Slowing of voluntary and involuntary saccades: An early sign in spinocerebellar ataxia type 7

Annals of Neurology

Volumn 49, Issue 6, 2001, Pages 801-804

  Oh, Andrew K ^a   Jacobson, Kathleen M ^a   Jen, Joanna C ^a   Baloh, Robert W ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AGED; ARTICLE; BRAIN SCINTISCANNING; CASE REPORT; CLINICAL FEATURE; FEMALE; GENE MUTATION; HUMAN; NUCLEOTIDE REPEAT; OPHTHALMOSCOPY; PATHOLOGICAL ANATOMY; PHYSICAL EXAMINATION; PRIORITY JOURNAL; SACCADIC EYE MOVEMENT; SPINOCEREBELLAR DEGENERATION;

ADULT; AGED; FEMALE; FIXATION, OCULAR; HUMANS; MALE; NERVE TISSUE PROTEINS; PEDIGREE; PONS; PURSUIT, SMOOTH; SACCADES; SPINOCEREBELLAR ATAXIAS; TIME FACTORS; TRINUCLEOTIDE REPEAT EXPANSION;

EID: 0034992392     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.1059     Document Type: Article

References (12)

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3. Age-related changes in visual tracking
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5. Analysis of the dynamic mutation in the SCA7 gene shows marked parental effects on CAG repeat transmission
6. A clinicogenetic analysis of six Indian spinocerebellar ataxia (SCA2) pedigrees: The significance of slow saccades in diagnosis
7. Autosomal dominant cerebellar ataxia type I: Clinical features and MRI in families with SCA1, SCA2 and SCA3
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9. Spinocerebellar ataxia type 7 (SCA7): A neurodegenerative disorder with neuronal intranuclear inclusions
10. Relationship between ataxin-1 nuclear inclusions and Purkinje cell specific proteins in SCA-1 transgenic mice
11. Conserved phosphoprotein interaction motif is functionally interchangeable between ataxin-7 and arrestins