Plasma infusions in an infant with Hurler's syndrome
- 28 February 1973
- journal article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 82 (2) , 273-278
- https://doi.org/10.1016/s0022-3476(73)80166-0
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
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- Effect of Leukocyte Transfusion in a Child with Type II MucopolysaccharidosisProceedings of the National Academy of Sciences, 1971
- Induced Degradation of Glycosaminoglycans in Hurler's and Hunter's Syndromes by Plasma InfusionProceedings of the National Academy of Sciences, 1971
- Metachromatic LeukodystrophyArchives of Neurology, 1969
- Hurler and Hunter Syndromes: Mutual Correction of the Defect in Cultured FibroblastsScience, 1968
- The defect in Hurler's and Hunter's syndromes: faulty degradation of mucopolysaccharide.Proceedings of the National Academy of Sciences, 1968
- Enzymes in Cultivated Human Fibroblasts derived from Patients with Down's Syndrome (Mongolism)Nature, 1967
- Hurler's Syndrome: Demonstration of an Inherited Disorder of Connective Tissue in Cell CultureScience, 1965
- OCCURRENCE OF URINARY ACID MUCOPOLYSACCHARIDES IN THE HURLER SYNDROMEProceedings of the National Academy of Sciences, 1957
- Gargoylism – A mucopolysaccharidosisScandinavian Journal of Clinical and Laboratory Investigation, 1951