Bressman SB - Search Results

1

Saunders-Pullman R, Ozelius L, Bressman SB. Saunders-Pullman R, et al. Among authors: bressman sb. Adv Neurol. 2002;89:185-91. Adv Neurol. 2002. PMID: 11968443 Review. No abstract available.

2

Essential myoclonus.

Bressman S, Fahn S. Bressman S, et al. Adv Neurol. 1986;43:287-94. Adv Neurol. 1986. PMID: 3080850

3

Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews and their recent descent from a small founder population.

Risch N, de Leon D, Ozelius L, Kramer P, Almasy L, Singer B, Fahn S, Breakefield X, Bressman S. Risch N, et al. Nat Genet. 1995 Feb;9(2):152-9. doi: 10.1038/ng0295-152. Nat Genet. 1995. PMID: 7719342

4

Association of a missense change in the D2 dopamine receptor with myoclonus dystonia.

Klein C, Brin MF, Kramer P, Sena-Esteves M, de Leon D, Doheny D, Bressman S, Fahn S, Breakefield XO, Ozelius LJ. Klein C, et al. Proc Natl Acad Sci U S A. 1999 Apr 27;96(9):5173-6. doi: 10.1073/pnas.96.9.5173. Proc Natl Acad Sci U S A. 1999. PMID: 10220438 Free PMC article.

5

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. Neurology. 1999 Apr 22;52(7):1417-21. doi: 10.1212/wnl.52.7.1417. Neurology. 1999. PMID: 10227628

6

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.

7

Genetic testing for early-onset torsion dystonia (DYT1): introduction of a simple screening method, experiences from testing of a large patient cohort, and ethical aspects.

Klein C, Friedman J, Bressman S, Vieregge P, Brin MF, Pramstaller PP, De Leon D, Hagenah J, Sieberer M, Fleet C, Kiely R, Xin W, Breakefield XO, Ozelius LJ, Sims KB. Klein C, et al. Genet Test. 1999;3(4):323-8. doi: 10.1089/gte.1999.3.323. Genet Test. 1999. PMID: 10627938

8

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. Ann Neurol. 2000 Mar;47(3):369-73. Ann Neurol. 2000. PMID: 10716258

9

The parkin gene is not involved in late-onset Parkinson's disease.

Kann M, Hedrich K, Vieregge P, Jacobs H, Müller B, Kock N, Schwinger E, Klein C, Marder K, Harris J, Meija-Santana H, Bressman S, Ozelius LJ, Lang AE, Pramstaller PP. Kann M, et al. Neurology. 2002 Mar 12;58(5):835; author reply 835. doi: 10.1212/wnl.58.5.835. Neurology. 2002. PMID: 11889262 No abstract available.

10

Epsilon-sarcoglycan mutations found in combination with other dystonia gene mutations.

Klein C, Liu L, Doheny D, Kock N, Müller B, de Carvalho Aguiar P, Leung J, de Leon D, Bressman SB, Silverman J, Smith C, Danisi F, Morrison C, Walker RH, Velickovic M, Schwinger E, Kramer PL, Breakefield XO, Brin MF, Ozelius LJ. Klein C, et al. Among authors: bressman sb. Ann Neurol. 2002 Nov;52(5):675-9. doi: 10.1002/ana.10358. Ann Neurol. 2002. PMID: 12402271

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