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Takeru Makiyama
Takeru Makiyama
在 kuhp.kyoto-u.ac.jp 的电子邮件经过验证
标题
引用次数
引用次数
年份
Persistently increased serum concentrations of cardiac troponin T in patients with idiopathic dilated cardiomyopathy are predictive of adverse outcomes
Y Sato, T Yamada, R Taniguchi, K Nagai, T Makiyama, H Okada, ...
Circulation 103 (3), 369-374, 2001
4382001
Ultrastructural maturation of human-induced pluripotent stem cell-derived cardiomyocytes in a long-term culture
T Kamakura, T Makiyama, K Sasaki, Y Yoshida, Y Wuriyanghai, J Chen, ...
Circulation Journal 77 (5), 1307-1314, 2013
3402013
The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome
N Makita, E Behr, W Shimizu, M Horie, A Sunami, L Crotti, E Schulze-Bahr, ...
The Journal of clinical investigation 118 (6), 2219-2229, 2008
2692008
A Novel SCN5A Gain-of-Function Mutation M1875T Associated With Familial Atrial Fibrillation
T Makiyama, M Akao, S Shizuta, T Doi, K Nishiyama, Y Oka, S Ohno, ...
Journal of the American College of Cardiology 52 (16), 1326-1334, 2008
2502008
High prevalence of early repolarization in short QT syndrome
H Watanabe, T Makiyama, T Koyama, PJ Kannankeril, S Seto, K Okamura, ...
Heart rhythm 7 (5), 647-652, 2010
2112010
Electrocardiographic Characteristics and SCN5A Mutations in Idiopathic Ventricular Fibrillation Associated With Early Repolarization
H Watanabe, A Nogami, K Ohkubo, H Kawata, Y Hayashi, T Ishikawa, ...
Circulation: Arrhythmia and Electrophysiology 4 (6), 874-881, 2011
2092011
The genetics underlying acquired long QT syndrome: impact for genetic screening
H Itoh, L Crotti, T Aiba, C Spazzolini, I Denjoy, V Fressart, K Hayashi, ...
European heart journal 37 (18), 1456-1464, 2016
1962016
D85N, a KCNE1 polymorphism, is a disease-causing gene variant in long QT syndrome
Y Nishio, T Makiyama, H Itoh, T Sakaguchi, S Ohno, YZ Gong, ...
Journal of the American College of Cardiology 54 (9), 812-819, 2009
1792009
High Risk for Bradyarrhythmic Complications in Patients With Brugada Syndrome Caused by SCN5AGene Mutations
T Makiyama, M Akao, K Tsuji, T Doi, S Ohno, K Takenaka, A Kobori, ...
Journal of the American College of Cardiology 46 (11), 2100-2106, 2005
1712005
Genotype-Phenotype Correlation of SCN5A Mutation for the Clinical and Electrocardiographic Characteristics of Probands With Brugada Syndrome: A Japanese …
K Yamagata, M Horie, T Aiba, S Ogawa, Y Aizawa, T Ohe, M Yamagishi, ...
Circulation 135 (23), 2255-2270, 2017
1702017
KCNE5 (KCNE1L) Variants Are Novel Modulators of Brugada Syndrome and Idiopathic Ventricular Fibrillation
S Ohno, DP Zankov, WG Ding, H Itoh, T Makiyama, T Doi, S Shizuta, ...
Circulation: Arrhythmia and Electrophysiology 4 (3), 352-361, 2011
1532011
Anticoagulation therapy for venous thromboembolism in the real world―From the COMMAND VTE Registry―
Y Yamashita, T Morimoto, H Amano, T Takase, S Hiramori, K Kim, ...
Circulation Journal 82 (5), 1262-1270, 2018
1372018
Latent genetic backgrounds and molecular pathogenesis in drug-induced long-QT syndrome
H Itoh, T Sakaguchi, WG Ding, E Watanabe, I Watanabe, Y Nishio, ...
Circulation: Arrhythmia and Electrophysiology 2 (5), 511-523, 2009
1262009
Long QT syndrome with compound mutations is associated with a more severe phenotype: a Japanese multicenter study
H Itoh, W Shimizu, K Hayashi, K Yamagata, T Sakaguchi, S Ohno, ...
Heart Rhythm 7 (10), 1411-1418, 2010
1192010
Impact of CYP2C19 polymorphisms on the antiplatelet effect of clopidogrel in an actual clinical setting in Japan
T Jinnai, H Horiuchi, T Makiyama, J Tazaki, T Tada, M Akao, K Ono, ...
Circulation Journal 73 (8), 1498-1503, 2009
1162009
Phenotype Variability in Patients Carrying KCNJ2 Mutations
H Kimura, J Zhou, M Kawamura, H Itoh, Y Mizusawa, WG Ding, J Wu, ...
Circulation: Cardiovascular Genetics 5 (3), 344-353, 2012
1122012
Transethnic genome-wide association study provides insights in the genetic architecture and heritability of long QT syndrome
N Lahrouchi, R Tadros, L Crotti, Y Mizusawa, PG Postema, L Beekman, ...
Circulation 142 (4), 324-338, 2020
1112020
Allele-specific ablation rescues electrophysiological abnormalities in a human iPS cell model of long-QT syndrome with a CALM2 mutation
Y Yamamoto, T Makiyama, T Harita, K Sasaki, Y Wuriyanghai, M Hayano, ...
Human Molecular Genetics 26 (9), 1670-1677, 2017
1082017
Exon 3 deletion of RYR2 encoding cardiac ryanodine receptor is associated with left ventricular non-compaction
S Ohno, M Omura, M Kawamura, H Kimura, H Itoh, T Makiyama, ...
Europace 16 (11), 1646-1654, 2014
1032014
Long-term follow-up of a pediatric cohort with short QT syndrome
J Villafañe, J Atallah, MH Gollob, P Maury, C Wolpert, R Gebauer, ...
Journal of the American College of Cardiology 61 (11), 1183-1191, 2013
1032013
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