Perry Disease: Concept of a New Disease and Clinical Diagnostic Criteria

Perry disease is a hereditary neurodegenerative disease with autosomal dominant inheritance. It is characterized by parkinsonism, psychiatric symptoms, unexpected weight loss, central hypoventilation, and transactive-response DNA-binding protein of 43kD (TDP-43) aggregation in the brain. In 2009, Pe...

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Detalles Bibliográficos
Autores principales: Tsuboi, Yoshio, Mishima, Takayasu, Fujioka, Shinsuke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Movement Disorder Society 2021
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7840237/
https://www.ncbi.nlm.nih.gov/pubmed/32942840
http://dx.doi.org/10.14802/jmd.20060

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7840237/
https://www.ncbi.nlm.nih.gov/pubmed/32942840
http://dx.doi.org/10.14802/jmd.20060

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