Makiyama T; Minamino T; Horie M
Source: Self-asserted source
koichi KATO via Europe PubMed Central

Multigenerational Inheritance of Long QT Syndrome Type 2 in a Japanese Family.

Internal medicine (Tokyo, Japan)
2016-02 | Journal article
DOI: 10.2169/internalmedicine.55.6014
PMID: 26831020
Contributors: Ichikawa M; Ohno S; Fujii Y; Ozawa J; Sonoda K; Fukuyama M; Kato K; Kimura H; Itoh H; Hayashi H et al.
Source: Self-asserted source
koichi KATO via Europe PubMed Central

A Common Mutation of Long QT Syndrome Type 1 in Japan.

Circulation Journal
2015 | Journal article
DOI: 10.1253/circj.CJ-15-0342
PMID: 26118460
Source: Self-asserted source
koichi KATO
grade
Preferred source (of 2)‎

LMNA cardiomyopathy detected in Japanese arrhythmogenic right ventricular cardiomyopathy cohort.

Journal of Cardiology
2015-11 | Journal article
PMID: 26620845
Source: Self-asserted source
koichi KATO
grade
Preferred source (of 2)‎

Long QT syndrome type 8: novel CACNA1C mutations causing QT prolongation and variant phenotypes.

EP Europace
2014-12 | Journal article
DOI: 10.1093/europace/euu063
PMID: 24728418
Source: Self-asserted source
koichi KATO
grade
Preferred source (of 2)‎

A molecular mechanism for adrenergic-induced long QT syndrome.

Journal of the American College of Cardiology
2014-03 | Journal article
DOI: 10.1016/j.jacc.2013.08.1648
PMID: 24184248
Source: Self-asserted source
koichi KATO
grade
Preferred source (of 2)‎

Cardiac channelopathies associated with infantile fatal ventricular arrhythmias: from the cradle to the bench.

Journal of Cardiovascular Electrophysiology
2014-01 | Journal article
DOI: 10.1111/jce.12270
PMID: 24112685
Source: Self-asserted source
koichi KATO
grade
Preferred source (of 2)‎
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