Eye movement abnormalities correlate with genotype in autosomal dominant cerebellar ataxia type I

Annals of Neurology

Volumn 43, Issue 3, 1998, Pages 297-302

  Rivaud Pechoux, Sophie ^a,e   Dürr, Alexandra ^a   Gaymard, Bertrand ^b   Cancel, Géraldine ^a   Ploner, Christoph J ^c   Agid, Yves ^a   Brice, Alexis ^a   Pierrot Deseilligny, Charles ^d  

^a Fed de Neurologie ^*  (Germany)

^b Serv d'Explor Fonct Syst Nerveux   (Germany)

^c CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

^d Service de Neurologie I

^e PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CEREBELLAR ATAXIA; CLINICAL ARTICLE; DYSMETRIA; EYE MOVEMENT CONTROL; FEMALE; HUMAN; HYPERMETROPIA; MACHADO JOSEPH DISEASE; MALE; NYSTAGMUS; ONSET AGE; PRIORITY JOURNAL; RISK FACTOR; SACCADIC EYE MOVEMENT; SMOOTH PURSUIT EYE MOVEMENT; TRINUCLEOTIDE REPEAT;

ADOLESCENT; ADULT; AGED; CEREBELLAR ATAXIA; EYE MOVEMENTS; FEMALE; FIXATION, OCULAR; GENES, DOMINANT; GENOTYPE; HUMANS; MALE; MIDDLE AGED; NYSTAGMUS, PHYSIOLOGIC; PURSUIT, SMOOTH; REPETITIVE SEQUENCES, NUCLEIC ACID; SACCADES;

EID: 2642708379     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.410430306     Document Type: Article

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