Zobrazeno 1 - 10
of 64
pro vyhledávání: '"Mitsuru, 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:
Ayumi Matsumoto, Hidetoshi Tsuda, Sadahiro Furui, Masako Kawada‐Nagashima, Tatsuya Anzai, Mitsuru Seki, Kazuhisa Watanabe, Kazuhiro Muramatsu, Hitoshi Osaka, Sadahiko Iwamoto, Ichizo Nishino, Takanori Yamagata
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 9, Pp n/a-n/a (2022)
Abstract Background Actin, alpha, skeletal muscle 1 (ACTA1) is one of the causative genes of nemaline myopathy (NM) and congenital fiber‐type disproportion (CFTD). CFTD is characterized by type 1 fiber atrophy and distinguished from NM in the absen
Externí odkaz:
https://doaj.org/article/107beb8987694f328b4e85f3797128db
Autor:
Saori Fukui, Mitsuru Seki, Takaomi Minami, Kazuhiko Kotani, Kensuke Oka, Akiko Yokomizo, Daisuke Matsubara, Tomoyuki Sato, Yasuyuki Nozaki, Mari Saito, Yutaka Kikuchi, Kenji Miyamoto, Yukifumi Monden, Takanori Yamagata
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 19, Iss 1, Pp 1-7 (2021)
Abstract Background High-dose intravenous immunoglobulin (IVIG) is the mainstay of treatment for Kawasaki disease (KD). Usually, 2 g/kg of IVIG is administered over 10–24 h, depending on the institution or physician, but the association between inf
Externí odkaz:
https://doaj.org/article/a7998922db004aaea3f4525340b037cc
Autor:
Daisuke Matsubara, Daisuke Tamura, Yuka Kasuya, Yoshitaka Mizobe, Mami Hiwada, Mitsuru Seki, Shinji Makino, Takanori Yamagata
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Multisystem inflammatory syndrome in children (MIS-C) is a newly defined hyperinflammatory disease linked to antecedent coronavirus disease 2019. Patients with MIS-C present with various symptoms, and ocular findings such as mild bilateral conjunctiv
Externí odkaz:
https://doaj.org/article/8a6c67d0b9fe493f8d16c72c1b61106f
Autor:
Shun Suzuki, Mitsuru Seki, Koichi Kataoka, Reina Koga, Tomoyuki Sato, Masaaki Kawada, Takanori Yamagata
Publikováno v:
Case Reports in Pediatrics, Vol 2022 (2022)
PHACE syndrome is a congenital disorder often associated with a cervicofacial infantile hemangioma and complicated cardiovascular malformations. Patients with PHACE syndrome often have complex aortic arch anomalies, longer aortic stenosis or agenesis
Externí odkaz:
https://doaj.org/article/16abfa245f1e49528742adb23fd4ec84
Autor:
Mitsuru Seki, Nozomi Furukawa, Norimichi Koitabashi, Masaru Obokata, Simon J Conway, Hirokazu Arakawa, Masahiko Kurabayashi
Publikováno v:
PLoS ONE, Vol 14, Iss 8, p e0220795 (2019)
Transforming growth factor beta (TGF-β) has been shown to play a critical role in pathogenesis of pulmonary arterial hypertension (PAH) although the precise role of TGF-β signaling remains uncertain. A recent report has shown that periostin (Pn) is
Externí odkaz:
https://doaj.org/article/ed327ba5a2ac49868e25db0b09257e19
Autor:
Serguei Ilchenko, Clara Kurishima, Felix Woitek, Mitsuru Seki, Lucia Carlucci, Helen Piontkivska, Takhar Kasumov, Fabio A. Recchia, Gia Burjanadze, Nikoloz Gorgodze, Kenneth Walsh, Ayse Keles, Khatia Gabisonia
Publikováno v:
Journal of Cardiac Failure. 28:588-600
Protein pool turnover is a critically important cellular homeostatic component, yet it has been little explored in the context of heart failure (HF) pathophysiology. We employed in vivo 2H labeling/ proteome dynamics for non-biased discovery of turno
Publikováno v:
The Tohoku Journal of Experimental Medicine. 258:177-182
Autor:
Mitsuru Seki
Kawasaki disease (KD) is a self-limiting vasculitis of unknown etiology primarily affecting young children. The most important aspect in the treatment of KD is the prevention of coronary artery lesions (CALs) because myocardial ischemia or infarction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf5bd902857b72c8c8b0ca0cc51b8621
https://mts.intechopen.com/articles/show/title/cardiovascular-health-in-kawasaki-disease
https://mts.intechopen.com/articles/show/title/cardiovascular-health-in-kawasaki-disease
Autor:
Takanori Yamagata, Mari Saito, Kensuke Oka, Saori Fukui, Tomoyuki Sato, Daisuke Matsubara, Yukifumi Monden, Yasuyuki Nozaki, Kenji Miyamoto, Akiko Yokomizo, Mitsuru Seki, Takaomi Minami, Yutaka Kikuchi, Kazuhiko Kotani
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 19, Iss 1, Pp 1-7 (2021)
Pediatric Rheumatology Online Journal
Pediatric Rheumatology Online Journal
Background High-dose intravenous immunoglobulin (IVIG) is the mainstay of treatment for Kawasaki disease (KD). Usually, 2 g/kg of IVIG is administered over 10–24 h, depending on the institution or physician, but the association between infusion spe