Plasma infusions in an infant with Hurler's syndrome
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference18 articles.
1. Gargoylism: A mucopolysaccharidosis;Brante;Scand. J. Clin. Lab. Invest.,1952
2. Occurrence of urinary acid mucopolysaccharide in Hurler's syndrome;Dorfman;Proc. Natl. Acad. Sci.,1957
3. Hurler's syndrome: Demonstration of an inherited disorder of connective tissue in cell culture;Danes;Science,1965
4. The defect in Hurler's and Hunter's syndromes: Faulty degradation of mucopolysaccharide;Fratantoni;Proc. Natl. Acad. Sci.,1968
5. Hurler and Hunter syndromes: Mutual correction of the defect in cultured fibroblasts;Fratantoni;Science,1969
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1. Sanfilippo A syndrome in the fetus;Clinical Genetics;2008-04-23
2. Enzymes as agents for the treatment of disease;Clinica Chimica Acta;1992-03
3. Attempted enzyme replacement using human amnion membane implantations in mucopolysaccharidoses;Journal of Inherited Metabolic Disease;1992-01
4. Mucopolysaccharidoses;Advances in Pediatrics;1986
5. Ocular Histopathology of Systemic Mucopolysaccharidosis, Type II-A (Hunter Syndrome, Severe);Ophthalmology;1985-12
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