Perry syndrome: A disorder to consider in the differential diagnosis of Parkinsonism

Journal of the Neurological Sciences

Volumn 330, Issue 1-2, 2013, Pages 117-118

  Aji, B M ^a   Medley, G ^a   O'Driscoll, K ^a   Larner, A J ^a   Alusi, S H ^a  

^a WALTON CENTRE FOR NEUROLOGY AND NEUROSURGERY   (United Kingdom)

Author keywords

DCTN1 mutation; Diagnosis; Parkinsonism; Perry syndrome; Phenotype

Indexed keywords

CITALOPRAM; LEVODOPA; PROGRANULIN; PROTEIN; SERTRALINE; VENLAFAXINE;

ADULT; ANXIETY; ARTICLE; CASE REPORT; CEREBROSPINAL FLUID; CHROMOSOME 17; DEPRESSION; DIFFERENTIAL DIAGNOSIS; DISEASE COURSE; DRUG TREATMENT FAILURE; DYSPNEA; ELECTROENCEPHALOGRAM; GENE MUTATION; GENERAL CONDITION DETERIORATION; HUMAN; INVOLUNTARY MOVEMENT; MALE; MEMORY; NIGHT SLEEP; PARKINSONISM; PERRY SYNDROME; PHENOTYPE; PRIORITY JOURNAL; PROGRESSIVE SUPRANUCLEAR PALSY; PSYCHOSOCIAL WITHDRAWAL; REM SLEEP; RESPIRATORY FAILURE; SACCADIC EYE MOVEMENT; TACHYPNEA; VISUAL MEMORY; WEIGHT REDUCTION;

ANXIETY; DEPRESSION; DIAGNOSIS, DIFFERENTIAL; GENETIC TESTING; HUMANS; HYPOVENTILATION; MALE; MICROTUBULE-ASSOCIATED PROTEINS; MIDDLE AGED; MOOD DISORDERS; MUTATION; PARKINSON DISEASE; PARKINSONIAN DISORDERS; RESPIRATORY INSUFFICIENCY; SLEEP DISORDERS; SYNDROME;

EID: 84878572778     PISSN: 0022510X     EISSN: 18785883     Source Type: Journal    
DOI: 10.1016/j.jns.2013.04.008     Document Type: Article

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