Inherited bradyarrhythmia: A diverse genetic background

por Ishikawa, Taisuke, Tsuji, Yukiomi, Makita, Naomasa
Publicado 2016

Dynamic QT response to cold‐water face immersion in long‐QT syndrome type 3

por Takahashi, Kazuhiro, Shimizu, Wataru, Makita, Naomasa, Nakayashiro, Mami
Publicado 2020

A novel de novo calmodulin mutation in a 6-year-old boy who experienced an aborted cardiac arrest

por Takahashi, Kazuhiro, Ishikawa, Taisuke, Makita, Naomasa, Takefuta, Kiyotaka, Nabeshima, Taisuke, Nakayashiro, Mami
Publicado 2016

Progressive atrial myocardial fibrosis in a 4-year-old girl with atrial standstill associated with an SCN5A gene mutation

por Kato, Yoshiaki, Nozaki, Yoshihiro, Takahashi-Igari, Miho, Sugano, Masato, Makita, Naomasa, Horigome, Hitoshi
Publicado 2022

Arrhythmogenic right ventricular cardiomyopathy in a Japanese patient with a homozygous founder variant of DSG2 in the East Asian population

por Murakami, Haruka, Tanimoto, Yoko, Tanimoto, Kojiro, Inoue, Satomi, Ishikawa, Taisuke, Makita, Naomasa, Yamazawa, Kazuki
Publicado 2022

Induction of Tissue Factor Expression in Endothelial Cells by Basic Fibroblast Growth Factor and its Modulation by Fenofibric acid

por Kaneko, Takeaki, Fujii, Satoshi, Matsumoto, Akio, Goto, Daisuke, Makita, Naomasa, Hamada, Junichi, Moriuchi, Tetsuya, Kitabatake, Akira
Publicado 2003

HCN4 pacemaker channels attenuate the parasympathetic response and stabilize the spontaneous firing of the sinoatrial node

por Kozasa, Yuko, Nakashima, Noriyuki, Ito, Masayuki, Ishikawa, Taisuke, Kimoto, Hiroki, Ushijima, Kazuo, Makita, Naomasa, Takano, Makoto
Publicado 2018

Desmin‐related myopathy characterized by non‐compaction cardiomyopathy, cardiac conduction defect, and coronary artery dissection

por Tamiya, Ran, Saito, Yuki, Fukamachi, Daisuke, Nagashima, Koichi, Aizawa, Yoshihiro, Ohkubo, Kimie, Hatta, Takumi, Sezai, Akira, Tanaka, Masashi, Ishikawa, Taisuke, Makita, Naomasa, Sumitomo, Naokata, Okumura, Yasuo
Publicado 2020

TBX5 R264K acts as a modifier to develop dilated cardiomyopathy in mice independently of T-box pathway

por Miyao, Nariaki, Hata, Yukiko, Izumi, Hironori, Nagaoka, Ryo, Oku, Yuko, Takasaki, Ichiro, Ishikawa, Taisuke, Takarada, Shinya, Okabe, Mako, Nakaoka, Hideyuki, Ibuki, Keijiro, Ozawa, Sayaka, Yoshida, Tomoyuki, Hasegawa, Hideyuki, Makita, Naomasa, Nishida, Naoki, Mori, Hisashi, Ichida, Fukiko, Hirono, Keiichi
Publicado 2020

Fibrosis, Connexin-43, and Conduction Abnormalities in the Brugada Syndrome

por Nademanee, Koonlawee, Raju, Hariharan, de Noronha, Sofia V., Papadakis, Michael, Robinson, Laurence, Rothery, Stephen, Makita, Naomasa, Kowase, Shinya, Boonmee, Nakorn, Vitayakritsirikul, Vorapot, Ratanarapee, Samrerng, Sharma, Sanjay, van der Wal, Allard C., Christiansen, Michael, Tan, Hanno L., Wilde, Arthur A., Nogami, Akihiko, Sheppard, Mary N., Veerakul, Gumpanart, Behr, Elijah R.
Publicado 2015

Embryonic type Na(+) channel β-subunit, SCN3B masks the disease phenotype of Brugada syndrome

por Okata, Shinichiro, Yuasa, Shinsuke, Suzuki, Tomoyuki, Ito, Shogo, Makita, Naomasa, Yoshida, Tetsu, Li, Min, Kurokawa, Junko, Seki, Tomohisa, Egashira, Toru, Aizawa, Yoshiyasu, Kodaira, Masaki, Motoda, Chikaaki, Yozu, Gakuto, Shimojima, Masaya, Hayashiji, Nozomi, Hashimoto, Hisayuki, Kuroda, Yusuke, Tanaka, Atsushi, Murata, Mitsushige, Aiba, Takeshi, Shimizu, Wataru, Horie, Minoru, Kamiya, Kaichiro, Furukawa, Tetsushi, Fukuda, Keiichi
Publicado 2016

