Urine glycosaminoglycan concentrations in mucopolysaccharidosis VI-affected cats following bone marrow transplantation or leukocyte infusion

Author:

Dial Sharon M,Byrne Thomas,Haskins Mark,Gasper Peter W,Rose Barbara,Wenger David A,Thrall Mary Anna

Publisher

Elsevier BV

Subject

Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine

Reference17 articles.

1. Neufeld EF, Muenzer J. The mucopolysaccharidoses. In: Scriver CR, Beaudet AL, Sly WS, Valle D, editors. The Metabolic and Molecular Basis of Inherited Disease, 7th ed, New York: McGraw–Hill, 1989:2465–94.

2. Mucopolysaccharidosis in a cat with arylsulfatase B deficiency: A model of Maroteaux–Lamy Syndrome.;Jezyk;Science,1977

3. Animal models of human disease. Mucopolysaccharidosis VI (Maroteaux–Lamy Syndrome).;Haskins;Am J Pathol,1981

4. Clinical and biochemical changes in a child with Type I mucopolysaccharidosis during long term transfusion of leukocytes.;Toma;Brazilian J Med Biol Res,1983

5. Effects of fresh plasma or whole blood transfusions on patients with various types of mucopolysaccharidosis.;Dekaban;Pediatrics,1972

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1. Mucopolysaccharidosis Type VI, an Updated Overview of the Disease;International Journal of Molecular Sciences;2021-12-15

2. New treatment method for mucopolysaccharidosis type VI by liver transplantation;Pediatrics International;2018-12-13

3. Adapted colorimetric method for measurement of feline urinary glycosaminoglycans;Comparative Clinical Pathology;2012-09-30

4. Gene Therapy for Lysosomal Storage Diseases (LSDs) in Large Animal Models;ILAR Journal;2009-01-01

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