Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Takashi Irioka"'
Autor:
Kokoro Ozaki, Takashi Irioka, Toshiki Uchihara, Akane Yamada, Ayako Nakamura, Takamasa Majima, Susumu Igarashi, Hiroshi Shintaku, Mayumi Yakeishi, Yukio Tsuura, Yasushi Okazaki, Kinya Ishikawa, Takanori Yokota
Publikováno v:
Acta Neuropathologica Communications, Vol 9, Iss 1, Pp 1-16 (2021)
Abstract Spinocerebellar ataxia type 34 (SCA34) is an autosomal dominant inherited ataxia due to mutations in ELOVL4, which encodes one of the very long-chain fatty acid elongases. SCA38, another spinocerebellar ataxia, is caused by mutations in ELOV
Externí odkaz:
https://doaj.org/article/97ed9ae073614bd38dd9f013f3bd258e
Autor:
Michael Winklehner, Jan Bauer, Verena Endmayr, Carmen Schwaiger, Gerda Ricken, Masakatsu Motomura, Shunsuke Yoshimura, Hiroshi Shintaku, Kinya Ishikawa, Yukio Tsuura, Takahiro Iizuka, Takanori Yokota, Takashi Irioka, Romana Höftberger
Publikováno v:
Neurology(R) neuroimmunologyneuroinflammation. 9(4)
Background and ObjectivesParaneoplastic cerebellar degeneration (PCD) is characterized by a widespread loss of Purkinje cells (PCs) and may be associated with autoantibodies against intracellular antigens such as Yo or cell surface neuronal antigens
Autor:
Takamasa Majima, Takashi Irioka, Ayako Nakamura, Yukio Tsuura, Takanori Yokota, Susumu Igarashi, Akane Yamada, Yasushi Okazaki, Mayumi Yakeishi, Kinya Ishikawa, Kokoro Ozaki, Toshiki Uchihara, Hiroshi Shintaku
Publikováno v:
Acta Neuropathologica Communications, Vol 9, Iss 1, Pp 1-16 (2021)
Acta Neuropathologica Communications
Acta Neuropathologica Communications
Spinocerebellar ataxia type 34 (SCA34) is an autosomal dominant inherited ataxia due to mutations in ELOVL4, which encodes one of the very long-chain fatty acid elongases. SCA38, another spinocerebellar ataxia, is caused by mutations in ELOVL5, a gen
Autor:
Takanori Yokota, Eiichiro Amano, Hiroya Kuwahara, Akira Machida, Takashi Irioka, Takuya Ohkubo, Masaki Ohyagi, Yuko K Takahashi, Satoru Ishibashi
Publikováno v:
Internal Medicine
Objective Cryptococcal meningoencephalitis (CM) causes significant morbidity and mortality in human immunodeficiency virus (HIV)-negative and HIV-positive populations. White matter lesions (WMLs) have been reported in both populations of CM patients;
Autor:
Hiroko, Kitanosono, Masakatsu, Motomura, Hiroki, Tomita, Hiroshi, Iwanaga, Naoki, Iwanaga, Takashi, Irioka, Hirokazu, Shiraishi, Akira, Tsujino
Publikováno v:
Brain and nerve = Shinkei kenkyu no shinpo. 71(2)
A 63-year-old female who developed dizziness, diplopia and subsequent gait disturbance from September X-1 year was analyzed. The first neurological findings in May X year revealed cerebellar ataxia, weakness in the proximal limbs, decreased tendon re
Publikováno v:
Journal of Stroke and Cerebrovascular Diseases. 29:105007
Neuromyelitis optica spectrum disorder (NMOSD) is an immune-mediated disorder. It often develops acute myelopathy due to longitudinally extensive transverse myelitis (LETM), although other disorders can cause an LETM-like lesion. Here, we report a 76
Autor:
Kimihiko Kaneko, Tai Otani, Toshiyuki Takahashi, Susumu Igarashi, Takashi Irioka, Takanori Yokota
Publikováno v:
Multiple Sclerosis and Related Disorders. 41:102033
A 22-year-old woman acutely developed recurrent convulsive seizures followed by fever and headache. Cerebrospinal fluid study showed leukocytosis without hypoglycorrhachia. These clinical features suggested acute viral or aseptic encephalitis. The pa
Autor:
Susumu Igarashi, Kazumasa Soga, Takanori Yokota, Takashi Irioka, Kimihiko Kaneko, Tai Otani, Toshiyuki Takahashi, Yuko K Takahashi
Publikováno v:
eNeurologicalSci
Autor:
Josep Dalmau, Lindsey McCracken, Pamela S. Morales, Tania Cellucci, Markus Reindl, Francesc Graus, Maarten J. Titulaer, Frank Leypoldt, Gagandeep Singh, Makito Hirano, Takahiro Iizuka, Huidy Shu, Albert Saiz, Romana Höftberger, Takashi Irioka, Myrna R. Rosenfeld, Leslie Benson, Kenichi Kaida, Alvaro Cobo Calvo, Tomotaka Yamamoto, Paul W. Wirtz
Publikováno v:
Annals of Neurology. 75:411-428
Objective To report the clinical, radiological, and immunological association of demyelinating disorders with anti–N-methyl-D-aspartate receptor (NMDAR) encephalitis. Methods Clinical and radiological analysis was done of a cohort of 691 patients w
Autor:
Yoshiyuki Numasawa, Satoru Ishibashi, Kokoro Ozaki, Takanori Yokota, Takashi Irioka, Mikami Takahisa, Motoki Miura, Yoichiro Nishida
Publikováno v:
Journal of the Neurological Sciences. 392:32-33