Zobrazeno 1 - 10 of 12 pro vyhledávání: '"Kazuo Mutsukura"'
1
[A case of secondary central nervous system lymphoma presenting marked hypoglycorrhachia]
Autor: Masahiro Tokuda, Kazuo Mutsukura, Masatoshi Matsuo, Aya Yamashita, Yohei Tateishi, Junji Irie
Publikováno v: Rinsho shinkeigaku = Clinical neurology. 59(6)
A 67-year-old male was transferred to our hospital with diplopia, decreased deep tendon reflex and ataxia. He had been suspected Fisher syndrome because of previous upper respiratory tract infection. A cerebrospinal fluid examination showed marked hy
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90e8e79089c8945bfec23ade15993542
https://pubmed.ncbi.nlm.nih.gov/31142712
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2
Iatrogenic Removal of the Intima in the Middle Cerebral Artery by a Stent Retriever: A Report of Two Cases
Autor: Susumu Yamaguchi, Nobuhiro Yagi, Aya Yamashita, Nobutaka Horie, Junpei Hamabe, Kazuo Mutsukura, Kazuhiko Suyama, Junji Irie, Yoshihiro Tokuda
Publikováno v: World neurosurgery. 118
Background Mechanical thrombectomy improves functional outcomes in patients with acute ischemic stroke. However, stent retrievers have the risk of vascular damage. Case Description We present 2 cases of patients with acute internal carotid artery occ
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08c65cf8e4e88119279722dbc96cf454
https://pubmed.ncbi.nlm.nih.gov/30048785
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3
Establishment of a standard 14-3-3 protein assay of cerebrospinal fluid as a diagnostic tool for Creutzfeldt–Jakob disease
Autor: Minoru Tobiume, Susumu Shirabe, Yusei Shiga, Katsuya Satoh, Kazuo Mutsukura, Katsumi Eguhchi, Noriyuki Nishida, Testutaro Sata, Yuki Matsui
Publikováno v: Laboratory Investigation. 90:1637-1644
Periodic sharp wave complexes observed on an electroencephalographic recording and the presence of a 14-3-3 protein in the cerebrospinal fluid (CSF) are both included in the diagnostic criteria for the Creutzfeldt-Jakob disease (CJD) supplied by the
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a23f7a64426348f132d318304b63b1b5
https://doi.org/10.1038/labinvest.2009.68
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4
Development of an Ultra-Rapid Diagnostic Method Based on Heart-Type Fatty Acid Binding Protein Levels in the CSF of CJD Patients
Autor: Yasufumi Kataoka, Kazuo Mutsukura, Katsumi Eguchi, Hideo Matsuda, Takuya Watanabe, Masaichi Sugino, Katsuya Satoh, Susumu Shirabe, Noriyuki Nishida, Yuki Matsui
Publikováno v: Cellular and molecular neurobiology. 30(7):991-999
Creutzfeldt-Jakob disease (CJD) is a transmissible, fatal, neurodegenerative disease in humans. Recently, various drugs have been reported to be useful in the treatment of CJD; however, for such treatments to be useful it is essential to rapidly and
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2da23a8404a5e93ce5ca81465845bee
https://nagasaki-u.repo.nii.ac.jp/records/15320
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5
Familial Creutzfeldt-Jakob disease with a V180I mutation: comparative analysis with pathological findings and diffusion-weighted images
Autor: Tetsuyuki Kitamoto, Kensuke Sasaki, Katsumi Eguchi, Susumu Shirabe, Minoru Morikawa, Katsuya Satoh, Kazuo Mutsukura, Yusei Shiaga, Itsuro Tomita, Takayasu Fukutome, Masachika Iseki
Publikováno v: Dementia and geriatric cognitive disorders. 28(6):550-557
BACKGROUND: Diffusion-weighted imaging (DWI) has been reported to be a useful technique for diagnosing Creutzfeldt-Jakob disease (CJD). The present study reported DWI results in cases of familial CJD with a V180I mutation (CJD180) in the prion protei
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11f9825cf90e60caf844719ca18f7071
http://hdl.handle.net/10069/23204
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7
Successful Treatment of a Patient with Primary Sjoegren's Syndrome Complicated with Pericarditis during Pregnancy
Autor: Katsumi Eguchi, Atsushi Kawakami, Hideki Nakamura, Nozomi Iwanaga, Kazuo Mutsukura, Masako Furuyama, Hiroaki Ida, Tomoki Origuchi
Publikováno v: Internal Medicine. 46:1143-1147
A 35-year-old woman with primary Sjogren's syndrome (pSS) developed fever and chest pain during pregnancy. When the dose of prednisolone was reduced, she experienced chest pain with elevated CRP and D-dimer, resulting in admission to our hospital wit
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba0c4c6d37fb0af34fee01be433ebc03
https://doi.org/10.2169/internalmedicine.46.0062
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8
Acute motor sensory axonal neuropathy associated with Henoch-Schönlein purpura
Autor: Hirosato Inoue, Kazuo Mutsukura, Shinsuke Fujioka, Fujio Fujiki, Yoshio Tsuboi, Tatsuo Yamada
Publikováno v: Journal of the neurological sciences. 263(1-2)
A 41-year-old man was admitted with progressive tetraparesis with hypoesthesia. He also presented with purpura in both legs. After admission, joint pain, gastrointestinal tract bleeding, and renal dysfunction developed. A nerve conduction study revea
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7009f46109006896fb9b1679e9791cd
https://pubmed.ncbi.nlm.nih.gov/17602705
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9
[Garcin syndrome in a patient with rhinocerebral mucormycosis]
Autor: Kazuo, Mutsukura, Yoshio, Tsuboi, Akiko, Imamura, Fujio, Fujiki, Tatsuo, Yamada
Publikováno v: No to shinkei = Brain and nerve. 56(3)
Garcin syndrome is characterized by an unilateral cranial nerves involvement without sensory or motor long-tract disturbances. It is usually caused by tumor infiltrating in the skull base with osteolytic changes on radiological study. We report a cas
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::77a9ff5e8dd83e2bbfeda4a541db28f6
https://pubmed.ncbi.nlm.nih.gov/15112447
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10
[Cheiromegaly and podomegaly associated with primary progressive multiple sclerosis: a case report]
Autor: Kazuo, Mutsukura, Shinji, Ouma, Shinji, Sakata, Masashi, Nakajima, Yoshio, Tsuboi, Tatsuo, Yamada
Publikováno v: No to shinkei = Brain and nerve. 55(12)
Cheiromegaly is an extremely rare syndrome characterized by unilateral hand hypertrophy with hyperhydrosis. Unilateral foot hypertrophy has been described as podomegaly. Cheiromegaly/podomegaly is usually seen in patients with syringomyelia. Although
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::241ad465bd37b5b20771f3959eeba164
https://pubmed.ncbi.nlm.nih.gov/14870575
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