Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Futoshi Aoike"'
Autor:
Jo Matsuzaki, Yasuko Sugiyama, Natsuki Tanaka, Fukuko Nishida, Shoichi Shiraishi, Takehiko Yanagihara, Tomoko Yoshida, Tomomi Enami, Shintaro Sugiyama, Emi Kitamura, Futoshi Aoike, Yoshinobu Okuda
Publikováno v:
Restorative Neurology and Neuroscience. 39:139-147
Background: Functional recoveries after rehabilitation of patients with branch atheromatous disease (BAD) have not been well investigated, however, clinical category of cerebral infarction including BAD itself could be a potential predictive factor f
Autor:
Yoshinobu Okuda, Futoshi Aoike
Publikováno v:
International journal of rehabilitation research. Internationale Zeitschrift fur Rehabilitationsforschung. Revue internationale de recherches de readaptation. 44(3)
To investigate potential differences in functional recovery after rehabilitation between intracerebral haemorrhage and cerebral infarction, we retrospectively compared the outcomes of patients with intracerebral haemorrhage (N = 208) and cerebral inf
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
Autor:
Kei Fukada, Yuta Kajiyama, Mikito Shimizu, Takanori Hazama, Daisuke Hirozawa, Futoshi Aoike, Jinichi Sawada, Taku Hoshi
Publikováno v:
Nosotchu. 35:30-35
Autor:
Ryogen Sasaki, Masanori P. Takahashi, Kazuhiko Hirose, Masanobu Kinoshita, Tomoya Kubota, Futoshi Aoike, Saburo Sakoda
Publikováno v:
Muscle & Nerve. 39:666-673
Myotonia manifests in several hereditary diseases, including hyperkalemic periodic paralysis (HyperPP), paramyotonia congenita (PMC), and potassium-aggravated myotonia (PAM). These are allelic disorders originating from missense mutations in the gene
Publikováno v:
The Japanese Journal of Rehabilitation Medicine. 44:40-45
Cerebral venous thrombosis(CVT)is a rare cerebrovascular disorder. However, many reports have suggested that the prognosis of CVT is better than arterial ischemic infarction accompanied with cytotoxic edema. In this report, we present three cases of
Autor:
Tomoya, Kubota, Masanobu, Kinoshita, Ryogen, Sasaki, Futoshi, Aoike, Masanori P, Takahashi, Saburo, Sakoda, Kazuhiko, Hirose
Publikováno v:
Musclenerve. 39(5)
Myotonia manifests in several hereditary diseases, including hyperkalemic periodic paralysis (HyperPP), paramyotonia congenita (PMC), and potassium-aggravated myotonia (PAM). These are allelic disorders originating from missense mutations in the gene
Publikováno v:
European journal of pharmacology. 532(1-2)
Flecainide, a class Ic antiarrhythmic drug, has been anecdotally reported to improve myotonia, but little is known about its kinetics on human skeletal muscle sodium channels applicable in vivo. Here we explored the anti-myotonic action of flecainide
Autor:
Masayuki Nakamori, Saburo Sakoda, Angela F. Dulhunty, Takashi Kimura, Harutoshi Fujimura, Robert T. Dirksen, John D. Lueck, Futoshi Aoike, Masanori P. Takahashi, Pierre Pouliquin
Publikováno v:
Human molecular genetics. 14(15)
Myotonic dystrophy type 1 (DM1) is a debilitating multisystemic disorder caused by a CTG repeat expansion in the DMPKgene. Aberrant splicing of several genes has been reported to contribute to some symptoms of DM1, but the cause of muscle weakness in
Autor:
Satoru Tada, Mitsuru Furuta, Kei Fukada, Daisuke Hirozawa, Misa Matsui, Futoshi Aoike, Tatsusada Okuno, Jin-ichi Sawada, Hideki Mochizuki, Takanori Hazama, Tada, Satoru, Furuta, Mitsuru, Fukada, Kei, Hirozawa, Daisuke, Matsui, Misa, Aoike, Futoshi, Okuno, Tatsusada, Sawada, Jin-Ichi, Mochizuki, Hideki, Hazama, Takanori
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry; Aug2016, Vol. 87 Issue 8, p907-910, 4p, 1 Color Photograph