Current Trends in Sphingolipidoses and Allied Disorders

Simple Ultra-Microtechniques for Genetic Complementation Analysis and Early Prenatal Diagnosis of Sphingolipidoses.- Storage and Excretion of Oligosaccharides and Glycopeptides in the Gangliosidoses.- Glycoprotein Catabolism in Brain Tissue in the Lysosomal Enzyme Deficiency Diseases.- Bruno Berra Component Forms of Acid Hydrolases in Subcellular Granules from Human Leucocytes.- Fetal Pathology and Ultrastructure of Neuropathic Gaucher’s Disease.- Recent Observations on Gaucher’s Disease.- Studies on the Pathogenesis of Krabbe’s Leukodystrophy: Cellular Reaction of the Brain to Exogenous Galactosylsphingosine, Monogalactosyl Diglyceride and Lactosylceramide.- Chemical Pathology of Krabbe Disease: The Occurrence of Psychosine and Other Neutral Sphingoglycolipids.- Glycolipid Metabolism in the Canine Form of Globoid Cell Leukodystrophy.- Fucosidosis: Clinical, Pathologic and Biochemical Studies of Five Patients.- Variability of Expressivity of ?-Fucosidase Deficiency.- Fucosidosis.- Alpha-L-Fucosidase in Normal and Deficient Individuals.- Studies in Metachromatic Leukodystrophy. XIII. Purification of Sulfatase A from Normal Human Liver.- p.Nitrocatechol Sulfate for Arylsulfatase Assay: Detection of Metachromatic Leukodystrophy Variants.- Arylsulfatases A and B in Metachromatic Leukodystrophy and Maroteaux-Lamy Syndrome: Studies with 4-Methylumbelliferyl Sulfate.- Iduronate Sulfatase Determination for the Diagnosis of the Hunter Syndrome and the Detection of the Carrier State.- The Enzymic Defects in Morquio and Maroteaux-Lamy Syndrome.- Mannosidosis: Studies of the ?-D-Mannosidase Isozymes in Health and Disease.- Mannosidosis: Storage Material, ?-Mannosidase Specificity and Diagnostic Methods.- Hexosaminidases: Multiple Component Enzymes.- Purification andPartial Characterization of ?-N-Acetylgalactosaminidase from Porcine Liver.- Identification of Tay-Sachs Genotypes by Hexosaminidase Analysis of Urine and Tear Samples.- Sphingomyelinases and the Genetic Defects in Niemann-Pick Disease.- Adrenoleukodystrophy: A Clinical Pathological and Biochemical Study.- Polyunsaturated Fatty Acid Lipidosis: A New Nosological Entity.- The Biochemical Defect in Farber’s Disease.- Ultrastructure and Peroxidase of Leucocytes in Five Patients with Juvenile Form of Ceroid Lipofuscinoses.- Ultrastructure and Biochemical Studies of Rat CNS and Viscera After Subcutaneous Injection of Chlorphentermine.- Chemical Models and Chemotherapy in the Sphingolipidoses.- Chemical Induction of Lysosomal Storage.- Glycolipids in Cultured Fetal Tay-Sachs Disease Cerebellar Cells.- The Correction, In Vitro, of Lysosomal Enzyme Deficiencies by Means of Immunoglobulin-Coated Liposomes.- Enzyme Replacement Therapy for the Sphingolipidoses.- High-Performance Liquid Chromatographic Analysis of Glycosphingolipids and Phospholipids.- Brain Glycoproteins and Recognition Functions: Recognins and Cancer.- Lipids and Slow Viruses: Comparison of Measles and SSPE Virions.- Conference Summary.- Contributors and Participants.