38 Publications (Page 2 of 2)
2010
Long QT syndrome with compound mutations is associated with a more severe phenotype: a Japanese multicenter study.
Itoh, Hideki⋅Shimizu, Wataru⋅Hayashi, Kenshi⋅Yamagata, Kenichiro⋅Sakaguchi, Tomoko⋅Ohno, Seiko⋅Makiyama, Takeru⋅Akao, Masaharu⋅Ai, Tomohiko⋅Noda, Takashi⋅Miyazaki, Aya⋅Miyamoto, Yoshihiro⋅Yamagishi, Masakazu⋅Kamakura, Shiro and Horie, Minoru
Heart rhythm : the official journal of the Heart Rhythm Society, vol. 7, (no. 10), pp. 1411-8, 2010/Oct. | Journal Article
2009
20p12.3 microdeletion predisposes to Wolff-Parkinson-White syndrome with variable neurocognitive deficits.
Lalani, Seema R⋅Thakuria, J V⋅Cox, G F⋅Wang, X⋅Bi, W⋅Bray, M S⋅Shaw, C⋅Cheung, Steven W⋅Chinault, A C⋅Boggs, B A⋅Ou, Z⋅Brundage, E K⋅Lupski, J R⋅Gentile, J⋅Waisbren, S⋅Pursley, A⋅Ma, L⋅Khajavi, M⋅Zapata, G⋅Friedman, R⋅Kim, J J⋅Towbin, J A⋅Stankiewicz, P⋅Schnittger, S⋅Hansmann, I⋅Ai, Tomohiko⋅Sood, S⋅Wehrens, Xander H⋅Martin, J F⋅Belmont, J W and Potocki, L
Journal of medical genetics, vol. 46, (no. 3), pp. 168-75, 2009/Mar. | Journal Article
 
A Nonsense SCN5A Mutation Associated with Brugada-Type Electrocardiogram and Intraventricular Conduction Defects
SAMANI, KAVEH⋅Ai, Tomohiko⋅Towbin, Jeffrey A⋅BRUGADA, RAMON⋅SHURAIH, MOSSAAB⋅XI, YUTAO⋅WU, GERU⋅CHENG, JIE and Vatta, Matteo
Pacing and Clinical Electrophysiology, vol. 32, (no. 9), pp. 1231-1236, 2009. | Journal Article
 
A novel SCN5A mutation V1340I in Brugada syndrome augmenting arrhythmias during febrile illness.
Samani, Kaveh⋅Wu, Geru⋅Ai, Tomohiko⋅Shuraih, Mossaab⋅Mathuria, Nilesh S⋅Li, Zhaohui⋅Sohma, Yoshiro⋅Purevjav, Enkhsaikhan⋅Xi, Yutao⋅Towbin, Jeffrey A⋅Cheng, Jie and Vatta, Matteo
Heart rhythm : the official journal of the Heart Rhythm Society, vol. 6, (no. 9), pp. 1318-26, 2009/Sep. | Journal Article
2008
alpha-1-syntrophin mutation and the long-QT syndrome: a disease of sodium channel disruption.
Wu, Geru⋅Ai, Tomohiko⋅Kim, Jeffrey J⋅Mohapatra, Bhagyalaxmi⋅Xi, Yutao⋅Li, Zhaohui⋅Abbasi, Shahrzad⋅Purevjav, Enkhsaikhan⋅Samani, Kaveh⋅Ackerman, Michael J⋅Qi, Ming⋅Moss, Arthur J⋅Shimizu, Wataru⋅Towbin, Jeffrey A⋅Cheng, Jie and Vatta, Matteo
Circulation. Arrhythmia and electrophysiology, vol. 1, (no. 3), pp. 193-201, 2008/Aug. | Journal Article
2007
A common SCN5A variant alters the responsiveness of human sodium channels to class I antiarrhythmic agents.
Shuraih, Mossaab⋅Ai, Tomohiko⋅Vatta, Matteo⋅Sohma, Yoshiro⋅Merkle, Eileen M⋅Taylor, Erica⋅Li, Zhaohui⋅Xi, Yutao⋅Razavi, Mehdi⋅Towbin, Jeffrey A and Cheng, Jie
Journal of cardiovascular electrophysiology, vol. 18, (no. 4), pp. 434-40, 2007/Apr. | Journal Article
2006
Slow pathway ablation decreases vulnerability to pacing-induced atrial fibrillation: Possible role of vagal denervation.
Razavi, Mehdi⋅Cheng, Jie⋅Rasekh, Abdi⋅Yang, Donghui⋅Delapasse, Scott⋅Ai, Tomohiko⋅Meade, Thomas⋅Donsky, Alan⋅Goodman, Mary J and Massumi, Ali
Pacing and clinical electrophysiology : PACE, vol. 29, (no. 11), pp. 1234-9, 2006/Nov. | Journal Article
2004
Capsaicin potentiates wild-type and mutant cystic fibrosis transmembrane conductance regulator chloride-channel currents.
Ai, Tomohiko⋅Bompadre, Silvia G⋅Wang, Xiaohui⋅Hu, Shenghui⋅Li, Min and Hwang, Tzyh Chang
Molecular pharmacology, vol. 65, (no. 6), pp. 1415-26, 2004/Jun. | Journal Article
 
