Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Taro Kitamura"'
Autor:
Yuya Kano, Kentaro Yamada, Masahiro Muto, Shingo Inaguma, Mari Yoshida, Taro Kitamura, Toshiyasu Miura, Hiroki Nakanishi, Yusuke Mori, Shingo Murakami, Noriyuki Matsukawa
Publikováno v:
Neurology and Clinical Neuroscience. 10:183-185
Publikováno v:
Rinsho Shinkeigaku. 59:814-817
An 86-year-old woman was admitted to our hospital with headache and acute detarioration of consciousness. Cerebral microbleeds (CMBs) dominated the occipital lobe on the head MRI, revealing white matter lesions. It was accompanied by gadolinium (Gd)
Publikováno v:
Rinsho shinkeigaku = Clinical neurology. 61(4)
A 78-year-old woman was diagnosed with herpes zoster in the first branch of the trigeminal nerve and was treated with amenamevir. Subsequently, she was hospitalized for postherpetic neuralgia. Fever and unconsciousness were observed, and a diagnosis
Publikováno v:
Rinsho shinkeigaku = Clinical neurology. 60(9)
A 23-year-old man admitted to our hospital with headache and dysarthria. Head MRI showed multiple acute cerebral infarctions in the right posterior circulation. Atlantoaxial dislocation, atlas dysplasia and thrombotic occlusion of right vertebral art
Autor:
Chikako Sato, Yuto Uchida, Taro Kitamura, Noriyuki Matsukawa, Masahiro Muto, Hiroyasu Inoue, Yuya Kano, Toshiyasu Miura, Kentaro Yamada, Keita Sakurai
Publikováno v:
Journal of Stroke and Cerebrovascular Diseases. 31:106178
Bow hunter's syndrome is the mechanical compression of the vertebral artery due to cervical rotation, resulting in ischemic symptoms in the vertebrobasilar artery territory. However, some cases present without typical symptoms and exhibit compression
Publikováno v:
Rinsho Shinkeigaku. 58:202-205
Cerebrospinal fluid leakage can develop due to traffic trauma or lumbar puncture; however, in many cases, it develops spontaneously without any obvious cause. This report describes a case of cerebrospinal fluid leakage caused by bowling activity. A 5
Autor:
Takuya Miyabayashi, Hiroshi Oba, Sato Suzuki-Muromoto, Yukimune Okubo, Mai Anzai, Wakaba Endo, Noriko Togashi, Naomichi Matsumoto, Hirotomo Saitsu, Taro Kitamura, Kazuhiro Haginoya, Takehiko Inui, Yusuke Takezawa
Publikováno v:
Brain and Development. 39:873-876
We report a patient with Muenke syndrome who had repetitive apneic spell followed by focal status epilepticus in the early infancy. Ictal EEG showed focal spikes bursts originated from the left hemisphere and sifted to the right hemisphere, during wh
Autor:
Taro Kitamura, Toshihiro Ohura, Takashi Uchida, Yurika Numata, Toshiyuki Nishio, Kazuhiro Haginoya, Wakaba Endo, Masaru Takayanagi
Publikováno v:
Pediatrics International. 58:750-753
Acute encephalitis with refractory, repetitive partial seizures (AERRPS) is characterized by repetitive seizures during the acute and chronic phases and has a poor neurological outcome. Burst-suppression coma via continuous i.v. infusion of a short-a
Autor:
Hirotomo Saitsu, Taro Kitamura, Takehiko Inui, Tomohiro Kaneta, Naomi Hino-Fukuyo, Noriko Miyake, Shigeo Kure, Naomichi Matsumoto, Mai Anzai, Yusuke Takezawa, Mitsugu Uematsu, Noriko Togashi, Yukimune Okubo, Tomoko Kobayashi, Kauzhiro Haginoya, Wakaba Endo
Publikováno v:
Journal of the Neurological Sciences. 362:309-313
We conducted a [(18)F]fluorodeoxyglucose positron emission tomography (FDG-PET) study in five patients (median age 11 (range 4-13) years) with Leigh syndrome to evaluate its usefulness for understanding the functional brain dysfunction in this diseas
Autor:
Hirofumi Kodera, Noriko Miyake, Akihiko Ishiyama, Kosuke Kohashi, Atsuo Kikuchi, Taro Kitamura, Mitsuhiro Kato, Hirotaka Motoi, Saoko Takeshita, Kazuhiro Haginoya, Yoshinori Tsurusaki, Toshiyuki Maeda, Naomi Hino-Fukuyo, Naomichi Matsumoto, Muneaki Matsuo, Mitsuko Nakashima, Chihiro Ohba, Daisuke Tajima, Hirotomo Saitsu, Kaoru Araki, Masayuki Sasaki, Shigeo Kure
Publikováno v:
Epilepsia. 57:566-573
SummaryObjective GABRA1 mutations have been identified in patients with familial juvenile myoclonic epilepsy, sporadic childhood absence epilepsy, and idiopathic familial generalized epilepsy. In addition, de novo GABRA1 mutations were recently repor