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Glucocerebroside
The Multiple Roles of Sphingomyelin in Parkinson's Disease
GLUCOCEREBROSIDE AMELIORATES the METABOLIC Downloaded from SYNDROME in OB/OB MICE
L-Glucosylceramide: Synthesis, Properties, and Resistance
Clinical Policy: Taliglucerase Alfa (Elelyso) Reference Number: CP.PHAR.157 Effective Date: 02/16 Coding Implications Last Review Date: 02/17 Revision Log
Disorders of Sphingolipid Synthesis, Sphingolipidoses, Niemann-Pick Disease Type C and Neuronal Ceroid Lipofuscinoses
Interactions Between Glucosylceramide and Galactosylceramide I3 Sulfate and Microstructures Formed
Enzyme Defects in the Sphingolipidoses and Their Application to Diagnosis*
Molecular Interactions of Neuronal Ceroid Lipofuscinosis Protein CLN3
Glucocerebrosidase: Functions in and Beyond the Lysosome
Analogs of Ceramide That Inhibit Glucocerebroside Synthetase in Mouse Brain
Deficiency of the Hexosaminidase a Activator Protein in a Case of GM2 Gangliosidosis; Variant AB
Genetic Carrier Screening Technical Bulletin
Demonstration of a Deficiency of Glucocerebroside-Cleaving Enzyme in Gaucher's Disease* ROSCOE 0
Supply-Side and Trickle-Down Therapy
Glucosylsphingosine Accumulation in Mice and Patients with Type 2 Gaucher Disease Begins Early in Gestation
AB Variant of Infantile GM2 Gangliosidosis: Deficiency of A
Neuronal Ceroid Lipofuscinosis
Gaucher Disease
Top View
195 Cerebroside Synthesis and Hydrolysis in A
Sphingolipid Metabolism in Leukemic Leukocytes1
Concentrations of an Activator Protein for Sphingolipid Hydrolysis in Liver and Brain Samples from Patients with Lysosomal Storage Diseases
Selective Effects of Glucocerebroside (Gaucher's Storage Material) on Macrophage Cultures
Glial and Neuronal Localization of Cerebroside-Metabo- Lizing Enzymes
Human Metabolism Lecture Notes
Taliglucerase Alfa (Elelyso) Reference Number: ERX.SPMN.138 Effective Date: 10/16 Coding Implications Last Review Date: 09/16 Revision Log
Enzymological Approaches to the Lipidoses
Lysosomal Storage Diseases Carlos Ferreira George Washington University
Lysosomal Storage Diseases
Enzyme Replacement Therapy in Gaucher's Disease: Preliminary Clinical Trial of a New Enzyme Preparation (Glucocerebrosidase) E
In Contrast to the Well Known Fact That Large Amounts of the So
The Development of Gene Therapy for Niemann-Pick Type C Disease
Case Report Niemann-Pick Disease: Report of Two Cases and Review of Literature
PSAP Gene Prosaposin
Exploiting the Potential of Drosophila Models in Lysosomal Storage Disorders: Pathological Mechanisms and Drug Discovery