ロード中...
Quantitative, functional MRI and neurophysiological markers in a case of Gerstmann-Sträussler-Scheinker syndrome
Gerstmann-Sträussler-Scheinker syndrome (GSS) is an inherited autosomal dominant prion disease, caused by a codon 102 proline to leucine substitution (P102L) in the prion protein gene (PRNP). We describe the case of a 40-year-old male, affected by a slowly progressive gait disturbance, leg weakness...
保存先:
| 出版年: | Funct Neurol |
|---|---|
| 主要な著者: | , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
CIC Edizioni Internazionali
2017
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5726351/ https://ncbi.nlm.nih.gov/pubmed/29042004 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.11138/FNeur/2017.32.3.153 |
| タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|