Inherited lipid storage diseases of the central nervous system. [electronic resource]
Producer: 19800324Description: 1-51 p. digitalISSN:- 0045-9380
- Adolescent
- Adult
- Central Nervous System Diseases -- diagnosis
- Child
- Child, Preschool
- Fabry Disease -- diagnosis
- Female
- Gangliosidoses -- diagnosis
- Gaucher Disease -- diagnosis
- Humans
- Infant
- Infant, Newborn
- Leukodystrophy, Globoid Cell -- diagnosis
- Leukodystrophy, Metachromatic -- diagnosis
- Lipid Metabolism, Inborn Errors -- diagnosis
- Male
- Middle Aged
- Mucolipidoses -- diagnosis
- Niemann-Pick Diseases -- diagnosis
- Sandhoff Disease -- diagnosis
- Sphingolipidoses -- diagnosis
- Sphingolipids -- metabolism
- Tay-Sachs Disease -- diagnosis
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Publication Type: Journal Article; Review
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