Hereditary ferritinopathy

Journal of the Neurological Sciences

Volumn 207, Issue 1-2, 2003, Pages 110-111

  Vidal, Ruben ^a   Delisle, Marie Bernadette ^b   Rascol, Olivier ^b   Ghetti, Bernardino ^a  

^a INDIANA UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b TOULOUSE UNIVERSITY HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CERULOPLASMIN; COPPER; FERRITIN; IRON; PROTEIN ANTIBODY; TAU PROTEIN;

ARM; CENTRAL NERVOUS SYSTEM; CEREBELLAR ATAXIA; CEREBELLUM; CHEMICAL ANALYSIS; COGNITIVE DEFECT; CONFERENCE PAPER; CORPUS STRIATUM; DEGENERATIVE DISEASE; DNA SEQUENCE; DYSARTHRIA; EXTRAPYRAMIDAL SYMPTOM; GENE SEQUENCE; HEREDITARY FERRITINOPATHY; HUMAN; IMMUNOHISTOCHEMISTRY; IRON BLOOD LEVEL; KIDNEY BIOPSY; LIVER BIOPSY; MUSCLE BIOPSY; NERVE BIOPSY; NERVE CELL DEGENERATION; NEUROPATHOLOGY; POLYACRYLAMIDE GEL ELECTROPHORESIS; PRIORITY JOURNAL; PROTEIN BLOOD LEVEL; SKIN BIOPSY; TREMOR;

ANIMALS; FERRITINS; HEREDODEGENERATIVE DISORDERS, NERVOUS SYSTEM; HUMANS;

EID: 12244288334     PISSN: 0022510X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-510X(02)00435-5     Document Type: Conference Paper

References (2)

1. Curtis A.R., Fey C., Morris C.M.et al. Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease. Nat. Genet. 28:2001;350-354.
2. Jellinger K. The role of iron in neurodegeneration: prospects for pharmacotherapy of Parkinson's disease. Drugs Aging. 14:1999;115-140.