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135 results

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Page 1
Glucocerebrosidase enzyme activity in GBA mutation Parkinson's disease.
Ortega RA, Torres PA, Swan M, Nichols W, Boschung S, Raymond D, Barrett MJ, Johannes BA, Severt L, Shanker V, Hunt AL, Bressman S, Pastores GM, Saunders-Pullman R. Ortega RA, et al. Among authors: shanker v. J Clin Neurosci. 2016 Jun;28:185-6. doi: 10.1016/j.jocn.2015.12.004. Epub 2016 Feb 5. J Clin Neurosci. 2016. PMID: 26857292 Free PMC article.
Penetrance and expression of dystonia genes.
Saunders-Pullman R, Shriberg J, Shanker V, Bressman SB. Saunders-Pullman R, et al. Among authors: shanker v. Adv Neurol. 2004;94:121-5. Adv Neurol. 2004. PMID: 14509664 Review. No abstract available.
Phenylalanine loading as a diagnostic test for DRD: interpreting the utility of the test.
Saunders-Pullman R, Blau N, Hyland K, Zschocke J, Nygaard T, Raymond D, Shanker V, Mohrmann K, Arnold L, Tabbal S, deLeon D, Ford B, Brin M, Chouinard S, Ozelius L, Klein C, Bressman SB. Saunders-Pullman R, et al. Among authors: shanker v. Mol Genet Metab. 2004 Nov;83(3):207-12. doi: 10.1016/j.ymgme.2004.07.010. Mol Genet Metab. 2004. PMID: 15542391
Narrowing the DYT6 dystonia region and evidence for locus heterogeneity in the Amish-Mennonites.
Saunders-Pullman R, Raymond D, Senthil G, Kramer P, Ohmann E, Deligtisch A, Shanker V, Greene P, Tabamo R, Huang N, Tagliati M, Kavanagh P, Soto-Valencia J, Aguiar Pde C, Risch N, Ozelius L, Bressman S. Saunders-Pullman R, et al. Among authors: shanker v. Am J Med Genet A. 2007 Sep 15;143A(18):2098-105. doi: 10.1002/ajmg.a.31887. Am J Med Genet A. 2007. PMID: 17702011
What's new in dystonia?
Shanker V, Bressman SB. Shanker V, et al. Curr Neurol Neurosci Rep. 2009 Jul;9(4):278-84. doi: 10.1007/s11910-009-0042-5. Curr Neurol Neurosci Rep. 2009. PMID: 19515279 Review.
Gender differences in the risk of familial parkinsonism: beyond LRRK2?
Saunders-Pullman R, Stanley K, San Luciano M, Barrett MJ, Shanker V, Raymond D, Ozelius LJ, Bressman SB. Saunders-Pullman R, et al. Among authors: shanker v. Neurosci Lett. 2011 Jun 1;496(2):125-8. doi: 10.1016/j.neulet.2011.03.098. Epub 2011 Apr 12. Neurosci Lett. 2011. PMID: 21511009 Free PMC article.
Olfactory dysfunction in LRRK2 G2019S mutation carriers.
Saunders-Pullman R, Stanley K, Wang C, San Luciano M, Shanker V, Hunt A, Severt L, Raymond D, Ozelius LJ, Lipton RB, Bressman SB. Saunders-Pullman R, et al. Among authors: shanker v. Neurology. 2011 Jul 26;77(4):319-24. doi: 10.1212/WNL.0b013e318227041c. Epub 2011 Jul 13. Neurology. 2011. PMID: 21753159 Free PMC article.
135 results