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Titlebook: Sphingolipids, Sphingolipidoses and Allied Disorders; Proceedings of the S Bruno W. Volk,Stanley M. Aronson Conference proceedings 1972 The

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Human Brain Lipid Composition Changes with Age and Alterations in Some Pathological States: A New Mompared to that of normal brain by plotting values as percentage of the fresh weight against age and noting whether or not values are within the normal range. Abnormal proportions of lipid classes are disclosed by plotting values for each lipid class against the value for total phospholipid. This me
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A Fast Moving Protein in Tay-Sachs Disease, that it might represent a disease-specific substance. Later on, Zeman et al. (1970). showed that this protein was not present in the brains of all patients with Tay-Sachs disease although the resolution of their techniques was probably not sufficient to detect concentrations of less than 10% of the
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The Degradation of Acid Mucopolysaccharides and the Mucopolysaccharidoses,eases characterized by the accumulation in tissues and excretion in urine of acid mucopolysaccharides. These studies have been reviewed by McKusick (28) and Dorfman and Matalon (11,12). The term mucopolysaccharidoses was originally suggested by Brante (1) who discovered that the storage material pre
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Interaction of Enzymes with Lipid Substrates,racterization of the enzymes which synthesize and degrade the sphingolipids; the identification of separate phospholipases A. and A.; the identification of a new pathway for phosphoglyceride biosynthesis via acyl dihydroxyacetone phosphate and further recognition of the enzymes which synthesize and
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