Physician perceptions of pharmacologic treatment options for chorea associated with Huntington disease in the United States
Author:
Affiliation:
1. University of Alabama School of Medicine, Birmingham, AL, USA;
2. Teva Pharmaceutical Industries, Frazer, PA, USA;
3. Ipsos Healthcare, San Francisco, CA, USA;
4. Vanderbilt University Medical Center, Nashville, TN, USA
Funder
Teva Pharmaceutical Industries, Petach Tikva, Israel
Publisher
Informa UK Limited
Subject
General Medicine
Link
https://www.tandfonline.com/doi/pdf/10.1080/03007995.2018.1435518
Reference18 articles.
1. HDSA. What is HD? 2016. Available at: http://hdsa.org/what-is-hd/ [Last accessed 26 September 2017]
2. Genetic and clinical peculiarities in a new family with hereditary hypophosphatemic rickets with hypercalciuria: a case report
3. Targets for future clinical trials in Huntington's disease: What's in the pipeline?
4. The incidence and prevalence of Huntington's disease: A systematic review and meta-analysis
5. Identification of health-related quality of life (HRQOL) issues relevant to individuals with Huntington disease
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2. The Many Faces of Huntington’s Chorea Treatment: The Impact of Sudden Withdrawal of Tiapride after 40 Years of Use and a Systematic Review;Journal of Personalized Medicine;2022-04-06
3. An MDS Evidence‐Based Review on Treatments for Huntington's Disease;Movement Disorders;2021-11-29
4. State-of-the-art pharmacological approaches to reduce chorea in Huntington’s disease;Expert Opinion on Pharmacotherapy;2021-02-08
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