Neb. Rev. Stat. §§ 81-698
Current with changes through the 2024 First Special Legislative Session
The purpose of the Parkinson's Disease Registry is to provide a central data bank of accurate, historical and current information for research purposes. The Parkinson's Disease Registry Act will provide for screening and collecting patient and family data that may be useful in detecting the incidence of and possible risk factors concerning Parkinson's disease and related movement disorders. The act will also aid in planning for health care requirements and education needs.
Neb. Rev. Stat. §§ 81-698