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Nagasaki University Graduate School of Biomedical Sciences 長崎大学学院医歯薬学総合研究科
 

News

A Japanese Long QT registry paper was accepted in JAMA Cardiolol.

Shimizu W, Makimoto H, Yamagata K, Kamakura T, Wada M, Miyamoto K, Inoue-Yamada Y, Okamura H, Ishibashi K, Noda T, Nagase S, Miyazaki A, Sakaguchi H, Shiraishi I, Makiyama T, Ohno S, Itoh H, Watanabe H, Hayashi K, Yamagishi M, Morita H, Yoshinaga M, Aizawa Y, Kusano K, Miyamoto Y, Kamakura S, Yasuda S, Ogawa H, Tanaka T, Sumitomo N, Hagiwara N, Fukuda K, Ogawa S, Aizawa Y, Makita N, Ohe T, Horie M, Aiba T.
Association of Genetic and Clinical Aspects of Congenital Long QT Syndrome With Life-Threatening Arrhythmias in Japanese PatientsAssociation of Genetic and Clinical Aspects of Long QT Syndrome With ArrhythmiasAssociation of Genetic and Clinical Aspects of Long QT Syndrome With Arrhythmias.
JAMA Cardiol 2019;in press. doi:10.1001/jamacardio.2018.4925

A collaborative paper about laminopathy with NCVC was accepted for publication in Circ J

Clinical Manifestations and Long-term Mortality in Lamin A/C Mutation Carriers from the Japanese Multicenter Registry

Nakajima, Kenzaburo; Aiba, Takeshi; Makiyama, Takeru; Nishiuchi, Suguru; Ohno, Seiko; Kato, Koichi; Yamamoto, Yuta; Doi, Takahiro; Shizuta, Satoshi; Onoue, Kenji; Yagihara, Nobue; Ishikawa, Taisuke; Watanabe, Ichiro; Kawakami, Hiroshi; Oginosawa, Yasushi; Murakoshi, Nobuyuki; Nogami, Akihiko; Aonuma, Kazutaka; Saito, Yoshihiko; Kimura, Takeshi; Yasuda, Satoshi; Makita, Naomasa; Shimizu, Wataru; Horie, Minoru; Kusano, Kengo:
Circ J 2018in press

A collaborative paper with Dr Nakano in Hiroshima Univ was accepted in Circulation: Genomic and Precision Medicine

HCN4 Gene polymorphisms are Associated with Occurrence of Tachycardia Induced Cardiomyopathy in Patients with Atrial Fibrillation

Yukiko Nakano, Hidenori Ochi, Akinori Sairaku, Yuko Onohara , Takehito Tokuyama, Chikaaki Motoda, Hiroya Matsumura, Shunsuke Tomomori, Michitaka Amioka, Naoya Hironobe, Yousaku Ohkubo, Shou Okamura, Naomasa Makita, Yukihiko Yoshida, Kazuaki Chayama, and Yasuki Kihara
Circ Genom Precis Med 2018, in press

An international collaboration paper about SCN1B mutations related to inherited lethal arrhythmia was accepted for publication in Heart Rhythm Journal.

Lack of genotype-phenotype correlation in Brugada syndrome and sudden arrhythmic death syndrome families with reported pathogenic SCN1B variants.
Belinda Gray, Can Hasdem, Jodie Ingles, Takeshi Aiba, Naomasa Makita, Vincent Probst, Arthur A.M.Wilde, Ruth Newbury-Ecob, Mary N Sheppard, Christopher Semsarian, Raymond W. Sy, Elijah R. Behr
Heart Rhythm 2018 (in press)

We had a Farewell and Welcome party for Mr.Hiroki Kimoto, Ms.Yumi Matsuo and Yoko Komori.

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