Incorporation and degradation of GM1 ganglioside and asialoGm1 ganglioside in cultured fibroblasts from normal individuals and patients with β-galactosidase deficiency

This publication has 35 references indexed in Scilit:

• Morquio B syndrome: A primary defect in β‐galactosidase
  American Journal of Medical Genetics, 1983
• β‐Galactosidase–neuraminidase deficiency (galactosialidosis): Clinical, pathological, and enzymatic studies in a postmortem case
  Annals of Neurology, 1983
• Chronic G_M1 gangliosidosis presenting as dystonia: I. Clinical and pathological features
  Annals of Neurology, 1981
• Enzymatic phosphorylation of lysosomal enzymes in the presence of UDP-N-acetylglucosamine. Absence of the activity in l-cell fibroblasts
  Biochemical and Biophysical Research Communications, 1981
• Adult Gmi gangliosidosis: Clinical and biochemical studies on two patients and comparison to other patients called variant or adult Gm1 gangliosidosis
  Clinical Genetics, 1980
• Macular cherry-red spots and myoclonus with dementia: Coexistent neuraminidase and β-galactosidase deficiencies
  Biochemical and Biophysical Research Communications, 1978
• Macular Cherry-Red Spots and β-Galactosidase Deficiency in an Adult
  Archives of Neurology, 1977
• ?-Galactosidase deficiency in juvenile and adult patients
  Human Genetics, 1977
• Morquio‐like syndrome with beta galactosidase deficiency and normal hexosamine sulfatase activity: Mucopolysaccharidosis IVB
  American Journal of Medical Genetics, 1977
• Spondyloepiphyseal dysplasia, corneal clouding, normal intelligence and acid β‐galactosidase deficiency
  Clinical Genetics, 1976