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… (More)
National Institutes of Health

Papers overview

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2009
2009
BACKGROUND & AIMS Congenital sucrase-isomaltase (SI) deficiency is an autosomal-recessive intestinal disorder characterized by a… (More)
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Review
2000
Review
2000
The disaccharide trehalose is widely distributed in nature and can be found in many organisms, including bacteria, fungi, plants… (More)
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1999
1999
ABSTRACTSucrase-isomaltase deficiency is a rare disorder usually manifested as diarrhea in infancy. The presentation of such a… (More)
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1998
1998
BACKGROUND The purpose of this study was to determine if sacrosidase, a liquid produced from Saccharomyces cerevisiae containing… (More)
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Review
1995
Review
1995
Congenital sucrase-isomaltase deficiency is a disorder that affects a person's ability to digest certain sugars. People with this… (More)
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Highly Cited
1993
Highly Cited
1993
The process of wound repair in monolayers of the intestinal epithelial cell line, Caco-2BBe, was analyzed by a combination of… (More)
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1987
1987
Sucrase-isomaltase deficiency is an inherited disaccharidase deficiency that leads to malabsorption of sucrose, with resulting… (More)
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Highly Cited
1985
Highly Cited
1985
A panel of monoclonal antibodies was produced against purified microvillus membranes of human small intestinal enterocytes. By… (More)
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Highly Cited
1975
Highly Cited
1975
Pulmonary H2 excretion was used to quantitate the small bowel transit time in man. This technique is based on the observation… (More)
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Highly Cited
1968
Highly Cited
1968
1. An enzyme, “chondroitinase-ABC,” has been purified to apparent homogeneity from extracts of Proteus vulgaris, NCTC 4636, which… (More)
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