Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Kazuhiro Kurohara"'
Publikováno v:
Journal of the Neurological Sciences. 270:197-200
Marinesco-Sjögren syndrome (MSS) is an autosomal recessive multisystem disorder characterized by cerebellar ataxia, cataracts, progressive muscular weakness, and developmental and mental retardation. Recently, mutations in the SIL1 gene on chromosom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1f58e8f2a869175da918f35d0135cd8
https://doi.org/10.1016/j.jns.2008.02.012
https://doi.org/10.1016/j.jns.2008.02.012
Autor:
Akihiro Sawada, Kazuhiro Kurohara, Makoto Eriguchi, Masashi Nishihara, Akira Uchino, Sho Kudo, Yasuo Kuroda, Y. Takase
Publikováno v:
European Radiology. 15:1701-1704
We report computed tomography (CT) features in a case of segmental thrombosis of the superior sagittal sinus. On the initial cranial CT scan, both frontal cortices showed focal areas of slightly increased attenuation. The lesions were isointense on m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::988c5ef9854c782040f1bd928618d5a0
https://doi.org/10.1007/s00330-004-2440-z
https://doi.org/10.1007/s00330-004-2440-z
Publikováno v:
European Neurology. 41:216-225
The 14-3-3 protein belongs to a family of 30-kD proteins originally identified by two-dimensional analysis of brain protein extracts. Recently, the detection of the 14-3-3 protein in the cerebrospinal fluid (CSF) is utilized as a highly reliable test
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e91fd052728dc85fe70c0dc25b9c412
https://doi.org/10.1159/000008054
https://doi.org/10.1159/000008054
Autor:
Shigeru Katamine, Noriyuki Nishida, Tsutomu Miyamoto, Motohiro Yukitake, Kazuhiro Kurohara, Jun-ichi Satoh, Yasuo Kuroda
Publikováno v:
Experimental Neurology. 151:105-115
Recent evidence has suggested that molecular chaperones participate in the conformational change between the normal cellular prion protein (PrPC) and its scrapie isoform (PrPSc). To study a role of PrPC in the regulation of expression of heat shock p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27bae3ab902804e999db154c5bc8db3b
https://doi.org/10.1006/exnr.1998.6796
https://doi.org/10.1006/exnr.1998.6796
Publikováno v:
Journal of the Neurological Sciences. 155:170-177
Interleukin-15 (IL-15) is a novel cytokine which shares activities and receptor components with IL-2. To investigate the biological roles of IL-15 in the human nervous system, we examined the expression of mRNAs for IL-15 and the IL-15 receptor three
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98b0ae93d75080d7b92ba2d0839cac3f
https://doi.org/10.1016/s0022-510x(97)00310-9
https://doi.org/10.1016/s0022-510x(97)00310-9
Autor:
T. Yamamoto, Yasuo Kuroda, Y. Kukita, H. Tokumoto, Jun-ichi Satoh, Makoto Matsui, K. Hayashi, Motohiro Yukitake, Hirokazu Furuya, Kazuhiro Kurohara, N. Shinnoh, Takuro Kobayashi
Publikováno v:
Neurology. 49:1392-1399
A 51-year-old woman developed a slowly progressive spastic paraparesis and diminished vibration sense beginning at age 38. Intellectual capacity was normal. Krabbe disease was confirmed by markedly reduced leukocyte galactocerebrosidase (GALC) activi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::feb57c32d400c48c59a37856eb2c2a8a
https://doi.org/10.1212/wnl.49.5.1392
https://doi.org/10.1212/wnl.49.5.1392
Publikováno v:
Neuropathology. 17:80-88
The expression of mRNAs for neurotrophins and neurotrophin receptors was examined in NTera2/cl.D1 (NT2) human embryonal carcinoma cells at various stages of retinoic acid (RA)-induced neuronal differentiation using reverse transcription-polymerase ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14926498671917ef0324c9664a64fc29
https://doi.org/10.1111/j.1440-1789.1997.tb00018.x
https://doi.org/10.1111/j.1440-1789.1997.tb00018.x
Publikováno v:
Journal of Neuroimmunology. 45:133-136
Based on our previous finding of elevated interferon-gamma levels in the cerebrospinal fluid (CSF), but not in serum, of HTLV-I-associated myelopathy (HAM), we assayed serum and CSF levels of granulocyte-macrophage colony-stimulating factor (GM-CSF),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b872694724be779b4845b27c01f3543a
https://doi.org/10.1016/0165-5728(93)90173-v
https://doi.org/10.1016/0165-5728(93)90173-v
Autor:
Yasuo Kuroda, Ryusuke Kakigi, Hiroshi Takashima, Ryuji Neshige, Chiyoko Endo, Fumino Fujiyama, Kazuhiro Kurohara, Makoto Matsui
Publikováno v:
Acta Neurologica Scandinavica. 86:82-86
Treatment with interferon-alpha (IFN-alpha) was undertaken in 16 patients with human T-lymphotropic virus type I-associated myelopathy (HAM). All patients had progressive spastic paraparesis before treatment. Twelve patients were enrolled in an open
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a2de33ce1998af3562f09f878b1b3d9
https://doi.org/10.1111/j.1600-0404.1992.tb08059.x
https://doi.org/10.1111/j.1600-0404.1992.tb08059.x
Autor:
Hiroyuki Onoue, Yasuo Kuroda, Haruo Mizuta, Yusuke Yakushiji, Kazuhiro Kurohara, Ryuichiro Okada, Toshiro Yoshimura
Publikováno v:
Archives of neurology. 64(5)
Objective To report the clinical, pathological, and mutational features of hereditary C1 inhibitor (C1INH) deficiency as a cause of isolated vasculitic neuropathy. Patient A 35-year-old woman with sensorimotor mononeuritis multiplex and facial palsy.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::880af65681883e2c449b994672ce0c43
https://pubmed.ncbi.nlm.nih.gov/17502473
https://pubmed.ncbi.nlm.nih.gov/17502473