Lewis Sudarsky
Affiliations: | Harvard Medical School, Boston, MA, United States |
Google:
"Lewis Sudarsky"Mean distance: (not calculated yet)
BETA: Related publications
See more...
Publications
|
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
| Chou KL, Elm JJ, Wielinski CL, et al. (2017) Factors associated with falling in early, treated Parkinson's disease: The NET-PD LS1 cohort. Journal of the Neurological Sciences. 377: 137-143 |
| Taylor KM, Saint-Hilaire MH, Sudarsky L, et al. (2015) Head injury at early ages is associated with risk of Parkinson's disease. Parkinsonism & Related Disorders |
| Locascio JJ, Eberly S, Liao Z, et al. (2015) Association between α-synuclein blood transcripts and early, neuroimaging-supported Parkinson's disease. Brain : a Journal of Neurology. 138: 2659-71 |
| Kieburtz K, Tilley BC, et al. (2015) Effect of creatine monohydrate on clinical progression in patients with Parkinson disease: a randomized clinical trial. Jama. 313: 584-93 |
| Parashos SA, Elm J, Boyd JT, et al. (2015) Validation of an ambulatory capacity measure in Parkinson disease: a construct derived from the Unified Parkinson's Disease Rating Scale. Journal of Parkinson's Disease. 5: 67-73 |
| Ding H, Dhima K, Lockhart KC, et al. (2013) Unrecognized vitamin D3 deficiency is common in Parkinson disease: Harvard Biomarker Study. Neurology. 81: 1531-7 |
| Viswanathan A, Sudarsky L. (2012) Balance and gait problems in the elderly. Handbook of Clinical Neurology. 103: 623-34 |
| Ding H, Sarokhan AK, Roderick SS, et al. (2011) Association of SNCA with Parkinson: replication in the Harvard NeuroDiscovery Center Biomarker Study. Movement Disorders : Official Journal of the Movement Disorder Society. 26: 2283-6 |
| Nichols WC, Marek DK, Pauciulo MW, et al. (2007) R1514Q substitution in Lrrk2 is not a pathogenic Parkinson's disease mutation Movement Disorders. 22: 254-257 |
| Pankratz N, Pauciulo MW, Elsaesser VE, et al. (2006) Mutations in LRRK2 other than G2019S are rare in a north-American based sample of familial Parkinson's didease Movement Disorders. 21: 2257-2260 |