Sphingomyelin of red blood cells in lipidosis and in dementia of unknown origin in children.

Author:

Hooghwinkel G. J.,van Gelderen H. H.,Staal A.

Publisher

BMJ

Subject

Pediatrics, Perinatology, and Child Health

Reference16 articles.

1. Cerebral storage diseases. In Neurohistochemistry;Adams, C.W.M.,1965

2. Mental retardation: metachromatic leucodystrophy. In Medical Aspects of Mental Retardation;Austin, J.H.,1965

3. Brain ganglioside pattern in three forms of amaurotic idiocy and in gargoylism;Borri, P.F.; Hooghwinkel, G.J.M.; Edgar, G.W.F.;J. Neurochem,1966

4. The metabolism of sphingomyelin. II. Evidence of an enzymatic deficiency in Niemann-Pick disease;Brady, R.O.; Kanfer, J.N.; Mock, M.B.; Frederickson, D.S.;Proc. nat. Acad. Sci. (Wash.),1966

5. Metabolism of glucocerebrosides. II. Evidence of an enzymatic deficiency in Gaucher's disease;Shapiro, D.;Biochem Biophys. Res. Commun,1965

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