Foamy cells with oligodendroglial phenotype in childhood ataxia with diffuse central nervous system hypomyelination syndrome

Acta Neuropathologica

Volumn 100, Issue 6, 2000, Pages 635-646

  Wong, K ^a   Armstrong, Regina C ^b   Gyure, Kymberly A ^a   Morrison, Alan L ^a   Rodriguez, Diana ^c   Matalon, Reuben ^d   Johnson, Anne B ^e   Wollmann, Robert ^f   Gilbert, Enid ^g   Le, Tuan Q ^b   Bradley, Courtney A ^b   Crutchfield, Kevin ^h   Schiffmann, Raphael ^h  

^a ARMED FORCES INSTITUTE OF PATHOLOGY   (United States)

^b UNIFORMED SERVICES UNIVERSITY OF THE HEALTH SCIENCES   (United States)

^c HÔPITAL SAINT VINCENT DE PAUL   (France)

^d UNIVERSITY OF TEXAS MEDICAL BRANCH   (United States)

^e ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

^f UNIVERSITY OF CHICAGO MEDICAL CENTER   (United States)

^g TAMPA GENERAL HOSPITAL   (United States)

^h NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE   (United States)

Author keywords

Childhood ataxia with diffuse central nervous system hypomyelination (CACH syndrome); Leukodystrophy; Myelin; Oligodendroglia

Indexed keywords

MESSENGER RNA; PROTEOLIPID PROTEIN; TOLONIUM CHLORIDE;

ANTIBODY LABELING; ARTICLE; ATAXIA; BRAIN TISSUE; CELL STRUCTURE; CENTRAL NERVOUS SYSTEM DISEASE; CHILD; CHILDHOOD DISEASE; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; ELECTRON MICROSCOPY; FEMALE; FOAM CELL; HUMAN; HUMAN CELL; HUMAN TISSUE; IN SITU HYBRIDIZATION; LEUKODYSTROPHY; LYSOSOME; MACROPHAGE; MALE; MYELIN DEFICIENCY; MYELINATION; NEUROPATHOLOGY; OLIGODENDROGLIA; PATHOGENESIS; PHENOTYPE; PRIORITY JOURNAL; RNA TRANSCRIPTION; STAINING; STRUCTURE ANALYSIS; WHITE MATTER;

ATAXIA; BIOLOGICAL MARKERS; BIOPSY; BRAIN; CHILD; CHILD, PRESCHOOL; FEMALE; FOAM CELLS; HEREDITARY CENTRAL NERVOUS SYSTEM DEMYELINATING DISEASES; HUMANS; INFANT; MALE; OLIGODENDROGLIA; PHENOTYPE; RNA, MESSENGER;

EID: 0033770347     PISSN: 00016322     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004010000234     Document Type: Article

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