An Inborn Defect of Intestinal Absorption of Certain Monosaccharides-Reference-Cited by-同舟云学术

An Inborn Defect of Intestinal Absorption of Certain Monosaccharides

Published:1965-02-01 Issue:209 Volume:40 Page:1-6
ISSN:0003-9888
Container-title:Archives of Disease in Childhood
language:en
Short-container-title:Archives of Disease in Childhood

Author:

Anderson C. M.,Kerry K. R.,Townley R. R. W.

Publisher

BMJ

Subject

Pediatrics, Perinatology and Child Health

Reference21 articles.

1. Intestinal sucrase and isomaltase deficiency in two siblings;Anderson, C.M.; Messer, M.; Townley, R.R.W.; Freeman, M.;Pediatrics,1963

2. Intestinal isomaltose deficiency in patients with hereditary sucrose and starch intolerance;Auricchio, S.; Dahlqvist, A.; Murset, G.; Prader, A.;Lancet,1962

3. Isolated intestinal lactase deficiency in the adult;Auricchio, S.; Dahlqvist, A.; Murset, G.; Prader, A.; Rubino, A.; Landolt, M.; Semenza, G.; Prader, A.;ibid,1963

4. The colorimetric determination of lactic acid in biological material;Barker, S.B.; Summerson, W.H.;J. biol. Chem,1941

5. The use of the d-xylose excretion test in children;Clark, P.A.;Gut,1962

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