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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. 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.
Pediatric movement disorders.
Saunders-Pullman R, Braun I, Bressman S. Saunders-Pullman R, et al. Child Adolesc Psychiatr Clin N Am. 1999 Oct;8(4):747-65, viii. Child Adolesc Psychiatr Clin N Am. 1999. PMID: 10553201 Review.
Localization of a gene for myoclonus-dystonia to chromosome 7q21-q31.
Nygaard TG, Raymond D, Chen C, Nishino I, Greene PE, Jennings D, Heiman GA, Klein C, Saunders-Pullman RJ, Kramer P, Ozelius LJ, Bressman SB. Nygaard TG, et al. Ann Neurol. 1999 Nov;46(5):794-8. doi: 10.1002/1531-8249(199911)46:5<794::aid-ana19>3.0.co;2-2. Ann Neurol. 1999. PMID: 10554001
Inherited myoclonus-dystonia.
Saunders-Pullman R, Ozelius L, Bressman SB. Saunders-Pullman R, et al. Adv Neurol. 2002;89:185-91. Adv Neurol. 2002. PMID: 11968443 Review. No abstract available.
Diagnostic criteria for dystonia in DYT1 families.
Bressman SB, Raymond D, Wendt K, Saunders-Pullman R, De Leon D, Fahn S, Ozelius L, Risch N. Bressman SB, et al. Neurology. 2002 Dec 10;59(11):1780-2. doi: 10.1212/01.wnl.0000035630.12515.e0. Neurology. 2002. PMID: 12473770 Clinical Trial.
Penetrance and expression of dystonia genes.
Saunders-Pullman R, Shriberg J, Shanker V, Bressman SB. Saunders-Pullman R, et al. Adv Neurol. 2004;94:121-5. Adv Neurol. 2004. PMID: 14509664 Review. No abstract available.
173 results