Atypical parkinsonism of progressive supranuclear palsy-parkinsonism (PSP-P) phenotype with rare variants in FBXO7 and VPS35 genes associated with Lewy body pathology
Language English Country Germany Media print-electronic
Document type Case Reports, Letter, Research Support, Non-U.S. Gov't
PubMed
30374525
DOI
10.1007/s00401-018-1923-y
PII: 10.1007/s00401-018-1923-y
Knihovny.cz E-resources
- MeSH
- F-Box Proteins genetics MeSH
- Phenotype MeSH
- Lewy Bodies pathology MeSH
- Humans MeSH
- Parkinsonian Disorders diagnosis genetics pathology MeSH
- Supranuclear Palsy, Progressive diagnosis genetics pathology MeSH
- Aged, 80 and over MeSH
- Vesicular Transport Proteins genetics MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Aged, 80 and over MeSH
- Publication type
- Letter MeSH
- Case Reports MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- F-Box Proteins MeSH
- FBXO7 protein, human MeSH Browser
- Vesicular Transport Proteins MeSH
- VPS35 protein, human MeSH Browser
References provided by Crossref.org
Utilizing neurodegenerative markers for the diagnostic evaluation of amyotrophic lateral sclerosis
Endemic parkinsonism: clusters, biology and clinical features
Lewy body disease or diseases with Lewy bodies?
