Sucrose-Isomaltose Malabsorption

Author:

Gudman-Høyer E.,Krasilnikoff P. A.,Skovbjerg H.

Publisher

Springer US

Reference213 articles.

1. Alpers, D.H., 1977, Protein turnover in intestinal mucosal villus and crypt brush border membranesBiochem. Biophys. Res. Commun 75: 130

2. Ament, M.E., Perera, D.R., and Esther, L.J., 1973, Sucrase-isomaltase deficiency a frequently misdiagnosed disease.J. Pediatr 83: 721

3. Anderson, C.M., and Burke, V., 1975, Disorders of carbohydrate digestion and absorption, in: Paediatric Gastroenterology ( C.M. Anderson and V. Burke, eds.), pp. 199 – 217, Blackwell Scientific Publications, Oxford

4. Anderson, C.M., Messer, M., Townley, R.R.W., Freeman, M., and Robinson, M.J., 1962, Intestinal isomaltase deficiency in patients with hereditary sucrose and starch intolerance Lancet 2: 556 (letter)

5. Anderson, C.M., Messer, M., Townley, R.R.W., and Freeman, M., 1963, Intestinal sucrase and isomaltase deficiency in two siblings Pediatrics 31: 1003

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