Bressman S - Search Results

1

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.

2

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

3

Evaluation of the role of the D2 dopamine receptor in myoclonus dystonia.

Klein C, Gurvich N, Sena-Esteves M, Bressman S, Brin MF, Ebersole BJ, Fink S, Forsgren L, Friedman J, Grimes D, Holmgren G, Kyllerman M, Lang AE, de Leon D, Leung J, Prioleau C, Raymond D, Sanner G, Saunders-Pullman R, Vieregge P, Wahlström J, Breakefield XO, Kramer PL, Ozelius LJ, Sealfon SC. Klein C, et al. Among authors: bressman s. Ann Neurol. 2000 Mar;47(3):369-73. Ann Neurol. 2000. PMID: 10716258

4

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.

5

State of the art review: molecular diagnosis of inherited movement disorders. Movement Disorders Society task force on molecular diagnosis.

Gasser T, Bressman S, Dürr A, Higgins J, Klockgether T, Myers RH. Gasser T, et al. Among authors: bressman s. Mov Disord. 2003 Jan;18(1):3-18. doi: 10.1002/mds.10338. Mov Disord. 2003. PMID: 12518296 Review.

6

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.

7

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.

8

Increased frequency of the LRRK2 G2019S mutation in an elderly Ashkenazi Jewish population is not associated with dementia.

Saunders-Pullman R, Lipton RB, Senthil G, Katz M, Costan-Toth C, Derby C, Bressman S, Verghese J, Ozelius LJ. Saunders-Pullman R, et al. Among authors: bressman s. Neurosci Lett. 2006 Jul 10;402(1-2):92-6. doi: 10.1016/j.neulet.2006.03.044. Epub 2006 Apr 24. Neurosci Lett. 2006. PMID: 16632201

9

Obsessive-compulsive disorder is not a clinical manifestation of the DYT1 dystonia gene.

Heiman GA, Ottman R, Saunders-Pullman RJ, Ozelius LJ, Risch NJ, Bressman SB. Heiman GA, et al. Am J Med Genet B Neuropsychiatr Genet. 2007 Apr 5;144B(3):361-4. doi: 10.1002/ajmg.b.30431. Am J Med Genet B Neuropsychiatr Genet. 2007. PMID: 17066475 Free PMC article.

10

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

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