Adult-onset leukoencephalopathy with vanishing white matter presenting with dementia

Annals of Neurology

Volumn 50, Issue 5, 2001, Pages 665-668

  Prass, Konstantin ^a   Bruandck, Wolfgang ^a   Schroandder, Nicolas W J ^a   Bender, Andreas ^b   Prass, Maria ^a,c   Wolf, Tilo ^a   Van Der Knaap, Marjo S ^d   Zschenderlein, Rolf ^a  

^a HUMBOLDT UNIVERSITY   (Germany)

^b Hohenzollerndamm   (Germany)

^c Eberswalde   (Germany)

^d VU UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; BRAIN BIOPSY; CASE REPORT; CLINICAL EXAMINATION; DEMENTIA; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; LEUKOENCEPHALOPATHY; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; WHITE MATTER;

ADULT; AGE OF ONSET; BIOPSY; BRAIN; BRAIN DISEASES; DEMENTIA; DIAGNOSIS, DIFFERENTIAL; DISEASE PROGRESSION; GENES, RECESSIVE; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; MYELIN SHEATH;

EID: 0034764190     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.1259     Document Type: Article

References (8)

1. The gene for leukoencephalopathy with vanishing white matter is located on chromosome 3q27
2. Diffuse white matter disease in three children: An encephalopathy with unique features on magnetic resonance imaging and proton magnetic resonance spectroscopy
3. Childhood ataxia with diffuse central nervous system hypomyelination
4. A new leukoencephalopathy with vanishing white matter
5. MR imaging of vanishing white matter
6. Phenotypic variation in leukoencephalopathy with vanishing white matter
7. Increased density of oligodendrocytes in childhood ataxia with diffuse central hypomyelination (CACH) syndrome: Neuropathological and biochemical study of two cases
8. Foamy cells with oligodendroglial phenotype in childhood ataxia with diffuse central nervous system hypomyelination syndrome