Movement disorder due to aceruloplasminemia and incorrect diagnosis of hereditary hemochromatosis [3]

Journal of Neurology

Volumn 254, Issue 1, 2007, Pages 113-114

  Fasano, Alfonso ^a   Bentivoglio, Anna Rita ^a   Colosimo, Cesare ^a  

^a CATHOLIC UNIVERSITY   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

CERULOPLASMIN; FERRIC ION; FERRITIN; FERROUS ION; IRON;

BRAIN REGION; CLINICAL FEATURE; DIAGNOSTIC ERROR; FERRITIN BLOOD LEVEL; GENE MUTATION; GENETIC DISORDER; HEMOCHROMATOSIS; HEREDITARY ACERULOPLASMINEMIA; HUMAN; LETTER; LIVER BIOPSY; MOTOR DYSFUNCTION; NUCLEAR MAGNETIC RESONANCE IMAGING; PARKINSON DISEASE; PRIORITY JOURNAL; PROTEIN DEFECT;

CERULOPLASMIN; DIAGNOSIS, DIFFERENTIAL; HEMOCHROMATOSIS; HUMANS; MALE; MIDDLE AGED; MOVEMENT DISORDERS;

EID: 33847170221     PISSN: 03405354     EISSN: 14321459     Source Type: Journal    
DOI: 10.1007/s00415-006-0289-6     Document Type: Letter

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