Different saccadic abnormalities in PINK1 mutation carriers and in patients with non-genetic Parkinson's disease

Journal of Neurology

Volumn 256, Issue 7, 2009, Pages 1192-1194

  Hertel, Susanne ^a   Sprenger, Andreas ^a   Klein, Christine ^a   Kömpf, Detlef ^a   Helmchen, Christoph ^a   Kimmig, Hubert ^a  

^a UNIVERSITY OF LÜBECK   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

BASAL GANGLION; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; DYSMETRIA; EYE MOVEMENT DISORDER; FRONTAL LOBE; GENE; GENE MUTATION; GENETIC SUSCEPTIBILITY; GENOTYPE; HUMAN; LETTER; PARIETAL LOBE; PARKINSON DISEASE; PINK1 GENE; PREFRONTAL CORTEX; PRIORITY JOURNAL; SACCADIC EYE MOVEMENT; STATISTICAL ANALYSIS; STRIATE CORTEX; TASK PERFORMANCE; UNIFIED PARKINSON DISEASE RATING SCALE;

AGED; BASAL GANGLIA; BASAL GANGLIA DISEASES; DIAGNOSIS, DIFFERENTIAL; DNA MUTATIONAL ANALYSIS; EYE MOVEMENTS; FEMALE; GENETIC MARKERS; GENETIC PREDISPOSITION TO DISEASE; GENETIC SCREENING; GENOTYPE; HETEROZYGOTE; HUMANS; MALE; MIDDLE AGED; NEUROLOGIC EXAMINATION; NEUROPSYCHOLOGICAL TESTS; OCULAR MOTILITY DISORDERS; PARKINSON DISEASE; PROTEIN KINASES; PSYCHOMOTOR PERFORMANCE; SACCADES;

EID: 67650450450     PISSN: 03405354     EISSN: 14321459     Source Type: Journal    
DOI: 10.1007/s00415-009-5092-8     Document Type: Letter

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