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

[1]  N. Jain.  Essentials of Veterinary Hematology , 1993 .

[2]  J. Kersey,et al.  Bone marrow transplantation for Hurler syndrome: assessment of metabolic correction. , 1986, Birth defects original article series.

[3]  T. Orii,et al.  Glycosaminoglycan excretion in random samples of urine. , 1985, Clinica chimica acta; international journal of clinical chemistry.

[4]  R. Watts.  Molecular Basis of Lysosomal Storage Disorders , 1985 .

[5]  M. Adinolfi,et al.  Strategies for the Correction of Enzymatic Deficiencies in Patients with Mucopoly‐saccharidoses , 1984, Developmental medicine and child neurology.

[6]  M. Borzyskowski.  Management of Neuropathic Bladder in Childhood , 1984, Developmental medicine and child neurology.

[7]  K. Henry,et al.  BONE MARROW TRANSPLANTATION IN MUCOPOLYSACCHARIDOSES , 1984 .

[8]  P. Gasper,et al.  Correction of feline arylsulphatase B deficiency (mucopolysaccharidosis VI) by bone marrow transplantation , 1984, Nature.

[9]  P. Menon,et al.  Mucopolysaccharidosis VI (Maroteaux-Lamy syndrome). , 1983, Indian pediatrics.

[10]  H. Nader,et al.  Clinical and biochemical changes in a child with type I mucopolysaccharidosis during long-term transfusion of leukocytes. , 1983, Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas.

[11]  J. Hopwood,et al.  High-resolution electrophoresis of urinary glycosaminoglycans: an improved screening test for the mucopolysaccharidoses. , 1982, Analytical biochemistry.

[12]  R. Desnick,et al.  Animal model of human disease: Mucopolysaccharidosis VI Maroteaux-Lamy syndrome, Arylsulfatase B-deficient mucopolysaccharidosis in the Siamese cat. , 1981, The American journal of pathology.

[13]  T. Anastassiades,et al.  Quantitation and interaction of glycosaminoglycans with Alcian blue in dimethyl sulfoxide solutions. , 1979, Analytical biochemistry.

[14]  M. Haskins,et al.  Mucopolysaccharidosis in a cat with arylsulfatase B deficiency: a model of Maroteaux-Lamy syndrome , 1977, Science.

[15]  G. Constantopoulos,et al.  Effects of fresh plasma or whole blood transfusions on patients with various types of mucopolysaccharidosis. , 1972, Pediatrics.

[16]  B. Nichols,et al.  Induced degradation of glycosaminoglycans in Hurler's and Hunter's syndromes by plasma infusion. , 1971, Proceedings of the National Academy of Sciences of the United States of America.

[17]  M. Mott,et al.  Screening for mucopolysaccharidoses. , 1970, Clinica chimica acta; international journal of clinical chemistry.

[18]  K. S. Dodgson,et al.  The assay of arylsulphatases A and B in human urine. , 1959, Clinica chimica acta; international journal of clinical chemistry.

[19]  W. S. Beck,et al.  Studies on the fibrinogen, dextran and phytohemagglutinin methods of isolating leukocytes. , 1956, Blood.