Multiple system atrophy with a-/hypo-ceruloplasminemia: Distribution of iron in brains of 2 autopsy cases

Clinical Neurology

Volumn 42, Issue 4, 2002, Pages 293-298

  Kurisaki, Hiroshi ^a   Yomono, Harumi ^a   Murayama, Shigeo ^a   Ebisawa, Akira ^a  

^a NONE

Author keywords

Aceruloplasminemia; Brain iron deposition; Multiple system atrophy

Indexed keywords

ANTIPARKINSON AGENT; CERULOPLASMIN; FERRIC FERROCYANIDE; IRON;

ADULT; AGED; ANAMNESIS; ARTICLE; BRAIN LEVEL; CASE REPORT; CEREBELLUM; CLINICAL FEATURE; DENTATE NUCLEUS; DISEASE COURSE; GAIT DISORDER; HUMAN; HUMAN TISSUE; HYPOCERULOPLASMINEMIA; INCIDENCE; MALE; NEUROPATHOLOGY; PARKINSON DISEASE; PONS ANGLE; PROTEIN BLOOD LEVEL; PUTAMEN; SHY DRAGER SYNDROME; SUBSTANTIA NIGRA;

EID: 0036556426     PISSN: 0009918X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (6)

1. Miyajima H, Nishimura Y, Mizoguti K, et al: Familial apoceruloplasmin deficiency with blepharospasm and retinal degeneration. Neurology 37: 761-767, 1987
2. Kato T, Kawanami T, Daimon M, et al: Hereditary ceruloplasmin deficiency: A cerebro-retino-diabetic disease. Neuropathology 17: 71-75, 1997
3. Miyajima H, Kono S, Takahashi Y, et al: Cerebellar ataxia associated with heteroalledlic ceruloplasmin gene mutation. Neurology 57: 2205-2210, 2001
4. Kohno S, Miyajima H, Takahasi Y, et at: Aceruloplasminemia with a novel mutation associated with parkinsonism. Neurogenetics 2: 237-238, 1999