EFNS guidelines on the molecular diagnosis of neurogenetic disorders: general issues, Huntington’s disease, Parkinson’s disease and dystonias
- MeSH Terms
Databases, Bibliographic / statistics & numerical data
Dystonia / diagnosis*
Dystonia / genetics
Genetic Counseling / methods
Guidelines as Topic / standards*
Humans
Huntington Disease / diagnosis*
Huntington Disease / genetics
Molecular Diagnostic Techniques / methods*
Parkinson Disease / diagnosis*
Parkinson Disease / genetics
- Guideline Contact
- Hanne F. Harbo, MD, PhD. Department of Neurology, Ullevål, Oslo University Hospital, 0407 Oslo, Norway (tel.: +47 22118636/+47 99546680; fax: +47 23027455; e-mail: [email protected]/[email protected])
- Publication Date
- 03 June 2009
- Date of Last Evidence Search
- Evidence classification; Experts' recommendations
- Publication Scope
- Diagnosis
- Humans
- Investigation
- Assessment, diagnosis, detection
- Assessment, diagnosis, investigation
- Detection
- Diagnosis
- Diagnostics
- Management
- Countries of Application
- Europe
- Guideline Publication Status
- Published
- Languages
- English
- Authors
- 18
- Willingness to Collaborate
- Yes
