Zobrazeno 1 - 10
of 58
pro vyhledávání: '"Shunji, Seki"'
Autor:
Keiichi Hirono, Yukiko Hata, Teruhiko Imamura, Kaori Tsuboi, Shinya Takarada, Mako Okabe, Hideyuki Nakaoka, Keijiro Ibuki, Sayaka Ozawa, Shojiro Ichimata, Naoki Nishida, Hidenori Iwasaki, Susumu Urata, Seigo Okada, Tomoya Hiratsuji, Heima Sakaguchi, Kiyohiro Takigiku, Makoto Nakazawa, Eiki Nishihara, Masako Harada, Osamu Matsuo, Kenji Yasuda, Yoko Yoshida, Hidemasa Namiki, Kazushi Yasuda, Toshinobu Ifuku, Kotaro Urayama, Hideharu Oka, Kayo Ogino, Akio Kato, Nobuhiko Kan, Shunji Seki, Mitsuru Seki, Yutaka Odanaka, Satoru Iwashima, Shuichiro Yoshida, Toyohisa Miyata, Tomoyuki Miyamoto, Ken Watanabe, Naoki Kuwabara, Ryo Inuzuka, Yoshihiro Takahashi, Hisanori Sakazaki, Jun Muneuchi, Shigetoyo Kogaki, Fujito Numano, Sachiko Kido, Masaki Nii, Shinsuke Hoshino, Hidekazu Ishida, Jun Maeda, Yasunobu Hayabuchi, Yoshikazu Otsubo, Kazuyuki Ikeda, Shinya Tsukano, Makoto Watanabe, Nobuo Momoi, Takanari Fujii, Tao Fujioka, Mitsuhiro Fujino, Hiroki Uchiyama, Shigehito Baba, Hitoshi Horigome, Takashi Honda, Kazutaka Suzuki, Fukiko Ichida
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 13, Iss 21 (2024)
Background Left ventricular noncompaction (LVNC) is a hereditary type of cardiomyopathy characterized by prominent trabeculations. Detailed characteristics of biventricular noncompaction (BiVNC) remain unknown. This study aimed to elucidate the clini
Externí odkaz:
https://doaj.org/article/0f80e1600f4e43fb837026a73925f862
Autor:
Shunji Seki, Erika Yamashita, Kazuyuki Tanoue, Norihito Nuruki, Masahiro Sonoda, Seiko Ohno, Hatsue Ishibashi‐Ueda, Yuji Tanaka, Masao Yoshinaga
Publikováno v:
Journal of Arrhythmia, Vol 34, Iss 6, Pp 643-646 (2018)
Abstract We present two cases of biopsy‐proven hypertrophic cardiomyopathy (HCM). Both cases showed abnormal electrocardiographic (ECG) findings more than 8 years before diagnosis. A 16‐year‐old healthy male experienced a rescued cardiac arrest
Externí odkaz:
https://doaj.org/article/c4ab0087dd2b491b9ba0652029476fec
Autor:
Naohiro Ikeda, Shinsuke Maruyama, Kanna Nakano, Ryo Imakiire, Yumiko Ninomiya, Shunji Seki, Kosuke Yanagimoto, Yasuyuki Kakihana, Keiichi Hara, Go Tajima, Yasuhiro Okamoto, Yoshifumi Kawano
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 11, Iss C, Pp 69-71 (2017)
The early-onset form of carnitine palmitoyltransferase (CPT) II deficiency has severe outcomes; patients typically die during the newborn period. We report a case of neonatal-onset CPT II deficiency with prolonged survival, exceeding 24 months. The p
Externí odkaz:
https://doaj.org/article/9145d8919e6d45caa292eac16b0051d8
Autor:
Masao Yoshinaga, Shunji Seki, Norihito Nuruki, Yuji Tanaka, Masahiro Sonoda, Seiko Ohno, Erika Yamashita, Kazuyuki Tanoue, Hatsue Ishibashi‐Ueda
Publikováno v:
Journal of Arrhythmia, Vol 34, Iss 6, Pp 643-646 (2018)
Journal of Arrhythmia
Journal of Arrhythmia
We present two cases of biopsy‐proven hypertrophic cardiomyopathy (HCM). Both cases showed abnormal electrocardiographic (ECG) findings more than 8 years before diagnosis. A 16‐year‐old healthy male experienced a rescued cardiac arrest. Another
Autor:
Yuichi Kodama, Shinsuke Maruyama, Shunji Seki, Manaka Matsunaga, Takayuki Tanabe, Junichiro Nishi, Akinori Miyazono, Michiyoshi Yoshimura, Yoshifumi Kawano
Publikováno v:
Brain and Development. 40:439-442
We report the case of a 12-year-old girl who developed Guillain-Barré syndrome (GBS) and optic neuritis (ON) following Mycoplasma pneumoniae infection. Her symptoms, including bilateral vision impairment and tingling in her hands and right foot, wer
Autor:
Takanari Abematsu, Yasuhiro Okamoto, Akinori Miyazono, Shunsuke Nakagawa, Takuro Nishikawa, Yuichi Shinkoda, Yuichi Kodama, Naohiro Ikeda, Yoshifumi Kawano, Shunji Seki, Hiroyuki Wakiguchi, Koichiro Kurauchi, Takayuki Tanabe
Publikováno v:
Pediatric Transplantation. 20:329-332
Stenotrophomonas maltophilia causes pneumonia and CVC-CRBSI in HSCT. However, there are few reports of pyomyositis due to S. maltophilia. We report a patient with CRBSI and pyomyositis due to S. maltophilia after allogeneic HSCT who was successfully
Publikováno v:
Pediatrics International. 59:1029-1031
Autor:
Kosuke Yanagimoto, Shinsuke Maruyama, Yasuhiro Okamoto, Yasuyuki Kakihana, Naohiro Ikeda, Go Tajima, Ryo Imakiire, Shunji Seki, Yumiko Ninomiya, Yoshifumi Kawano, Kanna Nakano, Keiichi Hara
Publikováno v:
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports, Vol 11, Iss C, Pp 69-71 (2017)
Molecular Genetics and Metabolism Reports, Vol 11, Iss C, Pp 69-71 (2017)
The early-onset form of carnitine palmitoyltransferase (CPT) II deficiency has severe outcomes; patients typically die during the newborn period. We report a case of neonatal-onset CPT II deficiency with prolonged survival, exceeding 24 months. The p
Autor:
Kentaro, Ueno, Shunji, Seki, Naohiro, Shiokawa, Tomoyuki, Matsuba, Akinori, Miyazono, Daisuke, Hazeki, Yutaka, Imoto, Yoshifumi, Kawano
Publikováno v:
Nephrology (Carlton, Vic.). 24(3)
We aimed to validate the incidence of, risk factors for, and postoperative outcomes of acute kidney injury (AKI) according to the modified Kidney Disease Improving Global Outcomes (m-KDIGO) criteria and compare this criteria with both the paediatric
Publikováno v:
Circulation. 136
Background: Few data were available about the QT intervals during nighttime/daytime sleep and daytime activity, and circadian autonomic nerve activities in healthy and LQTS infants. Methods: Holter ECGs were recorded in infants with 12 LQTS infants (