Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

279 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Nonmotor symptoms in healthy Ashkenazi Jewish carriers of the G2019S mutation in the LRRK2 gene.
Mirelman A, Alcalay RN, Saunders-Pullman R, Yasinovsky K, Thaler A, Gurevich T, Mejia-Santana H, Raymond D, Gana-Weisz M, Bar-Shira A, Ozelius L, Clark L, Orr-Urtreger A, Bressman S, Marder K, Giladi N; LRRK2 AJ consortium. Mirelman A, et al. Among authors: bressman s. Mov Disord. 2015 Jun;30(7):981-6. doi: 10.1002/mds.26213. Epub 2015 Mar 21. Mov Disord. 2015. PMID: 25809001 Free PMC article.
The effect of estrogen replacement on early Parkinson's disease.
Saunders-Pullman R, Gordon-Elliott J, Parides M, Fahn S, Saunders HR, Bressman S. Saunders-Pullman R, et al. Among authors: bressman s. Neurology. 1999 Apr 22;52(7):1417-21. doi: 10.1212/wnl.52.7.1417. Neurology. 1999. PMID: 10227628
Pediatric movement disorders.
Saunders-Pullman R, Braun I, Bressman S. Saunders-Pullman R, et al. Among authors: bressman s. Child Adolesc Psychiatr Clin N Am. 1999 Oct;8(4):747-65, viii. Child Adolesc Psychiatr Clin N Am. 1999. PMID: 10553201 Review.
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.
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.
Distribution, type, and origin of Parkin mutations: review and case studies.
Hedrich K, Eskelson C, Wilmot B, Marder K, Harris J, Garrels J, Meija-Santana H, Vieregge P, Jacobs H, Bressman SB, Lang AE, Kann M, Abbruzzese G, Martinelli P, Schwinger E, Ozelius LJ, Pramstaller PP, Klein C, Kramer P. Hedrich K, et al. Mov Disord. 2004 Oct;19(10):1146-57. doi: 10.1002/mds.20234. Mov Disord. 2004. PMID: 15390068 Review.
LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews.
Ozelius LJ, Senthil G, Saunders-Pullman R, Ohmann E, Deligtisch A, Tagliati M, Hunt AL, Klein C, Henick B, Hailpern SM, Lipton RB, Soto-Valencia J, Risch N, Bressman SB. Ozelius LJ, et al. N Engl J Med. 2006 Jan 26;354(4):424-5. doi: 10.1056/NEJMc055509. N Engl J Med. 2006. PMID: 16436782 No abstract available.
The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 gene.
Brashear A, Dobyns WB, de Carvalho Aguiar P, Borg M, Frijns CJ, Gollamudi S, Green A, Guimaraes J, Haake BC, Klein C, Linazasoro G, Münchau A, Raymond D, Riley D, Saunders-Pullman R, Tijssen MA, Webb D, Zaremba J, Bressman SB, Ozelius LJ. Brashear A, et al. Among authors: bressman sb. Brain. 2007 Mar;130(Pt 3):828-35. doi: 10.1093/brain/awl340. Epub 2007 Feb 4. Brain. 2007. PMID: 17282997
279 results