How broad is the phenotype of Hallervorden-Spatz disease?

Acta Neurologica Scandinavica

Volumn 103, Issue 3, 2001, Pages 201-203

  Hickman, S J ^a,c   Ward, N S ^a   Surtees, R A H ^b   Stevens, J M ^a   Farmer, S F ^a  

^a NATIONAL HOSPITAL FOR NEUROLOGY AND NEUROSURGERY   (United Kingdom)

^b UNIVERSITY COLLEGE LONDON   (United Kingdom)

^c UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

Dystonia; Hallervorden Spatz syndrome; Iron

Indexed keywords

IRON;

ADULT; ARTICLE; AUTOPSY; CASE REPORT; DEMENTIA; DISEASE COURSE; DYSTONIA; FEMALE; HALLERVORDEN SPATZ DISEASE; HUMAN; MOTOR DEVELOPMENT; NUCLEAR MAGNETIC RESONANCE IMAGING; PHENOTYPE;

ADULT; AGE OF ONSET; COGNITION DISORDERS; DYSTONIA; FEMALE; GLOBUS PALLIDUS; HALLERVORDEN-SPATZ SYNDROME; HUMANS; IRON; MAGNETIC RESONANCE IMAGING; MOTOR SKILLS DISORDERS; PHENOTYPE; SUBSTANTIA NIGRA;

EID: 0035134162     PISSN: 00016314     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1600-0404.2001.103003201.x     Document Type: Article

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