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117977
Inherited lipid storage diseases of the central nervous system.

Curr Probl Pediatr, 1979/9;9(11):1-51.

Percy AK, Shapiro LJ, Kaback MM

PMID: 117977

MeSH terms
Adolescent; Adult; Central Nervous System Diseases; Child; Child, Preschool; Fabry Disease; Female; Gangliosidoses; Gaucher Disease; Humans; Infant; Infant, Newborn; Leukodystrophy, Globoid Cell; Leukodystrophy, Metachromatic; Lipid Metabolism, Inborn Errors; Male; Middle Aged; Mucolipidoses; Niemann-Pick Diseases; Sandhoff Disease; Sphingolipidoses; Sphingolipids; Tay-Sachs Disease
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