Clinical heterogeneity in congenital sucrase-isomaltase deficiency
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference15 articles.
1. Glucose polymer as a cause of protracted diarrhea in infants with unsuspected congenital sucrase-isomaltase deficiency;Newton;J Pediatr,1996
2. Properties of human intestinal glucoamylase;Kelly;Biochem Biophys Acta,1973
3. Congenital sucrase-isomaltase deficiency;Treem;J Pediatr Gastroenterol Nutr,1995
4. Sucrase-isomaltase (palatinasc) deficiency diagnosed during adulthood;Ringrose;Dig Dis Sci,1980
5. Molecular aspects of disaccharidase deficiencies;Sterchi;Baillieres Clin Gastroenterol,1990
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1. Congenital Sucrase-isomaltase Deficiency: A Novel Compound Heterozygous Mutation Causing Aberrant Protein Localization;Journal of Pediatric Gastroenterology & Nutrition;2017-05
2. Molecular pathogenicity of novel sucrase-isomaltase mutations found in congenital sucrase-isomaltase deficiency patients;Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease;2017-03
3. Nutrient Digestion, Absorption, and Sensing;Yamada' s Textbook of Gastroenterology;2015-11-27
4. Congenital sucrase–isomaltase deficiency: A case report;GE Portuguese Journal of Gastroenterology;2014-11
5. Enteropathies Associated with Chronic Diarrhea and Malabsorption in Childhood;Pathology of Pediatric Gastrointestinal and Liver Disease;2014
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