Flecainide ameliorates arrhythmogenicity through NCX flux in Andersen-Tawil syndrome-iPS cell-derived cardiomyocytes

por Kuroda, Yusuke, Yuasa, Shinsuke, Watanabe, Yasuhide, Ito, Shogo, Egashira, Toru, Seki, Tomohisa, Hattori, Tetsuhisa, Ohno, Seiko, Kodaira, Masaki, Suzuki, Tomoyuki, Hashimoto, Hisayuki, Okata, Shinichiro, Tanaka, Atsushi, Aizawa, Yoshiyasu, Murata, Mitsushige, Aiba, Takeshi, Makita, Naomasa, Furukawa, Tetsushi, Shimizu, Wataru, Kodama, Itsuo, Ogawa, Satoshi, Kokubun, Norito, Horigome, Hitoshi, Horie, Minoru, Kamiya, Kaichiro, Fukuda, Keiichi
Publicado 2017

A Nonsynonymous Polymorphism in Semaphorin 3A as a Risk Factor for Human Unexplained Cardiac Arrest with Documented Ventricular Fibrillation

por Nakano, Yukiko, Chayama, Kazuaki, Ochi, Hidenori, Toshishige, Masaaki, Hayashida, Yasufumi, Miki, Daiki, Hayes, C. Nelson, Suzuki, Hidekazu, Tokuyama, Takehito, Oda, Noboru, Suenari, Kazuyoshi, Uchimura-Makita, Yuko, Kajihara, Kenta, Sairaku, Akinori, Motoda, Chikaaki, Fujiwara, Mai, Watanabe, Yoshikazu, Yoshida, Yukihiko, Ohkubo, Kimie, Watanabe, Ichiro, Nogami, Akihiko, Hasegawa, Kanae, Watanabe, Hiroshi, Endo, Naoto, Aiba, Takeshi, Shimizu, Wataru, Ohno, Seiko, Horie, Minoru, Arihiro, Koji, Tashiro, Satoshi, Makita, Naomasa, Kihara, Yasuki
Publicado 2013

Targeted deep sequencing analyses of long QT syndrome in a Japanese population

por Nagata, Yuki, Watanabe, Ryo, Eichhorn, Christian, Ohno, Seiko, Aiba, Takeshi, Ishikawa, Taisuke, Nakano, Yukiko, Aizawa, Yoshiyasu, Hayashi, Kenshi, Murakoshi, Nobuyuki, Nakajima, Tadashi, Yagihara, Nobue, Mishima, Hiroyuki, Sudo, Takeaki, Higuchi, Chihiro, Takahashi, Atsushi, Sekine, Akihiro, Makiyama, Takeru, Tanaka, Yoshihiro, Watanabe, Atsuyuki, Tachibana, Motomi, Morita, Hiroshi, Yoshiura, Koh-ichiro, Tsunoda, Tatsuhiko, Watanabe, Hiroshi, Kurabayashi, Masahiko, Nogami, Akihiko, Kihara, Yasuki, Horie, Minoru, Shimizu, Wataru, Makita, Naomasa, Tanaka, Toshihiro
Publicado 2022

Variants in the SCN5A Promoter Associated With Various Arrhythmia Phenotypes

por Yagihara, Nobue, Watanabe, Hiroshi, Barnett, Phil, Duboscq‐Bidot, Laetitia, Thomas, Atack C., Yang, Ping, Ohno, Seiko, Hasegawa, Kanae, Kuwano, Ryozo, Chatel, Stéphanie, Redon, Richard, Schott, Jean‐Jacques, Probst, Vincent, Koopmann, Tamara T., Bezzina, Connie R., Wilde, Arthur A. M., Nakano, Yukiko, Aiba, Takeshi, Miyamoto, Yoshihiro, Kamakura, Shiro, Darbar, Dawood, Donahue, Brian S., Shigemizu, Daichi, Tanaka, Toshihiro, Tsunoda, Tatsuhiko, Suda, Masayoshi, Sato, Akinori, Minamino, Tohru, Endo, Naoto, Shimizu, Wataru, Horie, Minoru, Roden, Dan M., Makita, Naomasa
Publicado 2016

SCN5A Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in SCN5A Families

por Wijeyeratne, Yanushi D., Tanck, Michael W., Mizusawa, Yuka, Batchvarov, Velislav, Barc, Julien, Crotti, Lia, Bos, J. Martijn, Tester, David J., Muir, Alison, Veltmann, Christian, Ohno, Seiko, Page, Stephen P., Galvin, Joseph, Tadros, Rafik, Muggenthaler, Martina, Raju, Hariharan, Denjoy, Isabelle, Schott, Jean-Jacques, Gourraud, Jean-Baptiste, Skoric-Milosavljevic, Doris, Nannenberg, Eline A., Redon, Richard, Papadakis, Michael, Kyndt, Florence, Dagradi, Federica, Castelletti, Silvia, Torchio, Margherita, Meitinger, Thomas, Lichtner, Peter, Ishikawa, Taisuke, Wilde, Arthur A.M., Takahashi, Kazuhiro, Sharma, Sanjay, Roden, Dan M., Borggrefe, Martin M., McKeown, Pascal P., Shimizu, Wataru, Horie, Minoru, Makita, Naomasa, Aiba, Takeshi, Ackerman, Michael J., Schwartz, Peter J., Probst, Vincent, Bezzina, Connie R., Behr, Elijah R.
Publicado 2020

