Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Misa Matsui"'
Autor:
Shota Kosuge, Yuri Masaoka, Hideyo Kasai, Motoyasu Honma, Kouzou Murakami, Nobuyuki Yoshii, Keiko Watanabe, Takaaki Naito, Miku Kosuge, Misa Matsui, Daiki Shoji, Syunsuke Sakakura, Hidetomo Murakami, Masahiko Izumizaki
Publikováno v:
PLoS ONE, Vol 19, Iss 4 (2024)
Externí odkaz:
https://doaj.org/article/4e3d9caff3b04e2f8ce137933786e1ce
Autor:
Yuri Shimizu, Saburo Sakoda, Misa Matsui, Misaki Yamadera, Masaru Yokoe, Harutoshi Fujimura, Itsuko Nakamichi
Publikováno v:
Neuropathology. 39:404-410
We investigated two autopsy cases of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) using immunohistochemical staining with an anti-mitochondrial antibody against translocase of the outer membrane 20 (TOMM20
Publikováno v:
Rinsho Shinkeigaku.
A Japanese woman first noticed dysarthria at the age of 23. She visited a hospital at the age of 32 and was diagnosed as having myotonic dystrophy clinically. She was diagnosed genetically as having myotonic dystrophy type 1 at 47 years old with 160-
Autor:
Misa Matsui, Harutoshi Fujimura, Toshio Saito, Saburo Sakoda, Tsuyoshi Matsumura, Yuko Iwata, Masanori Asakura
Publikováno v:
Internal Medicine
Objective Heart failure is currently the most serious complication of muscular dystrophy. The transient receptor potential cation channel, subfamily V, member 2 (TRPV2) is a stretch-sensitive Ca channel. In damaged myocytes or cardiomyocytes, TRPV2 t
Autor:
Toshio Saito, Misaki Yamadera, Harutoshi Fujimura, Yasutoshi Koga, Saburo Sakoda, Misa Matsui
Publikováno v:
Neurology and Clinical Neuroscience. 7:344-346
Autor:
Makoto Kinoshita, Misa Matsui, Kei Fukada, Toyoko Matsui, Mitsuru Furuta, Jinichi Sawada, Hideki Mochizuki, Takanori Hazama, Mikito Shimizu, Yuta Kajiyama, Daisuke Hirozawa
Publikováno v:
Journal of Clinical Neurophysiology. 33:564-568
Purpose: Diagnosis of amyotrophic lateral sclerosis (ALS) at an early stage is challenging, thus making the enrollment of these patients in clinical trials infeasible. In this study, we investigated the potential usability of motor unit number index
Autor:
Takashi Hamazaki, Kimiko Inoue, Motomichi Kosuga, Toya Ohashi, Ichizo Nishino, Saburo Sakoda, Tsuyoshi Matsumura, Misa Matsui, Torayuki Okuyama, Yohta Shimada
Publikováno v:
Neurology and Clinical Neuroscience. 5:60-64
Background Pompe disease (PD) is caused by a deficiency of acid alpha-glucosidase (GAA). Its prevalence varies depending on ethnicity and is lower in Japan as compared to other countries. Because of the wide spectrum of clinical features in late onse
Autor:
Misa Matsui, Takuyuki Endo, Chiaki Mori, Yuhei Hasuike, Misaki Yamadera, Michiyo Koroyasu, Saburo Sakoda, Harutoshi Fujimura
Publikováno v:
Medical hypotheses. 134
Intestinal dysbiosis refers to an imbalance in the intestinal flora. The concept of small intestinal bacterial overgrowth (SIBO), a condition of abnormal proliferation of the small intestine microbiota, has been proposed as a form of small intestine
Publikováno v:
Rinsho Shinkeigaku. 56:857-861
A 35-year-old man showed a convulsive attack with consciousness loss and was suspected of having Brugada syndrome 6 months prior to admission to our hospital. At the initial examination, the patient showed conjugate deviation, followed by left limb c
Autor:
Tatsusada Okuno, Hideki Mochizuki, Takanori Hazama, Satoru Tada, Daisuke Hirozawa, Jinichi Sawada, Kei Fukada, Misa Matsui, Mitsuru Furuta, Futoshi Aoike
Publikováno v:
Journal of Neurology, Neurosurgery, and Psychiatry
Anticollapsin response mediator protein 5 antibody (anti-CRMP5 antibody, also known as anti-CV2 antibody) is usually associated with small-cell lung carcinoma (SCLC) or thymoma.1 Although optic neuropathy, cerebellar ataxia and chorea are considered