Zobrazeno 1 - 10
of 269
pro vyhledávání: '"Imaharu Nakano"'
Autor:
Kenji Ishihara, Hiroo Ichikawa, Yoshio Suzuki, Jun’ichi Shiota, Imaharu Nakano, Mitsuru Kawamura
Publikováno v:
Behavioural Neurology, Vol 23, Iss 3, Pp 153-158 (2010)
Agraphia, as a neuropsychological symptom of ALS, especially ALS with dementia (ALS-D), has recently attracted more attention. However, the brain lesion responsible has not been identified. Here we present an autopsy case of ALS-D of a patient with o
Externí odkaz:
https://doaj.org/article/a1afd62a0e7642658bcc880e9883e17b
Publikováno v:
Neurology Research International, Vol 2011 (2011)
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder, and the majority of ALS are sporadic (SALS). Recently, several causative genes for familial ALS (FALS) were identified, but the cause of the SALS is still unknown. This
Externí odkaz:
https://doaj.org/article/f74cfd60612e488ea0546145a47b6339
Autor:
Tsuyoshi Okuno, Takashi Nakayama, Nae Konishi, Hideo Michibata, Koji Wakimoto, Yutaka Suzuki, Shinji Nito, Toshio Inaba, Imaharu Nakano, Shin-Ichi Muramatsu, Makoto Takano, Yasushi Kondo, Nobuo Inoue
Publikováno v:
PLoS ONE, Vol 4, Iss 7, p e6318 (2009)
BACKGROUND: Neurons and glial cells can be efficiently induced from mouse embryonic stem (ES) cells in a conditioned medium collected from rat primary-cultured astrocytes (P-ACM). However, the use of rodent primary cells for clinical applications may
Externí odkaz:
https://doaj.org/article/0f6941e750db407e9280ea0f11740c53
Publikováno v:
Neuropathology : official journal of the Japanese Society of NeuropathologyREFERENCES.
Here, we describe two patients who presented with focal cortical signs and underwent neuropathological examination. Case 1 was a 73-year-old woman with progressive speech disorder and abnormal behavior. She showed agraphia of the frontal lobe type, f
Autor:
Kazuhiko Watabe, Eiji Isozaki, Akihiro Kawata, Imaharu Nakano, Kazuhiro Imamura, Toshio Shimizu, Kota Bokuda, Masaharu Hayashi, Yuki Nakayama
Publikováno v:
Muscle & Nerve. 54:277-283
Introduction: This study aimed to determine the prognostic factors and the values that predict survival after percutaneous endoscopic gastrostomy (PEG) tube placement in patients with amyotrophic lateral sclerosis (ALS). Methods: We retrospectively a
Autor:
Koichi Kondo, Shiro Matsubara, Akihiro Kawata, Imaharu Nakano, Takashi Komori, Kazuhito Miyamoto
Publikováno v:
Clinical and Experimental Neuroimmunology. 7:185-196
Objective Morphological analyses to assess the integrity of myonuclear surface structures in muscle biopsies from patients with inclusion body myositis (IBM) and related disorders were carried out to find clues to the causes of IBM. Methods Muscle bi
Publikováno v:
Journal of Integrative Neuroscience, Vol 19, Iss 1, Pp 125-129 (2020)
Autosomal recessive cerebellar ataxias comprise many types of diseases. The most frequent autosomal recessive cerebellar ataxias are Friedreich ataxia, but other types are relatively rare. We encountered a consanguineous family with two cases of late
Autor:
Mikio Sawada, Tohru Matsuura, Takashi Sakatani, Imaharu Nakano, Noriyoshi Fukushima, Hiroki Imada
Publikováno v:
Pathology International. 65:549-553
Rosai-Dorfman disease (RDD) is a benign histiocytic proliferative disorder characterized by the accumulation of histiocytes in lymph nodes and various other organs. RDD seldom involves the central nervous system, and cases of purely intracranial RDD
Autor:
Yuki Nakayama, Kentaro Hayashi, Toshio Shimizu, Chiharu Matsuda, Eiji Isozaki, Yoko Mochizuki, Imaharu Nakano, Kiyomitsu Oyanagi, Akihiro Kawata, Masahiro Nagao, Kazuhiko Watabe
Publikováno v:
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 17:38-46
Predictors of communication impairment in patients with amyotrophic lateral sclerosis (ALS) using tracheostomy-invasive ventilation (TIV) were investigated. Seventy-six ALS patients using TIV were enrolled and classified into three subgroups of commu
Autor:
Yu-ichi Goto, Masako Mukai, Kota Bokuda, Keizo Sugaya, Tadashi Ozawa, Shiro Matsubara, Akira Yagishita, Akinori Miyakoshi, Imaharu Nakano
Publikováno v:
Neurology and Clinical Neuroscience. 3:153-156
Stroke-like episode represents a clinical hallmark of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes. Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes are usually suspected based on