SCOPUS 정보 검색 플랫폼

Journal of Neurology

Volumn 250, Issue 7, 2003, Pages 793-796

An unusual family with multiple movement disorders

(6) Edwards, Mark d Russo, Noemi d Summers, Beatrice a Morton, Jenny b Peake, Deirdre c Bhatia, Kailash d

a STAFFORDSHIRE GENERAL HOSPITAL (United Kingdom)

b Clinical Genetics Unit (United Kingdom)

c BIRMINGHAM CHILDREN S HOSPITAL (United Kingdom)

d UNIVERSITY COLLEGE LONDON (United Kingdom)

Author keywords

Generalized dystonia; Huntington's disease

Indexed keywords

ADULT; ARTICLE; CHOREA; CLINICAL ARTICLE; DYSKINESIA; DYSTONIA; FEMALE; GENE DELETION; GENE LOCATION; HUMAN; HUNTINGTON CHOREA; MALE; MOTOR DYSFUNCTION; PRIORITY JOURNAL; PROGRESSIVE SUPRANUCLEAR PALSY;

ADOLESCENT; ADULT; FEMALE; HUMANS; MALE; MIDDLE AGED; MOVEMENT DISORDERS; PEDIGREE;

EID: 0042347776 PISSN: 03405354 EISSN: None Source Type: Journal
DOI: 10.1007/s00415-003-1078-0 Document Type: Article

Times cited : (3)

References (5)

1
- 0035297119
- Intrafamilial heterogenicity of facial hyperkinesias: Chance association of tics, cranial dystonia and Huntington's disease
- Muller J, Wenning GK, Wissel J, Poewe W (2001) Intrafamilial heterogenicity of facial hyperkinesias: chance association of tics, cranial dystonia and Huntington's disease. Mov Dis 16:370-371
- (2001) Mov Dis , vol.16 , pp. 370-371
- Muller, J.¹ Wenning, G.K.² Wissel, J.³ Poewe, W.⁴

2
- 0027988344
- Dystonia in Ashkenazi Jews: Clinical characterisation of a founder mutation
- Bressman SB, de Leon D, Kramer PL, et al. (1994) Dystonia in Ashkenazi Jews: clinical characterisation of a founder mutation. Ann Neurol 36:771-777
- (1994) Ann Neurol , vol.36 , pp. 771-777
- Bressman, S.B.¹ De Leon, D.² Kramer, P.L.³

3
- 16944366666
- The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein
- Ozelius LJ, Hewett JW, Page CE, Bressman SB, Kramer PL, Shalish C, de Leon D, et al. (1997) The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein. Nat Genet 17(1):40-48
- (1997) Nat Genet , vol.17 , Issue.1 , pp. 40-48
- Ozelius, L.J.¹ Hewett, J.W.² Page, C.E.³ Bressman, S.B.⁴ Kramer, P.L.⁵ Shalish, C.⁶ De Leon, D.⁷

4
- 0033828549
- Dystoniapredominant adult-onset Huntington disease: Association between motor phenotype and age of onset in adults
- Louis ED, Anderson KE, Moskowitz C, Thorne DZ, Marder K (2000) Dystoniapredominant adult-onset Huntington disease: association between motor phenotype and age of onset in adults. Arch Neurol 57(9):1326-1330
- (2000) Arch Neurol , vol.57 , Issue.9 , pp. 1326-1330
- Louis, E.D.¹ Anderson, K.E.² Moskowitz, C.³ Thorne, D.Z.⁴ Marder, K.⁵

5
- 0036370657
- Secondary causes of paroxysmal dyskinesia
- Blakeley J, Jankovic J (2002) Secondary causes of paroxysmal dyskinesia. Adv Neurol 89:401-420
- (2002) Adv Neurol , vol.89 , pp. 401-420
- Blakeley, J.¹ Jankovic, J.²

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.