Different molecular mechanisms leading to white matter hypomyelination in infantile onset lysosomal disorders

Neuropediatrics

Volumn 36, Issue 4, 2005, Pages 265-269

  Di Rocco, M ^a   Rossi, A ^a   Parenti, G ^b   Allegri, A E M ^a   Filocamo, M ^a   Pessagno, A ^a   Tortori Donati, P ^a   Minetti, C ^c   Biancheri, Roberta ^a,c  

^a G GASLINI INSTITUTE   (Italy)

^b UNIVERSITY OF NAPLES FEDERICO II   (Italy)

^c UNIVERSITY OF GENOA   (Italy)

Author keywords

Hypomyelination; Infancy; Lysosomal storage disorders

Indexed keywords

ARTICLE; ASTROCYTE; CASE REPORT; CENTRAL NERVOUS SYSTEM; FEMALE; GLOBOID CELL LEUKODYSTROPHY; GM1 GANGLIOSIDOSIS; HUMAN; HYPOMYELINATING LEUKOENCEPHALOPATHY; INFANT; LYSOSOME STORAGE DISEASE; MALE; METABOLIC DISORDER; MYELINATION; NIEMANN PICK DISEASE; OLIGODENDROGLIA; PRIORITY JOURNAL; WHITE MATTER;

AGE OF ONSET; DEMYELINATING DISEASES; FEMALE; GANGLIOSIDOSIS, GM1; HUMANS; INFANT; LEUKODYSTROPHY, METACHROMATIC; LYSOSOMAL STORAGE DISEASES; MAGNETIC RESONANCE IMAGING; MALE;

EID: 24744451950     PISSN: 0174304X     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2005-865863     Document Type: Article

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