Your browser doesn't support javascript.
loading
Autosomal-recessive complicated spastic paraplegia with a novel lysosomal trafficking regulator gene mutation.
Shimazaki, Haruo; Honda, Junko; Naoi, Tametou; Namekawa, Michito; Nakano, Imaharu; Yazaki, Masahide; Nakamura, Katsuya; Yoshida, Kunihiro; Ikeda, Shu-ichi; Ishiura, Hiroyuki; Fukuda, Yoko; Takahashi, Yuji; Goto, Jun; Tsuji, Shoji; Takiyama, Yoshihisa.
Afiliação
  • Shimazaki H; Division of Neurology, Department of Internal Medicine, Jichi Medical University School of Medicine, Tochigi, Japan.
  • Honda J; Division of Neurology, Department of Internal Medicine, Jichi Medical University School of Medicine, Tochigi, Japan.
  • Naoi T; Division of Neurology, Department of Internal Medicine, Jichi Medical University School of Medicine, Tochigi, Japan.
  • Namekawa M; Division of Neurology, Department of Internal Medicine, Jichi Medical University School of Medicine, Tochigi, Japan.
  • Nakano I; Department of Neurology, Tokyo Metropolitan Neurological Hospital, Tokyo, Japan.
  • Yazaki M; Department of Medicine (Neurology and Rheumatology), Shinshu University School of Medicine, Nagano, Japan.
  • Nakamura K; Department of Medicine (Neurology and Rheumatology), Shinshu University School of Medicine, Nagano, Japan.
  • Yoshida K; Department of Medicine (Neurology and Rheumatology), Shinshu University School of Medicine, Nagano, Japan.
  • Ikeda S; Department of Medicine (Neurology and Rheumatology), Shinshu University School of Medicine, Nagano, Japan.
  • Ishiura H; Department of Neurology, Graduate School of Medicine, University of Tokyo, Tokyo, Japan.
  • Fukuda Y; Department of Neurology, Graduate School of Medicine, University of Tokyo, Tokyo, Japan.
  • Takahashi Y; Department of Neurology, Graduate School of Medicine, University of Tokyo, Tokyo, Japan.
  • Goto J; Department of Neurology, Graduate School of Medicine, University of Tokyo, Tokyo, Japan.
  • Tsuji S; Department of Neurology, Graduate School of Medicine, University of Tokyo, Tokyo, Japan.
  • Takiyama Y; Department of Neurology, Interdisciplinary Graduate School of Medicine and Engineering, University of Yamanashi, Yamanashi, Japan.
J Neurol Neurosurg Psychiatry ; 85(9): 1024-8, 2014 Sep.
Article em En | MEDLINE | ID: mdl-24521565

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Paraplegia Espástica Hereditária / Síndrome de Chediak-Higashi / Proteínas de Transporte Vesicular Tipo de estudo: Prognostic_studies Limite: Humans / Male / Middle aged Idioma: En Revista: J Neurol Neurosurg Psychiatry Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Paraplegia Espástica Hereditária / Síndrome de Chediak-Higashi / Proteínas de Transporte Vesicular Tipo de estudo: Prognostic_studies Limite: Humans / Male / Middle aged Idioma: En Revista: J Neurol Neurosurg Psychiatry Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Japão