Cerebral hemosiderosis related to hereditary ceruloplasmin deficiency: A clinical familial study;Hemosiderose cerebrale liee a un deficit hereditaire en ceruloplasmine. Etude clinique d'un cas familial

Revue Neurologique

Volumn 154, Issue 2, 1998, Pages 158-162

  Servan, J ^a   Elghozi, D ^a   Gaynot, S ^a   Duclos, H ^a  

^a CENTRE HOSPITALIER RENÉ DUBOS   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CERULOPLASMIN; FERRITIN; IRON;

ADULT; ARTICLE; BRAIN DISEASE; CASE REPORT; CHROMOSOME 3; GENE MUTATION; HEMOSIDEROSIS; HUMAN; LIVER BIOPSY; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; PROTEIN DEFICIENCY; BLOOD; BRAIN; DEMENTIA; FEMALE; GENETICS; HALLUCINATION; MIDDLE AGED; MOTOR DYSFUNCTION; NUCLEAR FAMILY; PATHOLOGY; REVIEW;

BRAIN; BRAIN DISEASES; CERULOPLASMIN; CHROMOSOMES, HUMAN, PAIR 3; DEMENTIA; FEMALE; FERRITINS; HALLUCINATIONS; HEMOSIDEROSIS; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; MIDDLE AGED; MOVEMENT DISORDERS; NUCLEAR FAMILY;

EID: 0031916001     PISSN: 00353787     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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