Analysis of the shape of the T-wave in congenital long-QT syndrome type 3 by geometric morphometrics

Por Horigome, Hitoshi, Ishikawa, Yasuhiro, Takahashi, Kazuhiro, Yoshinaga, Masao, Sumitomo, Naokata
Publicado no Sci Rep (2021)

Vancomycin-Resistant Enterococci in Humans and Imported Chickens in Japan

Por Ozawa, Yoshiyuki, Tanimoto, Koichi, Nomura, Takahiro, Yoshinaga, Masao, Arakawa, Yoshichika, Ike, Yasuyoshi
Publicado em 2002

Three cases of catecholaminergic polymorphic ventricular tachycardia with prolonged QT intervals including two cases of compound mutations

Por Saito, Aki, Ohno, Seiko, Nuruki, Norihito, Nomura, Yuichi, Horie, Minoru, Yoshinaga, Masao
Publicado no J Arrhythm (2018)

Risk factors for development of ventricular tachycardia in patients with ventricular premature contraction with a structurally normal heart

Por Nomura, Yuichi, Seki, Syunji, Hazeki, Daisuke, Ueno, Kentaro, Tanaka, Yuji, Masuda, Kiminori, Nishibatake, Makoto, Yoshinaga, Masao
Publicado no J Arrhythm (2019)

Prediagnostic electrocardiographic and echocardiographic findings of biopsy‐proven hypertrophic cardiomyopathy

Por Seki, Shunji, Yamashita, Erika, Tanoue, Kazuyuki, Nuruki, Norihito, Sonoda, Masahiro, Ohno, Seiko, Ishibashi‐Ueda, Hatsue, Tanaka, Yuji, Yoshinaga, Masao
Publicado no J Arrhythm (2018)

Multivariate analysis of TU wave complex on electrocardiogram in Andersen–Tawil syndrome with KCNJ2 mutations

Por Horigome, Hitoshi, Ishikawa, Yasuhiro, Kokubun, Norito, Yoshinaga, Masao, Sumitomo, Naokata, Lin, Lisheng, Kato, Yoshiaki, Tanabe‐Kameda, Yuri, Ohno, Seiko, Nagashima, Masami, Horie, Minoru
Publicado no Ann Noninvasive Electrocardiol (2019)

Typical Enteroaggregative Escherichia coli Is the Most Prevalent Pathotype among E. coli Strains Causing Diarrhea in Mongolian Children

Por Sarantuya, Jav, Nishi, Junichiro, Wakimoto, Naoko, Erdene, Shirchin, Nataro, James P., Sheikh, Jalaluddin, Iwashita, Mayumi, Manago, Kunihiro, Tokuda, Koichi, Yoshinaga, Masao, Miyata, Koichiro, Kawano, Yoshifumi
Publicado em 2004

Association of Genetic and Clinical Aspects of Congenital Long QT Syndrome With Life-Threatening Arrhythmias in Japanese Patients

Por Shimizu, Wataru, Makimoto, Hisaki, Yamagata, Kenichiro, Kamakura, Tsukasa, Wada, Mitsuru, Miyamoto, Koji, Inoue-Yamada, Yuko, Okamura, Hideo, Ishibashi, Kohei, Noda, Takashi, Nagase, Satoshi, Miyazaki, Aya, Sakaguchi, Heima, Shiraishi, Isao, Makiyama, Takeru, Ohno, Seiko, Itoh, Hideki, Watanabe, Hiroshi, Hayashi, Kenshi, Yamagishi, Masakazu, Morita, Hiroshi, Yoshinaga, Masao, Aizawa, Yoshiyasu, Kusano, Kengo, Miyamoto, Yoshihiro, Kamakura, Shiro, Yasuda, Satoshi, Ogawa, Hisao, Tanaka, Toshihiro, Sumitomo, Naotaka, Hagiwara, Nobuhisa, Fukuda, Keiichi, Ogawa, Satoshi, Aizawa, Yoshifusa, Makita, Naomasa, Ohe, Tohru, Horie, Minoru, Aiba, Takeshi
Publicado no JAMA Cardiol (2019)

Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome

Por Lahrouchi, Najim, Tadros, Rafik, Crotti, Lia, Mizusawa, Yuka, Postema, Pieter G., Beekman, Leander, Walsh, Roddy, Hasegawa, Kanae, Barc, Julien, Ernsting, Marko, Turkowski, Kari L., Mazzanti, Andrea, Beckmann, Britt M., Shimamoto, Keiko, Diamant, Ulla-Britt, Wijeyeratne, Yanushi D., Kucho, Yu, Robyns, Tomas, Ishikawa, Taisuke, Arbelo, Elena, Christiansen, Michael, Winbo, Annika, Jabbari, Reza, Lubitz, Steven A., Steinfurt, Johannes, Rudic, Boris, Loeys, Bart, Shoemaker, M. Ben, Weeke, Peter E., Pfeiffer, Ryan, Davies, Brianna, Andorin, Antoine, Hofman, Nynke, Dagradi, Federica, Pedrazzini, Matteo, Tester, David J., Bos, J. Martijn, Sarquella-Brugada, Georgia, Campuzano, Óscar, Platonov, Pyotr G., Stallmeyer, Birgit, Zumhagen, Sven, Nannenberg, Eline A., Veldink, Jan H., van den Berg, Leonard H., Al-Chalabi, Ammar, Shaw, Christopher E., Shaw, Pamela J., Morrison, Karen E., Andersen, Peter M., Müller-Nurasyid, Martina, Cusi, Daniele, Barlassina, Cristina, Galan, Pilar, Lathrop, Mark, Munter, Markus, Werge, Thomas, Ribasés, Marta, Aung, Tin, Khor, Chiea C., Ozaki, Mineo, Lichtner, Peter, Meitinger, Thomas, van Tintelen, J. Peter, Hoedemaekers, Yvonne, Denjoy, Isabelle, Leenhardt, Antoine, Napolitano, Carlo, Shimizu, Wataru, Schott, Jean-Jacques, Gourraud, Jean-Baptiste, Makiyama, Takeru, Ohno, Seiko, Itoh, Hideki, Krahn, Andrew D., Antzelevitch, Charles, Roden, Dan M., Saenen, Johan, Borggrefe, Martin, Odening, Katja E., Ellinor, Patrick T., Tfelt-Hansen, Jacob, Skinner, Jonathan R., van den Berg, Maarten P., Olesen, Morten Salling, Brugada, Josep, Brugada, Ramón, Makita, Naomasa, Breckpot, Jeroen, Yoshinaga, Masao, Behr, Elijah R., Rydberg, Annika, Aiba, Takeshi, Kääb, Stefan, Priori, Silvia G., Guicheney, Pascale, Tan, Hanno L., Newton-Cheh, Christopher, Ackerman, Michael J., Schwartz, Peter J., Schulze-Bahr, Eric, Probst, Vincent, Horie, Minoru, Wilde, Arthur A., Tanck, Michael W.T., Bezzina, Connie R.
Publicado no Circulation (2020)

Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

Por Walsh, Roddy, Lahrouchi, Najim, Tadros, Rafik, Kyndt, Florence, Glinge, Charlotte, Postema, Pieter G., Amin, Ahmad S., Nannenberg, Eline A., Ware, James S., Whiffin, Nicola, Mazzarotto, Francesco, Škorić-Milosavljević, Doris, Krijger, Christian, Arbelo, Elena, Babuty, Dominique, Barajas-Martinez, Hector, Beckmann, Britt M., Bézieau, Stéphane, Bos, J. Martijn, Breckpot, Jeroen, Campuzano, Oscar, Castelletti, Silvia, Celen, Candan, Clauss, Sebastian, Corveleyn, Anniek, Crotti, Lia, Dagradi, Federica, de Asmundis, Carlo, Denjoy, Isabelle, Dittmann, Sven, Ellinor, Patrick T., Ortuño, Cristina Gil, Giustetto, Carla, Gourraud, Jean-Baptiste, Hazeki, Daisuke, Horie, Minoru, Ishikawa, Taisuke, Itoh, Hideki, Kaneko, Yoshiaki, Kanters, Jørgen K., Kimoto, Hiroki, Kotta, Maria-Christina, Krapels, Ingrid P. C., Kurabayashi, Masahiko, Lazarte, Julieta, Leenhardt, Antoine, Loeys, Bart L., Lundin, Catarina, Makiyama, Takeru, Mansourati, Jacques, Martins, Raphaël P., Mazzanti, Andrea, Mörner, Stellan, Napolitano, Carlo, Ohkubo, Kimie, Papadakis, Michael, Rudic, Boris, Molina, Maria Sabater, Sacher, Frédéric, Sahin, Hatice, Sarquella-Brugada, Georgia, Sebastiano, Regina, Sharma, Sanjay, Sheppard, Mary N., Shimamoto, Keiko, Shoemaker, M. Benjamin, Stallmeyer, Birgit, Steinfurt, Johannes, Tanaka, Yuji, Tester, David J., Usuda, Keisuke, van der Zwaag, Paul A., Van Dooren, Sonia, Van Laer, Lut, Winbo, Annika, Winkel, Bo G., Yamagata, Kenichiro, Zumhagen, Sven, Volders, Paul G. A., Lubitz, Steven A., Antzelevitch, Charles, Platonov, Pyotr G., Odening, Katja E., Roden, Dan M., Roberts, Jason D., Skinner, Jonathan R., Tfelt-Hansen, Jacob, van den Berg, Maarten P., Olesen, Morten S., Lambiase, Pier D., Borggrefe, Martin, Hayashi, Kenshi, Rydberg, Annika, Nakajima, Tadashi, Yoshinaga, Masao, Saenen, Johan B., Kääb, Stefan, Brugada, Pedro, Robyns, Tomas, Giachino, Daniela F., Ackerman, Michael J., Brugada, Ramon, Brugada, Josep, Gimeno, Juan R., Hasdemir, Can, Guicheney, Pascale, Priori, Silvia G., Schulze-Bahr, Eric, Makita, Naomasa, Schwartz, Peter J., Shimizu, Wataru, Aiba, Takeshi, Schott, Jean-Jacques, Redon, Richard, Ohno, Seiko, Probst, Vincent, Behr, Elijah R., Barc, Julien, Bezzina, Connie R.
Publicado no Genet Med (2020)