Zobrazeno 1 - 10
of 97
pro vyhledávání: '"Mari Iwamoto"'
Autor:
Yasuhiro Ichikawa, Hiroyuki Kuroda, Takeshi Ikegawa, Shun Kawai, Shin Ono, Ki-Sung Kim, Sadamitsu Yanagi, Kenji Kurosawa, Yoko Aoki, Mari Iwamoto, Hideaki Ueda
Publikováno v:
Journal of Cardiovascular Development and Disease, Vol 11, Iss 1, p 10 (2023)
Little information is available on age-related electrocardiographic changes in patients with Noonan syndrome. This single-center study evaluated the electrocardiograms of patients with Noonan syndrome. We divided the patients (n = 112; electrocardiog
Externí odkaz:
https://doaj.org/article/9777c2005b9a4411b03e1db5ba9acdb9
Autor:
Masakatsu Yanagimachi, Sayaka Fukuda, Fumiko Tanaka, Mari Iwamoto, Chiho Takao, Kunihiro Oba, Natsuko Suzuki, Koji Kiyohara, Dai Kuranobu, Norimasa Tada, Ayako Nagashima, Taku Ishii, Yoko Ino, Yayoi Kimura, Nobutoshi Nawa, Takeo Fujiwara, Takuya Naruto, Tomohiro Morio, Shouzaburo Doi, Masaaki Mori
Publikováno v:
PLoS ONE, Vol 16, Iss 9, p e0257138 (2021)
ObjectiveKawasaki disease (KD) is a systemic vasculitis in childhood that can lead to coronary artery lesions (CALs). Although early diagnosis and treatment is important for preventing KD patients from development of CALs, diagnosis depends on the cl
Externí odkaz:
https://doaj.org/article/33fca520da7f4368b4cbbac8e4cb3b0f
Publikováno v:
Allergology International, Vol 52, Iss 4, Pp 219-224 (2003)
Eosinophilic myocarditis is characterized by an acute inflammatory infiltration of eosinophils in the myocardium. Diagnosis is confirmed by a heart muscle biopsy. Immunopathological studies suggest that several toxic proteins, such as eosinophilic ca
Externí odkaz:
https://doaj.org/article/8312f640e6074eb39026013ca92aa483
Publikováno v:
Epilepsy & Seizure. 15:35-41
Autor:
Toshiyuki Shimizu, Shun Kawai, Aiko Kawada, Takuya Wakamiya, Yusuke Nakano, Shigeo Watanabe, Mari Iwamoto
Publikováno v:
Pediatrics International. 65
Autor:
Kei Miyakawa, Mari Iwamoto, Sayaka Fukuda, Takashi Ohya, Mayuko Miyake, Mio Kaneta, Shuichi Ito
Publikováno v:
Modern Rheumatology Case Reports. 5:442-447
The new disease concept of multisystem inflammatory syndrome in children (MIS-C), which is a systemic inflammatory syndrome with multiple organ involvement after SARS-CoV2 infection, was established in 2020. MIS-C is common in Hispanic and black chil
Publikováno v:
Pediatric Cardiology and Cardiac Surgery. 36:334-343
Autor:
Keiichi, Hirono, Nariaki, Miyao, Masao, Yoshinaga, Eiki, Nishihara, Kazushi, Yasuda, Shigeru, Tateno, Mamoru, Ayusawa, Naokata, Sumitomo, Hitoshi, Horigome, Mari, Iwamoto, Hideto, Takahashi, Seiichi, Sato, Shigetoyo, Kogaki, Seiko, Ohno, Tadayoshi, Hata, Daisuke, Hazeki, Naomi, Izumida, Masami, Nagashima, Kunio, Ohta, Nobuo, Tauchi, Hiroya, Ushinohama, Shozaburo, Doi, Fukiko, Ichida, Study group on childhood cardiomyopathy in Japan
Publikováno v:
Epub 2020 Mar 11
Left ventricular noncompaction (LVNC) is a hereditary cardiomyopathy and is associated with high morbidity and mortality. However, the role and significance of school screening for LVNC have not been fully elucidated. In this multicenter, retrospecti
Autor:
Yoshiaki Kato, Naokata Sumitomo, Hiroya Ushinohama, Hideto Takahashi, Masahiro Sonoda, Yuichi Nomura, Norihito Nuruki, Naomi Izumida, Hitoshi Horigome, Seiichi Sato, Tadayoshi Hata, Katsumi Abe, Toshiyuki Chisaka, Tatsuya Yoneyama, Yuji Tanaka, Susumu Hosokawa, Seiko Ohno, Fumie Takechi, Hiromitsu Ogata, Taichi Kato, Tatsunori Hokosaki, Masao Yoshinaga, Kazushi Yasuda, Yumiko Ninomiya, Shigetoyo Kogaki, Takashi Higaki, Eiki Nishihara, Naomasa Makita, Daisuke Hazeki, Kentaro Ueno, Shozaburo Doi, Yoshihiro Nozaki, Keiichi Hirono, Mamoru Ayusawa, Fukiko Ichida, Mari Iwamoto, Minoru Horie, Nobuo Tauchi, Hiroyuki Tsutsui, Akiko Komori, Kunio Ohta, Masami Nagashima, Sigeru Tateno, Satoru Kawai, Yuichi Ishikawa, Shouji Matsushima
Publikováno v:
Circulation journal : official journal of the Japanese Circulation Society. 86(1)
Background The usefulness of electrocardiographic (ECG) voltage criteria for diagnosing hypertrophic cardiomyopathy (HCM) in pediatric patients is poorly defined.Methods and Results:ECGs at the 1st grade (mean [±SD] age 6.6±0.3 years) were availabl
Autor:
Masao Yoshinaga, Tadayosi Hata, Fukiko Ichida, Tomohiko Imamura, Shintaro Nakano, Naokata Sumitomo, Kazushi Yasuda, Seiko Ohno, Hitoshi Horigome, Shigetu Tateno, Shozaburo Doi, Shota Muraji, Eiki Nishihara, Shigetoyo Kogaki, Mari Iwamoto, Masami Nagashima
Publikováno v:
Heart and Vessels.
Restrictive cardiomyopathy (RCM) is a rare myocardial disease with an impaired diastolic function and poor prognosis. Almost all RCM patients are reported to have abnormal P-waves due to atrial overloading. This study aimed to reveal the characterist