A form of inherited cerebellar ataxia with saccadic intrusions, increased saccadic speed, sensory neuropathy, and myoclonus

Annals of the New York Academy of Sciences

Volumn 956, Issue , 2002, Pages 441-444

  Swartz, Barbara E ^a   Burmeister, Margit ^b   Somers, Jeffrey T ^c   Rottach, Klaus G ^d   Bespalova, Irina N ^b   Leigh, R John ^a  

^a CASE WESTERN RESERVE UNIVERSITY   (United States)

^b UNIVERSITY OF MICHIGAN   (United States)

^c NASA JOHNSON SPACE CENTER   (United States)

^d NONE   (Germany)

Author keywords

Ataxia; Cerebellum; Saccades

Indexed keywords

ADULT; CLINICAL ARTICLE; CLINICAL FEATURE; CONFERENCE PAPER; EYE FIXATION; EYE MOVEMENT DISORDER; EYE POSITION; FAMILY STUDY; FEMALE; HEREDITARY ATAXIA; HUMAN; MALE; MYOCLONUS; ONSET AGE; OSCILLATION; SACCADIC EYE MOVEMENT; SENSORY NEUROPATHY; VELOCITY;

ATAXIA;

EID: 0036237387     PISSN: 00778923     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1749-6632.2002.tb02850.x     Document Type: Article

References (6)

1. Hereditary ataxias
2. Dynamic properties of horizontal and vertical eye movements in parkinsonian syndromes
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4. Fixation instability and oculomotor abnormalities in Friedreich's ataxia
5. Role of the caudal fastigial nucleus in saccade generation. II. Effects of muscimol inactivation