Hallerborden Spatz disease

Journal of Association of Physicians of India

Volumn 54, Issue APR., 2006, Pages 320-322

  Raji, V ^a   Dhanasegaran, S E ^a   Subramanian, Usha K ^a   Kumar, Suresh S ^a  

^a MADRAS MEDICAL COLLEGE   (India)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ARTICLE; CASE REPORT; HALLERVORDEN SPATZ DISEASE; HUMAN; MAGNETIC RESONANCE ANGIOGRAPHY; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; PATHOPHYSIOLOGY;

ADOLESCENT; HALLERVORDEN-SPATZ SYNDROME; HUMANS; MAGNETIC RESONANCE ANGIOGRAPHY; MAGNETIC RESONANCE IMAGING; MALE;

EID: 33645679551     PISSN: 00045772     EISSN: 00045772     Source Type: Journal    
DOI: None     Document Type: Article

References (4)

1. Zhou B, Westaway SK, Levinsori B, Johnson MA, Gitschier J, Hayflick SJ. A novel pantothenate kinase gene is defective in Hallervorden - Spatz syndrome. Nat Genet 2001;28:345-9.
2. Swaiman KF. Hallervorden - Spatz syndrome and brain iron metabolism. Arch Neurology 1991;48:1285- 93.
3. Susan J, Hayflick, Shawn K, Westaway, Barbara Levinson, Bing Zhou et al. Genetic, Clinical, and Radiographic Delineation of Hallervorden - Spatz Syndrome. N Engl J Med 2003;348:33-40.
4. Sethi KD, Adams RJ, Loring DW, Gammal T. Hallorvordon -Spatz syndrome: clinical and magnetic resonance imaging correlations. Ann Neuro 1988;24:692-94.