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The wide-ranging clinical and genetic features in Japanese families with valosin-containing protein proteinopathy.
Ando, Takashi; Nakamura, Ryoichi; Kuru, Satoshi; Yokoi, Daichi; Atsuta, Naoki; Koike, Haruki; Suzuki, Masashi; Hara, Kazuhiro; Iguchi, Yohei; Harada, Yumiko; Yoshida, Yusuke; Hattori, Makoto; Murakami, Ayuka; Noda, Seiya; Kimura, Seigo; Sone, Jun; Nakamura, Tomohiko; Goto, Yoji; Mano, Kazuo; Okada, Hisashi; Okuda, Satoshi; Nishino, Ichizo; Ogi, Tomoo; Sobue, Gen; Katsuno, Masahisa.
Afiliación
  • Ando T; Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan.
  • Nakamura R; Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan.
  • Kuru S; Department of Neurology, National Hospital Organization Suzuka National Hospital, Suzuka, Mie, Japan.
  • Yokoi D; Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan; Department of Neurology, Kakeyu-Misayama Rehabilitation Center Kakeyu Hospital, Ueda, Nagano, Japan.
  • Atsuta N; Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan.
  • Koike H; Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan.
  • Suzuki M; Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan.
  • Hara K; Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan.
  • Iguchi Y; Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan.
  • Harada Y; Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan.
  • Yoshida Y; Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan.
  • Hattori M; Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan.
  • Murakami A; Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan; Department of Neurology, National Hospital Organization Suzuka National Hospital, Suzuka, Mie, Japan.
  • Noda S; Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan; Department of Neurology, National Hospital Organization Suzuka National Hospital, Suzuka, Mie, Japan.
  • Kimura S; Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan; Department of Neurology, National Hospital Organization Suzuka National Hospital, Suzuka, Mie, Japan.
  • Sone J; Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan; Department of Neurology, National Hospital Organization Suzuka National Hospital, Suzuka, Mie, Japan.
  • Nakamura T; Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan.
  • Goto Y; Department of Neurology, Japanese Red Cross Nagoya Daiichi Hospital, Nagoya, Aichi, Japan.
  • Mano K; Department of Neurology, Japanese Red Cross Nagoya Daiichi Hospital, Nagoya, Aichi, Japan.
  • Okada H; Department of Neurology, National Hospital Organization Nagoya Medical Center, Nagoya, Aichi, Japan.
  • Okuda S; Department of Neurology, National Hospital Organization Nagoya Medical Center, Nagoya, Aichi, Japan.
  • Nishino I; Department of Neuromuscular Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Tokyo, Japan.
  • Ogi T; Department of Genetics, Research Institute of Environmental Medicine (RIeM), Nagoya University, Nagoya, Aichi, Japan.
  • Sobue G; Brain and Mind Research Center, Nagoya University, Nagoya, Aichi, Japan.
  • Katsuno M; Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan. Electronic address: ka2no@med.nagoya-u.ac.jp.
Neurobiol Aging ; 100: 120.e1-120.e6, 2021 04.
Article en En | MEDLINE | ID: mdl-33339634
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Polineuropatías / Enfermedades Desmielinizantes / Miositis por Cuerpos de Inclusión / Mutación Missense / Proteína que Contiene Valosina / Esclerosis Amiotrófica Lateral Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adult / Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Neurobiol Aging Año: 2021 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Estados Unidos
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Polineuropatías / Enfermedades Desmielinizantes / Miositis por Cuerpos de Inclusión / Mutación Missense / Proteína que Contiene Valosina / Esclerosis Amiotrófica Lateral Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adult / Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Neurobiol Aging Año: 2021 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Estados Unidos