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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...
Gardado en:
| Publicado en: | J Mov Disord |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
The Korean Movement Disorder Society
2021
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7840237/ https://ncbi.nlm.nih.gov/pubmed/32942840 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.14802/jmd.20060 |
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