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839 results

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Page 1
Parkinson disease phenotype in Ashkenazi Jews with and without LRRK2 G2019S mutations.
Alcalay RN, Mirelman A, Saunders-Pullman R, Tang MX, Mejia Santana H, Raymond D, Roos E, Orbe-Reilly M, Gurevich T, Bar Shira A, Gana Weisz M, Yasinovsky K, Zalis M, Thaler A, Deik A, Barrett MJ, Cabassa J, Groves M, Hunt AL, Lubarr N, San Luciano M, Miravite J, Palmese C, Sachdev R, Sarva H, Severt L, Shanker V, Swan MC, Soto-Valencia J, Johannes B, Ortega R, Fahn S, Cote L, Waters C, Mazzoni P, Ford B, Louis E, Levy O, Rosado L, Ruiz D, Dorovski T, Pauciulo M, Nichols W, Orr-Urtreger A, Ozelius L, Clark L, Giladi N, Bressman S, Marder KS. Alcalay RN, et al. Among authors: ford b. Mov Disord. 2013 Dec;28(14):1966-71. doi: 10.1002/mds.25647. Epub 2013 Oct 15. Mov Disord. 2013. PMID: 24243757 Free PMC article.
Parkinsonism, dystonia, and hemiatrophy.
Greene PE, Bressman SB, Ford B, Hyland K. Greene PE, et al. Among authors: ford b. Mov Disord. 2000 May;15(3):537-41. doi: 10.1002/1531-8257(200005)15:3<537::AID-MDS1018>3.0.CO;2-3. Mov Disord. 2000. PMID: 10830421
The natural history of embouchure dystonia.
Frucht SJ, Fahn S, Greene PE, O'Brien C, Gelb M, Truong DD, Welsh J, Factor S, Ford B. Frucht SJ, et al. Among authors: ford b. Mov Disord. 2001 Sep;16(5):899-906. doi: 10.1002/mds.1167. Mov Disord. 2001. PMID: 11746620
Glucocerebrosidase activity in Parkinson's disease with and without GBA mutations.
Alcalay RN, Levy OA, Waters CC, Fahn S, Ford B, Kuo SH, Mazzoni P, Pauciulo MW, Nichols WC, Gan-Or Z, Rouleau GA, Chung WK, Wolf P, Oliva P, Keutzer J, Marder K, Zhang X. Alcalay RN, et al. Among authors: ford b. Brain. 2015 Sep;138(Pt 9):2648-58. doi: 10.1093/brain/awv179. Epub 2015 Jun 27. Brain. 2015. PMID: 26117366 Free PMC article.
Nonsteroidal Anti-inflammatory Use and LRRK2 Parkinson's Disease Penetrance.
San Luciano M, Tanner CM, Meng C, Marras C, Goldman SM, Lang AE, Tolosa E, Schüle B, Langston JW, Brice A, Corvol JC, Goldwurm S, Klein C, Brockman S, Berg D, Brockmann K, Ferreira JJ, Tazir M, Mellick GD, Sue CM, Hasegawa K, Tan EK, Bressman S, Saunders-Pullman R; Michael J. Fox Foundation LRRK2 Cohort Consortium. San Luciano M, et al. Mov Disord. 2020 Oct;35(10):1755-1764. doi: 10.1002/mds.28189. Epub 2020 Jul 14. Mov Disord. 2020. PMID: 32662532 Free PMC article.
Oral and genital tardive pain syndromes.
Ford B, Greene P, Fahn S. Ford B, et al. Neurology. 1994 Nov;44(11):2115-9. doi: 10.1212/wnl.44.11.2115. Neurology. 1994. PMID: 7969969
SCARB2 variants and glucocerebrosidase activity in Parkinson's disease.
Alcalay RN, Levy OA, Wolf P, Oliva P, Zhang XK, Waters CH, Fahn S, Kang U, Liong C, Ford B, Mazzoni P, Kuo S, Johnson A, Xiong L, Rouleau GA, Chung W, Marder KS, Gan-Or Z. Alcalay RN, et al. Among authors: ford b. NPJ Parkinsons Dis. 2016;2:16004-. doi: 10.1038/npjparkd.2016.4. Epub 2016 Mar 10. NPJ Parkinsons Dis. 2016. PMID: 27110593 Free PMC article.
Delayed-onset cerebellar syndrome.
Louis ED, Lynch T, Ford B, Greene P, Bressman SB, Fahn S. Louis ED, et al. Among authors: ford b. Arch Neurol. 1996 May;53(5):450-4. doi: 10.1001/archneur.1996.00550050080027. Arch Neurol. 1996. PMID: 8624221
839 results