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Home > Current Trends in Sphingolipidoses and Allied Disorders > Studies in Metachromatic Leukodystrophy. XIII. Purification of Sulfatase A from Normal Human Liver
Current Trends in Sphingolipidoses and Allied Disorders |
Bruno Volk
Springer US
Current Trends in Sphingolipidoses and Allied Disorders
Studies in Metachromatic Leukodystrophy. XIII. Purification of Sulfatase A from Normal Human Liver
Authors

Janet Collins; Warren Yamada; William Worth; James Austin

ARI Id

1664339762160_1280773

Access

Not Available Free

Pages

225-232

DOI

10.1007/978-1-4684-7735-1_14

Chapter URL

https://rd.springer.com/chapter/10.1007/978-1-4684-7735-1_14

Table of Contents of Book
Showing 1 to 20 of 40 entries
Chapters/HeadingsAuthor(s)PagesInfo
Front Matter
i-xi
Simple Ultra-Microtechniques for Genetic Complementation Analysis and Early Prenatal Diagnosis of Sphingolipidoses
P. Hösli
1-13
Storage and Excretion of Oligosaccharides and Glycopeptides in the Gangliosidoses
Leonhard S. Wolfe; N. M. K. Ng Ying Kin
15-29
Glycoprotein Catabolism in Brain Tissue in the Lysosomal Enzyme Deficiency Diseases
Eric G. Brunngraber; Leonard G. Davis; Javaid I. Javaid; Bruno Berra
31-48
Component forms of Acid Hydrolases in Subcellular Granules from Human Leucocytes
R. B. Ellis; A. D. Patrick
49-62
Fetal Pathology and Ultrastructure of Neuropathic Gaucher’s Disease
Shigehiko Kamoshita; Mariko Odawara; Mariko Yoshida; Misao Owada; Teruo Kitagawa
63-75
Recent Observations on Gaucher’s Disease
J. N. Kanfer; S. S. Raghaven; R. A. Mumford; J. Sullivan; C. Spielvogel; G. Legler et al.
77-98
Studies on the Pathogenesis of Krabbe’s Leukodystrophy: Cellular Reaction of the Brain to Exogenous Galactosylsphingosine, Monogalactosyl Diglyceride, and Lactosylceramide
Kinuko Suzuki; Harumi Tanaka; Kunihiko Suzuki
99-114
Chemical Pathology of Krabbe Disease: The Occurrence of Psychosine and Other Neutral Sphingoglycolipids
Marie-Thérèse Vanier; Lars Svennerholm
115-126
Glycolipid Metabolism in the Canine form of Globoid Cell Leukodystrophy
Elvira Costantino-Ceccarini; Thomas F. Fletcher; Kunihiko Suzuki
127-145
Fucosidosis: Clinical, Pathologic, and Biochemical Studies of Five Patients
Benjamin H. Landing; George N. Donnell; Omar S. Alfi; Harry B. Neustein; Fred A. Lee; Won G. Ng et al.
147-165
Variability of Expressivity of α-Fucosidase Deficiency
Vimalkumar Patel; Wolfgang Zeman
167-186
Fucosidosis
Glyn Dawson; Grace Chen Tsay
187-203
Alpha-L-Fucosidase in Normal and Deficient Individuals
Kurt Hirschhorn; Nicholas G. Beratis; Bryan M. Turner
205-223
Studies in Metachromatic Leukodystrophy. XIII. Purification of Sulfatase A from Normal Human Liver
Janet Collins; Warren Yamada; William Worth; James Austin
225-232
p. Nitrocatechol Sulfate for Arylsulfatase Assay: Detection of Metachromatic Leukodystrophy Variants
Gisèle Dubois; Jean-Claude Turpin; Nicole Baumann
233-237
Arylsulfatases A and B in Metachromatic Leukodystrophy and Maroteaux-Lamy Syndrome: Studies with 4-Methylumbelliferyl Sulfate
Edwin H. Kolodny; Richard A. Mumford
239-251
Iduronate Sulfatase Determination for the Diagnosis of the Hunter Syndrome and the Detection of the Carrier State
Elizabeth F. Neufeld; Ingeborg Liebaers; Timple W. Lim
253-260
The Enzymic Defects in Morquio and Maroteaux-Lamy Syndrome
Albert Dorfman; Bradley Arbogast; Reuben Matalon
261-276
Mannosidosis: Studies of the α-D-Mannosidase Isozymes in Health and Disease
R. J. Desnick; L. L. Walling; P. M. Anderson; M. K. Raman; H. L. Sharp; J. U. Ikonne
277-299
Chapters/HeadingsAuthor(s)PagesInfo
Showing 1 to 20 of 40 entries
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