The chemistry and control of hereditary lipid diseases
- 31 December 1974
- journal article
- review article
- Published by Elsevier in Chemistry and Physics of Lipids
- Vol. 13 (4) , 271-282
- https://doi.org/10.1016/0009-3084(74)90003-6
Abstract
No abstract availableThis publication has 23 references indexed in Scilit:
- Enzymatic Defect in Fabry's DiseaseNew England Journal of Medicine, 1967
- The Metabolism of Ceramide TrihexosidesPublished by Elsevier ,1967
- The SphingolipidosesNew England Journal of Medicine, 1966
- Demonstration of a deficiency of glucocerebroside-cleaving enzyme in Gaucher's disease.Journal of Clinical Investigation, 1966
- The Metabolism of SphingomyelinPublished by Elsevier ,1966
- The Metabolism of GlucocerebrosidesJournal of Biological Chemistry, 1965
- Metabolism of glucocerebrosides II. Evidence of an enzymatic deficiency in Gaucher's diseaseBiochemical and Biophysical Research Communications, 1965
- The chemical structure of normal human brain and Tay-Sachs gangliosidesBiochemical and Biophysical Research Communications, 1962
- CEREBROSIDE SYNTHESIS IN GAUCHER'S DISEASE *Journal of Clinical Investigation, 1960
- Über die Natur der Phosphatide und anderer Lipoide des Gehirns und der Leber bei der Niemann-Pickschen Krankheit. [12. Mitteilung über Phosphatide.]Hoppe-Seyler´s Zeitschrift Für Physiologische Chemie, 1935