Clinical report of three patients with hereditary hemochromatosis and movement disorders

Movement Disorders

Volumn 15, Issue 6, 2000, Pages 1204-1209

  Demarquay, G ^a,b   Setiey, A ^b   Morel, Y ^c   Trepo, C ^d   Chazot, G ^a   Broussolle, E ^a  

^a HÔPITAL NEUROLOGIQUE   (France)

^b Department of Neurology   (France)

^c HÔPITAL DEBROUSSE   (France)

^d HÔTEL DIEU   (France)

Author keywords

Cerebellar syndrome; Chronic acquired hepatocerebral degeneration; Dystonia; Hereditary hemochromatosis; Iron; Movement disorders; Parkinsonism; Tremor

Indexed keywords

AMANTADINE; BUSPIRONE; CLONAZEPAM; FEBARBAMATE; FERRITIN; IRON; LEVODOPA; PRIMIDONE; ROPINIROLE; TRIHEXYPHENIDYL; VALPROIC ACID;

ADULT; AGED; ANAMNESIS; ARTICLE; BRAIN ATROPHY; CASE REPORT; CEREBELLUM ATROPHY; DEMENTIA; FEMALE; FERRITIN BLOOD LEVEL; GENE MUTATION; GENETIC DISORDER; HEMOCHROMATOSIS; HEPATIC ENCEPHALOPATHY; HUMAN; IRON BLOOD LEVEL; LIVER BIOPSY; LIVER FAILURE; MALE; MOTOR DYSFUNCTION; MYOCLONUS; NUCLEAR MAGNETIC RESONANCE IMAGING; PARKINSONISM; PHLEBOTOMY; PRIORITY JOURNAL; TREMOR; WHITE MATTER;

ADULT; AGED; FEMALE; HEMOCHROMATOSIS; HEPATOLENTICULAR DEGENERATION; HUMANS; IRON; MALE; MOVEMENT DISORDERS;

EID: 0033709765     PISSN: 08853185     EISSN: None     Source Type: Journal    
DOI: 10.1002/1531-8257(200011)15:6<1204::AID-MDS1021>3.0.CO;2-T     Document Type: Article

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