Effective follow-up care for patients with Parkinson's disease (PD) and their families
integrates clinical care of the motor and non-motor symptoms with a referral process
for physical therapy and for addressing occupational and social issues, particularly
safety issues about the home. To aid this follow up, it would be helpful to have a
concise reference of community-based resources from which selected information can
be provided to patients during their clinical visits. A reference guide of this sort
(Table 1) will be of particular help to clinicians without access to the ancillary support
services found at a university or major medical center.
Table 1Care Resources in the United States for Patients with Parkinsonism.
Keywords
To read this article in full you will need to make a payment
Purchase one-time access:
Academic & Personal: 24 hour online accessCorporate R&D Professionals: 24 hour online accessOne-time access price info
- For academic or personal research use, select 'Academic and Personal'
- For corporate R&D use, select 'Corporate R&D Professionals'
Subscribe:
Subscribe to Journal of the Neurological SciencesAlready a print subscriber? Claim online access
Already an online subscriber? Sign in
Register: Create an account
Institutional Access: Sign in to ScienceDirect
Article info
Publication history
Published online: November 23, 2022
Accepted:
November 21,
2022
Received in revised form:
November 15,
2022
Received:
October 4,
2022
Identification
Copyright
© 2022 Elsevier B.V. All rights reserved.
