Neurodegenerative course in ceramidase deficiency (Farber disease) correlates with the residual lysosomal ceramide turnover in cultured living patient cells

Author:

Levade Thierry,Moser Hugo W.,Fensom Anthony H.,Harzer Klaus,Moser Ann B.,Salvayre Robert

Publisher

Elsevier BV

Subject

Clinical Neurology,Neurology

Reference50 articles.

1. Properties of acid ceramidase from human spleen;Al;Biochim. Biophys. Acta,1989

2. Phenotypic variability in siblings with Farber disease;Antonarakis;J. Pediatr.,1984

3. Sphingomyelins in bilayers and biological membranes;Barenholz;Biochim. Biophys. Acta,1980

4. Role of lysosomal acid ceramidase in the metabolism of ceramide in human skin fibroblasts;Chen;Arch. Biochem. Biophys.,1981

5. Neurologic progressive form (type 5) of Farber's lipogranulomatosis (ceramidase deficiency) in monozygotic twins;Colamaria,1992

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