Atypical Hallervorden-Spatz disease with preserved cognition and obtrusive obsessions and compulsions

Movement Disorders

Volumn 20, Issue 7, 2005, Pages 880-886

  Nicholas, Anthony P ^a   Earnst, Kelly S ^a   Marson, Daniel C ^a  

^a The University of Alabama at Birmingham   (United States)

Author keywords

Dystonia; MRI; Neuropsychology; OCD; Pantothenate kinase 2

Indexed keywords

FLUVOXAMINE MALEATE; PANTOTHENATE KINASE; PAROXETINE; TRIHEXYPHENIDYL;

ADULT; ANTICHOLINERGIC EFFECT; ARTICLE; BODY POSTURE; CASE REPORT; CHOREOATHETOSIS; COGNITION; COMORBIDITY; DYSARTHRIA; DYSTONIA; FEMALE; GENE MUTATION; HALLERVORDEN SPATZ DISEASE; HUMAN; INTELLIGENCE QUOTIENT; LABORATORY TEST; MUSCLE TONE; NERVOUSNESS; NEUROPSYCHOLOGICAL TEST; NUCLEAR MAGNETIC RESONANCE IMAGING; OBSESSIVE COMPULSIVE DISORDER; PHYSICAL EXAMINATION; PRIORITY JOURNAL; SIDE EFFECT; STEREOTYPY; STUTTERING; SURVIVAL; SWEAT GLAND DISEASE; SYMPTOM;

ADULT; BRAIN; COGNITION DISORDERS; FEMALE; HALLERVORDEN-SPATZ SYNDROME; HUMANS; MAGNETIC RESONANCE IMAGING; NEUROPSYCHOLOGICAL TESTS; OBSESSIVE-COMPULSIVE DISORDER;

EID: 24144445104     PISSN: 08853185     EISSN: None     Source Type: Journal    
DOI: 10.1002/mds.20476     Document Type: Article

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