Add to ORKGThree cats with feline arylsulfatase-B-deficient mucopolysaccharidosis were studied by light and transmission electron microscopy. Membrane-bound cytoplasmic inclusions were present in hepatocytes, bone marrow granulocytes, vascular smooth muscle cells, and fibroblasts in skin, cornea, and cardiac valves. Central nervous system lesions were restricted to mild ventricular dilatation, perithelial cell vacuolation, and, in one animal, cord compression by vertebral exostoses. The lesions in these cats closely resembled those described in human patients with mucopolysaccharidosis VI (Maroteaux-Lamy syndrome)
We report evidence of a dose responsive effect of enzyme replacement therapy in mucopolysaccharidosi...
Mucolipidosis II (ML II), also called I-cell disease, is a unique lysosomal storage disease caused b...
We report studies that suggest enzyme replacement therapy will result in a significant reduction in ...
Three cats with feline arylsulfatase-B-deficient mucopolysaccharidosis were studied by light and tra...
Five cats with feline α-L-iduronidase-deficient mucopolysaccharidosis were studied. Membrane-bound c...
Two long-haired Siamese cats are reported with clinical manifestations of human mucopolysaccharidosi...
Two long-haired Siamese cats are reported with clinical manifestations of human mucopolysaccharidosi...
Two long-haired Siamese cats are reported with clinical manifestations of human mucopolysaccharidosi...
Abstract. Mucopolysaccharidosis VII was diagnosed in a domestic shorthair cat from California. The c...
Mucolipidosis II (ML II), also called I-cell disease, is a unique lysosomal storage disease caused b...
A 3-year-old Siamese/short-haired European cat was referred for clinical disease characterized by dw...
Abstract. A 7-month-old female cat was seen for abnormal facial features and abnormality of gait. Fa...
Abstract. A male cat 12-1 4 weeks old had walking difficulties and an enlarged abdomen. Facial dysmo...
Mucopolysaccharidosis type VI (MPS VI) is a lysosomal storage disease caused by a deficiency of N-ac...
Mucopolysaccharidosis type VI (MPS VI) is an autosomal recessive disease caused by a deficiency of N...
We report evidence of a dose responsive effect of enzyme replacement therapy in mucopolysaccharidosi...
Mucolipidosis II (ML II), also called I-cell disease, is a unique lysosomal storage disease caused b...
We report studies that suggest enzyme replacement therapy will result in a significant reduction in ...
Three cats with feline arylsulfatase-B-deficient mucopolysaccharidosis were studied by light and tra...
Five cats with feline α-L-iduronidase-deficient mucopolysaccharidosis were studied. Membrane-bound c...
Two long-haired Siamese cats are reported with clinical manifestations of human mucopolysaccharidosi...
Two long-haired Siamese cats are reported with clinical manifestations of human mucopolysaccharidosi...
Two long-haired Siamese cats are reported with clinical manifestations of human mucopolysaccharidosi...
Abstract. Mucopolysaccharidosis VII was diagnosed in a domestic shorthair cat from California. The c...
Mucolipidosis II (ML II), also called I-cell disease, is a unique lysosomal storage disease caused b...
A 3-year-old Siamese/short-haired European cat was referred for clinical disease characterized by dw...
Abstract. A 7-month-old female cat was seen for abnormal facial features and abnormality of gait. Fa...
Abstract. A male cat 12-1 4 weeks old had walking difficulties and an enlarged abdomen. Facial dysmo...
Mucopolysaccharidosis type VI (MPS VI) is a lysosomal storage disease caused by a deficiency of N-ac...
Mucopolysaccharidosis type VI (MPS VI) is an autosomal recessive disease caused by a deficiency of N...
We report evidence of a dose responsive effect of enzyme replacement therapy in mucopolysaccharidosi...
Mucolipidosis II (ML II), also called I-cell disease, is a unique lysosomal storage disease caused b...
We report studies that suggest enzyme replacement therapy will result in a significant reduction in ...