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Sucrase-isomaltase deficiency, congenital

Known as: Congenital Sucrose-Isomaltose Malabsorption, deficiency of isomaltase, CSID 
An autosomal recessive genetic disorder caused by mutations in the SI gene, encoding sucrase-isomaltase, intestinal. The condition is characterized… 
National Institutes of Health

Papers overview

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1997
1997
Four experiments were conducted to determine growth performance and changes in intestinal microbial populations of growing pigs… 
1990
1990
1. Sucralfate (basic sucrose aluminium sulphate), a topical intestinal agent, was administered in suspension or granule form to… 
1987
1987
The intestinal brush-border enzyme sucrase-isomaltase splits sucrose into its component monosaccharides, glucose and fructose. A… 
1981
1981
A proteodermatan sulfate was extracted from calf skin with 3 M MgCl2 at 4 degrees C in the presence of protease inhibitors and… 
1980
1980
Past investigation has revealed that the circadian rhythm of intestinal sucrase activity in rats is primarily cued by the time of… 
1980
1980
Proteoglycans extracted from normal and arthritic bovine articular cartilage of various ages were fractionated and purified under… 
1978
1978
The cell envelope fraction of Salmonella typhimurium contains an enzyme system which catalyzes transfer of 3-deoxyoctulosonate… 
1972
1972
In a population study on the western coast of Greenland the incidence of sucrose malabsorption was estimated by means of sucrose… 
1971
1971
1. A study is described of the relationships which exist between disaccharide hydrolysis and glucose transport in the small… 
Highly Cited
1963
Highly Cited
1963
The absence of sucrase and isomaltase activity from the duodenal mucosa of two siblings has been demonstrated in biopsy specimens…