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Current Trends in Sphingolipidoses and Allied Disorders

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Table of Contents

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    Book Overview
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    Chapter 1 Simple Ultra-Microtechniques for Genetic Complementation Analysis and Early Prenatal Diagnosis of Sphingolipidoses
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    Chapter 2 Storage and Excretion of Oligosaccharides and Glycopeptides in the Gangliosidoses
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    Chapter 3 Glycoprotein Catabolism in Brain Tissue in the Lysosomal Enzyme Deficiency Diseases
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    Chapter 4 Component forms of Acid Hydrolases in Subcellular Granules from Human Leucocytes
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    Chapter 5 Fetal Pathology and Ultrastructure of Neuropathic Gaucher’s Disease
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    Chapter 6 Recent Observations on Gaucher’s Disease
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    Chapter 7 Studies on the Pathogenesis of Krabbe’s Leukodystrophy: Cellular Reaction of the Brain to Exogenous Galactosylsphingosine, Monogalactosyl Diglyceride, and Lactosylceramide
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    Chapter 8 Chemical Pathology of Krabbe Disease: The Occurrence of Psychosine and Other Neutral Sphingoglycolipids
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    Chapter 9 Glycolipid Metabolism in the Canine form of Globoid Cell Leukodystrophy
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    Chapter 10 Fucosidosis: Clinical, Pathologic, and Biochemical Studies of Five Patients
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    Chapter 11 Variability of Expressivity of α-Fucosidase Deficiency
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    Chapter 12 Fucosidosis
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    Chapter 13 Alpha-L-Fucosidase in Normal and Deficient Individuals
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    Chapter 14 Studies in Metachromatic Leukodystrophy. XIII. Purification of Sulfatase A from Normal Human Liver
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    Chapter 15 p.Nitrocatechol Sulfate for Arylsulfatase Assay: Detection of Metachromatic Leukodystrophy Variants
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    Chapter 16 Arylsulfatases A and B in Metachromatic Leukodystrophy and Maroteaux-Lamy Syndrome: Studies with 4-Methylumbelliferyl Sulfate
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    Chapter 17 Iduronate Sulfatase Determination for the Diagnosis of the Hunter Syndrome and the Detection of the Carrier State
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    Chapter 18 The Enzymic Defects in Morquio and Maroteaux-Lamy Syndrome
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    Chapter 19 Mannosidosis: Studies of the α-D-Mannosidase Isozymes in Health and Disease
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    Chapter 20 Mannosidosis
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    Chapter 21 Hexosaminidases: Multiple Component Enzymes
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    Chapter 22 Purification and Partial Characterization of α-N-Acetylgalactosaminidase from Porcine Liver
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    Chapter 23 Identification of Tay-Sachs Genotypes by Hexosaminidase Analysis of Urine and Tear Samples
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    Chapter 24 Sphingomyelinases and the Genetic Defects in Niemann-Pick Disease
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    Chapter 25 Adrenoleukodystrophy: A Clinical, Pathological and Biochemical Study
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    Chapter 26 Polyunsaturated Fatty Acid Lipidosis: A New Nosological Entity
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    Chapter 27 The Biochemical Defect in Farber’s Disease
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    Chapter 28 Ultrastructure and Peroxidase of Leucocytes in Five Patients with Juvenile form of Ceroid Lipofuscinoses
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    Chapter 29 Ultrastructure and Biochemical Studies of Rat CNS and Viscera after Subcutaneous Injection of Chlorphentermine
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    Chapter 30 Chemical Models and Chemotherapy in the Sphingolipidoses
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    Chapter 31 Chemical Induction of Lysosomal Storage
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    Chapter 32 Glycolipids in Cultured Fetal Tay-Sachs Disease Cerebellar Cells
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    Chapter 33 The Correction, in vitro, of Lysosomal Enzyme Deficiencies by Means of Immunoglobulin-Coated Liposomes
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    Chapter 34 Enzyme Replacement Therapy for the Sphingolipidoses
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    Chapter 35 High-Performance Liquid Chromatographic Analysis of Glycosphingolipids and Phospholipids
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    Chapter 36 Brain Glycoproteins and Recognition Functions: Recognins and Cancer
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    Chapter 37 Lipids and Slow Viruses: Comparison of Measles and SSPE Virions
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    Chapter 38 Conference Summary
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Title
Current Trends in Sphingolipidoses and Allied Disorders
Published by
Springer US, March 2013
DOI 10.1007/978-1-4684-7735-1
ISBNs
978-1-4684-7737-5, 978-1-4684-7735-1
Editors

Volk, Bruno W., Schneck, Larry

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