Literature DB >> 8747872

Spastic paraparesis and mutations in the prion protein gene.

M Yamada1, S Satoh, N Sodeyama, H Fujigasaki, K Kaneko, Y Wada, Y Itoh, M Matsushita.   

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Year:  1995        PMID： 8747872     DOI： 10.1016/0022-510x(95)00250-4

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN： 0022-510X            Impact factor:   3.181


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  4 in total

1.  Involvement of the peripheral nervous system in human prion diseases including dural graft associated Creutzfeldt-Jakob disease.

Authors:  C Ishida; S Okino; T Kitamoto; M Yamada
Journal:  J Neurol Neurosurg Psychiatry       Date:  2005-03       Impact factor: 10.154

2.  Frontal lobe dementia with abnormal cholesterol metabolism and heterozygous mutation in sterol 27-hydroxylase gene (CYP27).

Authors:  S Sugama; A Kimura; W Chen; S Kubota; Y Seyama; N Taira; Y Eto
Journal:  J Inherit Metab Dis       Date:  2001-06       Impact factor: 4.982

3.  An autopsy report of three kindred in a Gerstmann-Sträussler-Scheinker disease P105L family with a special reference to prion protein, tau, and beta-amyloid.

Authors:  Keisuke Ishizawa; Takashi Mitsufuji; Kei Shioda; Atsushi Kobayashi; Takashi Komori; Yoshihiko Nakazato; Tetsuyuki Kitamoto; Nobuo Araki; Toshimasa Yamamoto; Atsushi Sasaki
Journal:  Brain Behav       Date:  2018-09-21       Impact factor: 2.708

4.  A patient with spastic paralysis finally diagnosed as V180I genetic Creutzfeldt-Jakob disease 9 years after onset.

Authors:  Taichi Nomura; Ikuko Iwata; Ryoji Naganuma; Masaaki Matsushima; Katsuya Satoh; Tetsuyuki Kitamoto; Ichiro Yabe
Journal:  Prion       Date:  2020-12       Impact factor: 3.931
  4 in total

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