European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement...

por Wilde, Arthur A. M., Semsarian, Christopher, Márquez, Manlio F., Sepehri Shamloo, Alireza, Ackerman, Michael J., Ashley, Euan A., Sternick Eduardo, Back, Barajas‐Martinez, Héctor, Behr, Elijah R., Bezzina, Connie R., Breckpot, Jeroen, Charron, Philippe, Chockalingam, Priya, Crotti, Lia, Gollob, Michael H., Lubitz, Steven, Makita, Naomasa, Ohno, Seiko, Ortiz‐Genga, Martín, Sacilotto, Luciana, Schulze‐Bahr, Eric, Shimizu, Wataru, Sotoodehnia, Nona, Tadros, Rafik, Ware, James S., Winlaw, David S., Kaufman, Elizabeth S., Aiba, Takeshi, Bollmann, Andreas, Choi, Jong‐Il, Dalal, Aarti, Darrieux, Francisco, Giudicessi, John, Guerchicoff, Mariana, Hong, Kui, Krahn, Andrew D., Mac Intyre, Ciorsti, Mackall, Judith A., Mont, Lluís, Napolitano, Carlo, Ochoa Juan, Pablo, Peichl, Petr, Pereira, Alexandre C., Schwartz, Peter J., Skinner, Jon, Stellbrink, Christoph, Tfelt‐Hansen, Jacob, Deneke, Thomas
Publicado 2022

European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement...

por Wilde, Arthur A M, Semsarian, Christopher, Márquez, Manlio F, Shamloo, Alireza Sepehri, Ackerman, Michael J, Ashley, Euan A, Sternick, Eduardo Back, Barajas-Martinez, Héctor, Behr, Elijah R, Bezzina, Connie R, Breckpot, Jeroen, Charron, Philippe, Chockalingam, Priya, Crotti, Lia, Gollob, Michael H, Lubitz, Steven, Makita, Naomasa, Ohno, Seiko, Ortiz-Genga, Martín, Sacilotto, Luciana, Schulze-Bahr, Eric, Shimizu, Wataru, Sotoodehnia, Nona, Tadros, Rafik, Ware, James S, Winlaw, David S, Kaufman, Elizabeth S, Aiba, Takeshi, Bollmann, Andreas, Choi, Jong Il, Dalal, Aarti, Darrieux, Francisco, Giudicessi, John, Guerchicoff, Mariana, Hong, Kui, Krahn, Andrew D, MacIntyre, Ciorsti, Mackall, Judith A, Mont, Lluís, Napolitano, Carlo, Ochoa, Juan Pablo, Peichl, Petr, Pereira, Alexandre C, Schwartz, Peter J, Skinner, Jon, Stellbrink, Christoph, Tfelt-Hansen, Jacob, Deneke, Thomas
Publicado 2022

Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry

por Crotti, Lia, Spazzolini, Carla, Nyegaard, Mette, Overgaard, Michael T, Kotta, Maria-Christina, Dagradi, Federica, Sala, Luca, Aiba, Takeshi, Ayers, Mark D, Baban, Anwar, Barc, Julien, Beach, Cheyenne M, Behr, Elijah R, Bos, J Martijn, Cerrone, Marina, Covi, Peter, Cuneo, Bettina, Denjoy, Isabelle, Donner, Birgit, Elbert, Adrienne, Eliasson, Håkan, Etheridge, Susan P, Fukuyama, Megumi, Girolami, Francesca, Hamilton, Robert, Horie, Minoru, Iascone, Maria, Jaimez, Juan Jiménez, Jensen, Henrik Kjærulf, Kannankeril, Prince J, Kaski, Juan P, Makita, Naomasa, Muñoz-Esparza, Carmen, Odland, Hans H, Ohno, Seiko, Papagiannis, John, Porretta, Alessandra Pia, Prandstetter, Christopher, Probst, Vincent, Robyns, Tomas, Rosenthal, Eric, Rosés-Noguer, Ferran, Sekarski, Nicole, Singh, Anoop, Spentzou, Georgia, Stute, Fridrike, Tfelt-Hansen, Jacob, Till, Jan, Tobert, Kathryn E, Vinocur, Jeffrey M, Webster, Gregory, Wilde, Arthur A M, Wolf, Cordula M, Ackerman, Michael J, Schwartz, Peter J
Publicado 2023

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 2020