Bressman SB - Search Results

1

Phenomenology and classification of dystonia: a consensus update.

Albanese A, Bhatia K, Bressman SB, Delong MR, Fahn S, Fung VS, Hallett M, Jankovic J, Jinnah HA, Klein C, Lang AE, Mink JW, Teller JK. Albanese A, et al. Among authors: bressman sb. Mov Disord. 2013 Jun 15;28(7):863-73. doi: 10.1002/mds.25475. Epub 2013 May 6. Mov Disord. 2013. PMID: 23649720 Free PMC article. Review.

2

Essential myoclonus.

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

3

Acetylcholinesterase activity in patients with torsion dystonia. Measurement in erythrocyte membranes.

Maltese WA, Bressman S, Fahn S, De Vivo DC. Maltese WA, et al. Arch Neurol. 1985 Feb;42(2):154-5. doi: 10.1001/archneur.1985.04060020068018. Arch Neurol. 1985. PMID: 3977644

4

Dystonia in a patient with deletion of 18q.

Gordon MF, Bressman S, Brin MF, de Leon D, Warburton D, Yeboa K, Fahn S. Gordon MF, et al. Mov Disord. 1995 Jul;10(4):496-9. doi: 10.1002/mds.870100415. Mov Disord. 1995. PMID: 7565832

5

Teaching tape for the motor section of the Toronto Western Spasmodic Torticollis Scale.

Comella CL, Stebbins GT, Goetz CG, Chmura TA, Bressman SB, Lang AE. Comella CL, et al. Among authors: bressman sb. Mov Disord. 1997 Jul;12(4):570-5. doi: 10.1002/mds.870120414. Mov Disord. 1997. PMID: 9251076

6

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.

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

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

10

A heteroplasmic mitochondrial complex I gene mutation in adult-onset dystonia.

Simon DK, Friedman J, Breakefield XO, Jankovic J, Brin MF, Provias J, Bressman SB, Charness ME, Tarsy D, Johns DR, Tarnopolsky MA. Simon DK, et al. Among authors: bressman sb. Neurogenetics. 2003 Aug;4(4):199-205. doi: 10.1007/s10048-003-0150-3. Epub 2003 May 17. Neurogenetics. 2003. PMID: 12756609

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