Excretion of mannose-rich complex carbohydrates by a patient with α-mannosidase deficiency (mannosidosis)
- 30 June 1974
- journal article
- research article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 84 (6), 865-868
- https://doi.org/10.1016/s0022-3476(74)80768-7
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Mannosidosis in angus cattle: Partial characterization of two mannose containing oligosaccharidesFEBS Letters, 1973
- Urinary mannose in mannosidosisThe Journal of Pediatrics, 1973
- Deficiency of α-mannosidase in Angus cattle. An inherited lysosomal storage diseaseBiochemical Journal, 1972
- Lactosylceramidosis: Lactosylceramide galactosyl hydrolase deficiency and accumulation of lactosylceramide in cultured skin fibroblastsThe Journal of Pediatrics, 1971
- Quantitative levels of the constituents of acid mucopolysaccharides and other carbohydrate polymers in dialyzed normal human urineClinica Chimica Acta; International Journal of Clinical Chemistry, 1971
- The simultaneous estimation of 6-deoxy-l-galactose (l-fucose), d-mannose, d-galactose, 2-acetamido-2-deoxy-d-glucose (N-acetyl-d-glucosamine) and N-acetylneuraminic acid (sialic acid) in glycopeptides and glycoproteinsBiochimica et Biophysica Acta (BBA) - General Subjects, 1967
- A GENERALISED STORAGE DISORDER RESEMBLING HURLER'S SYNDROMEThe Lancet, 1967