Direct effects of 9-anthracene compounds on cystic fibrosis transmembrane conductance regulator gating.
Ai, Tomohiko⋅Bompadre, Silvia G⋅Sohma, Yoshiro⋅Wang, Xiaohui⋅Li, Min and Hwang, Tzyh Chang
Pflügers Archiv : European journal of physiology, vol. 449, (no. 1), pp. 88-95, 2004/Oct. | Journal Article
2003
Exercise stress test amplifies genotype-phenotype correlation in the LQT1 and LQT2 forms of the long-QT syndrome.
Takenaka, Kotoe⋅Ai, Tomohiko⋅Shimizu, Wataru⋅Kobori, Atsushi⋅Ninomiya, Tomonori⋅Otani, Hideo⋅Kubota, Tomoyuki⋅Takaki, Hiroshi⋅Kamakura, Shiro and Horie, Minoru
Circulation, vol. 107, (no. 6), pp. 838-44, 2003/Feb/18. | Journal Article
2002
Drug-induced long-QT syndrome associated with a subclinical SCN5A mutation.
Makita, Naomasa⋅Makita, Naomasa⋅Horie, Minoru⋅Horie, Minoru⋅Nakamura, Takeshi⋅Nakamura, Takeshi⋅Ai, Tomohiko⋅Ai, Tomohiko⋅Sasaki, Koji⋅Sasaki, Koji⋅Yokoi, Hisataka⋅Yokoi, Hisataka⋅Sakurai, Masayuki⋅Sakurai, Masayuki⋅Sakuma, Ichiro⋅Sakuma, Ichiro⋅Otani, Hideo⋅Otani, Hideo⋅Sawa, Hirofumi⋅Sawa, Hirofumi⋅Kitabatake, Akira and Kitabatake, Akira
Circulation, vol. 106, (no. 10), pp. 1269-74, 2002/Sep/3. | Journal Article
 
Novel KCNJ2 mutation in familial periodic paralysis with ventricular dysrhythmia.
Ai, Tomohiko⋅Fujiwara, Yuichiro⋅Tsuji, Keiko⋅Otani, Hideo⋅Nakano, Shozo⋅Kubo, Yoshihiro and Horie, Minoru
Circulation, vol. 105, (no. 22), pp. 2592-4, 2002/Jun/4. | Journal Article
1997
Insulin secretion and its modulation by antiarrhythmic and sulfonylurea drugs.
Horie, M⋅Ishida-Takahashi, A⋅Ai, T⋅Nishimoto, T⋅Tsuura, Y⋅Ishida, H⋅Seino, Y and Sasayama, S
Cardiovascular research, vol. 34, (no. 1), pp. 69-72, April 1997. | Journal Article