The main goal of the Pilot Projects Program is to provide a flexible and efficient means for initiating novel clinical research projects in a timely manner. The two main objectives are to encourage the development of smaller projects to the point where they can be published, or they can compete for independent funding. A third objective is to stimulate collaboration, both among investigators of the Dystonia Coalition, and outside investigators. Priority is given to projects that are short (<2 years), have modest budgets (usually less than $50,000/yr), have clear and direct relevance to dystonia, optimally leverage the resources of the Dystonia Coalition, and maximize the likelihood of development into larger independently-funded projects or publications with high impact. The process is initiated by a request for applications that is distributed to all members of the Dystonia Coalition at least yearly, and to each of our Patient Advocacy Groups (PAGs) for further distribution. Eligible projects may come from investigators both within and outside the Dystonia Coalition. All pilot projects must have a direct clinical or translational focus; purely basic science proposals are not accepted. All projects are reviewed by a committee that includes Dystonia Coalition investigators, representatives from at least one PAG, and the NIH. The program has a yearly budget of at least $50,000 to support 1-2 projects yearly. These funds are augmented by one or more Dystonia PAGs, depending on availability of funds and their special interests in the types of projects received. As an example of the operation of our Pilot Projects Program and its remarkable success, a list of previously supported Pilot Projects and their outcomes is provided, along with details regarding their co- sponsorship with one or more PAGs.
| Scorr, Laura M; Silver, Michael R; Hanfelt, John et al. (2018) Pilot Single-Blind Trial of AbobotulinumtoxinA in Oromandibular Dystonia. Neurotherapeutics 15:452-458 |
| Morris, Aimee E; Norris, Scott A; Perlmutter, Joel S et al. (2018) Quantitative, clinically relevant acoustic measurements of focal embouchure dystonia. Mov Disord 33:449-458 |
| Jinnah, H A; Hess, Ellen J (2018) Evolving concepts in the pathogenesis of dystonia. Parkinsonism Relat Disord 46 Suppl 1:S62-S65 |
| Cotton, Adam C; Bell, R B; Jinnah, H A (2018) Expert Opinion vs Patient Perspective in Treatment of Rare Disorders: Tooth Removal in Lesch-Nyhan Disease as an Example. JIMD Rep 41:25-27 |
| Jinnah, H A; Comella, Cynthia L; Perlmutter, Joel et al. (2018) Longitudinal studies of botulinum toxin in cervical dystonia: Why do patients discontinue therapy? Toxicon 147:89-95 |
| Jinnah, H A; Albanese, Alberto; Bhatia, Kailash P et al. (2018) Treatable inherited rare movement disorders. Mov Disord 33:21-35 |
| Shi, Lucy L; Simpson, C Blake; Hapner, Edie R et al. (2018) Pharyngeal Dystonia Mimicking Spasmodic Dysphonia. J Voice 32:234-238 |
| Liu, Hui; Jin, Hongjun; Luo, Zonghua et al. (2018) In Vivo Characterization of Two 18F-Labeled PDE10A PET Radioligands in Nonhuman Primate Brains. ACS Chem Neurosci 9:1066-1073 |
| Defazio, Giovanni; Hallett, Mark; Jinnah, Hyder A et al. (2017) Blepharospasm 40 years later. Mov Disord 32:498-509 |
| Shaikh, Aasef G; Ghasia, Fatema F (2017) Novel Eye Movement Disorders in Whipple's Disease-Staircase Horizontal Saccades, Gaze-Evoked Nystagmus, and Esotropia. Front Neurol 8:321 |
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