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Clinical and pathological findings in familial amyloid polyneuropathy caused by a transthyretin E61K mutation.
Murakami, Tatsufumi; Nishimura, Hirotake; Nagai, Taiji; Hemmi, Shoji; Kutoku, Yumiko; Ohsawa, Yutaka; Sunada, Yoshihide.
Afiliación
  • Murakami T; Department of Neurology, Kawasaki Medical School, 577 Matsushima, Kurashiki, Okayama 701-0192, Japan. Electronic address: tatsum@med.kawasaki-m.ac.jp.
  • Nishimura H; Department of Pathology, Kawasaki Medical School, 577 Matsushima, Kurashiki, Okayama 701-0192, Japan.
  • Nagai T; Department of Neurology, Kawasaki Medical School, 577 Matsushima, Kurashiki, Okayama 701-0192, Japan.
  • Hemmi S; Department of Neurology, Kawasaki Medical School, 577 Matsushima, Kurashiki, Okayama 701-0192, Japan.
  • Kutoku Y; Department of Neurology, Kawasaki Medical School, 577 Matsushima, Kurashiki, Okayama 701-0192, Japan.
  • Ohsawa Y; Department of Neurology, Kawasaki Medical School, 577 Matsushima, Kurashiki, Okayama 701-0192, Japan.
  • Sunada Y; Department of Neurology, Kawasaki Medical School, 577 Matsushima, Kurashiki, Okayama 701-0192, Japan.
J Neurol Sci ; 381: 55-58, 2017 Oct 15.
Article en En | MEDLINE | ID: mdl-28991715
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Prealbúmina / Neuropatías Amiloides Familiares / Mutación Tipo de estudio: Diagnostic_studies Límite: Aged / Female / Humans Idioma: En Revista: J Neurol Sci Año: 2017 Tipo del documento: Article
Texto completo
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XML
PubMed Links
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Prealbúmina / Neuropatías Amiloides Familiares / Mutación Tipo de estudio: Diagnostic_studies Límite: Aged / Female / Humans Idioma: En Revista: J Neurol Sci Año: 2017 Tipo del documento: Article