Slow disease progression and characteristic TDP-43 inclusions in a patient with familial amyotrophic lateral sclerosis carrying a TARDBP G357S variant.

Sainouchi, Makoto; Oginezawa, Shinya; Tada, Mari; Ishihara, Tomohiko; Onodera, Osamu; Kakita, Akiyoshi

Sainouchi, Makoto; Oginezawa, Shinya; Tada, Mari; Ishihara, Tomohiko; Onodera, Osamu; Kakita, Akiyoshi.

Sainouchi M; Department of Pathology, Brain Research Institute, Niigata University, Niigata, Japan.
Oginezawa S; Department of Neurology, Brain Research Institute, Niigata University, Niigata, Japan.
Tada M; Department of Pathology, Brain Research Institute, Niigata University, Niigata, Japan.
Ishihara T; Department of Neurology, Brain Research Institute, Niigata University, Niigata, Japan.
Onodera O; Advanced Treatment of Neurological Diseases Branch, Endowed Research Branch, Brain Research Institute, Niigata University, Niigata, Japan.
Kakita A; Department of Neurology, Brain Research Institute, Niigata University, Niigata, Japan.

Neuropathol Appl Neurobiol ; 50(1): e12966, 2024 Feb.

Article en En | MEDLINE | ID: mdl-38389123

Asunto(s)

Esclerosis Amiotrófica Lateral; Humanos; Esclerosis Amiotrófica Lateral/genética; Progresión de la Enfermedad; Proteínas de Unión al ADN/genética; Mutación

Palabras clave

TARDBP; TDP-43; amyotrophic lateral sclerosis; astrocytic inclusions; neuropathology

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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Esclerosis Amiotrófica Lateral Límite: Humans Idioma: En Año: 2024 Tipo del documento: Article

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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Esclerosis Amiotrófica Lateral Límite: Humans Idioma: En Año: 2024 Tipo del documento: Article