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Ira Shoulson

Researcher at Georgetown University

Publications -  40
Citations -  3661

Ira Shoulson is an academic researcher from Georgetown University. The author has contributed to research in topics: Parkinson's disease & Huntington's disease. The author has an hindex of 18, co-authored 40 publications receiving 3239 citations. Previous affiliations of Ira Shoulson include University of Washington & Biogen Idec.

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Levodopa and the progression of Parkinson's disease.

TL;DR: The clinical data suggest that levodopa either slows the progression of Parkinson's disease or has a prolonged effect on the symptoms of the disease, and the neuroimaging data suggest either thatlevodopa accelerates the loss of nigrostriatal dopamine nerve terminals or that its pharmacologic effects modify the dopamine transporter.
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Weight loss in early stage of Huntington’s disease

TL;DR: At an early stage of the disease, subjects with Huntington’s disease had lower body mass index than matched controls from the general population and the parallel to observations in transgenic mouse models suggests that it is a significant hallmark of Huntington's disease gene expression.
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A Randomized Clinical Trial of High-Dosage Coenzyme Q10 in Early Parkinson Disease: No Evidence of Benefit

M. Flint Beal, +160 more
- 01 May 2014 - 
TL;DR: Coenzyme Q10 was safe and well tolerated in this population, but showed no evidence of clinical benefit, and the study was terminated after a prespecified futility criterion was reached.
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Inosine to Increase Serum and Cerebrospinal Fluid Urate in Parkinson Disease: A Randomized Clinical Trial

TL;DR: Inosine was generally safe, tolerable, and effective in raising serum and cerebrospinal fluid urate levels in early PD and support advancing to more definitive development of inosine as a potential disease-modifying therapy for PD.
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Limited Life Expectancy, Human Capital and Health Investments.

TL;DR: This work uses smoking and cancer screening data to test the corollary that health capital responds to life expectancy, and compares investments for individuals who have ex-ante identical risks of HD but differ in disease realization.