Slow saccades and other eye movement disorders in spinocerebellar atrophy type 1

Journal of Neurology

Volumn 244, Issue 2, 1997, Pages 105-111

  Klostermann, Wolfgang ^a   Zühlke, Christine ^a   Heide, Wolfgang ^a   Kömpf, Detlef ^a   Wessel, Karl ^a  

^a UNIVERSITY OF LÜBECK   (Germany)

Author keywords

Autosomal dominant cerebellar ataxia; Electro oculography; Slow saccades; Spinocerebellar atrophy type 1

Indexed keywords

ADULT; ARTICLE; BRAIN STEM INJURY; CASE REPORT; CEREBELLAR ATAXIA; CLINICAL FEATURE; EYE MOVEMENT DISORDER; FAMILY STUDY; FEMALE; GENOTYPE; HUMAN; MALE; OPTIC NERVE ATROPHY; PHENOTYPE; PRIORITY JOURNAL; SACCADIC EYE MOVEMENT; SIBLING; SMOOTH PURSUIT EYE MOVEMENT; SPINOCEREBELLAR DEGENERATION; VISUAL ACUITY; VISUAL IMPAIRMENT;

ADULT; DNA; ELECTROOCULOGRAPHY; FEMALE; FOLLOW-UP STUDIES; GENOTYPE; HUMANS; MALE; OCULAR MOTILITY DISORDERS; PHENOTYPE; REPETITIVE SEQUENCES, NUCLEIC ACID; SACCADES; SPINOCEREBELLAR DEGENERATIONS;

EID: 0031018491     PISSN: 03405354     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004150050058     Document Type: Article

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