Ocular motility in genetically defined autosomal dominant cerebellar ataxia

American Journal of Ophthalmology

Volumn 133, Issue 5, 2002, Pages 718-721

  Durig, Jacques S ^a   Jen, Joanna C ^b   Demer, Joseph L ^a,c  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c JULES STEIN EYE INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACETAZOLAMIDE;

ADULT; AGED; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BINOCULAR CONVERGENCE; CEREBELLAR ATAXIA; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; DISEASE COURSE; DIVERGENT STRABISMUS; EYE MOVEMENT; FEMALE; GAZE; HUMAN; MALE; MOLECULAR GENETICS; NYSTAGMUS; OPHTHALMOLOGY; PRIORITY JOURNAL; SPINOCEREBELLAR DEGENERATION; TREATMENT OUTCOME; VISUAL ACUITY;

EID: 0036248402     PISSN: 00029394     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0002-9394(02)01328-4     Document Type: Article

References (7)

1. Hereditary ataxia
2. Apisodic ataxia type 1 and 2 (familial periodic ataxia/vertigo)
3. SCA-12: Tremor with cerebellar and cortical atrophy is associated with a CAG repeat expansion
4. Ocular movements in essential blepharospasm
5. Spinocerebellar ataxia type 6 with positional vertigo and acetazolamide responsive episodic ataxia
6. Oculomotor phenotypes in autosomal dominant ataxias