Phenotypic Observations by the CSID Dietary and Medical Support Group
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Gastroenterology,Pediatrics, Perinatology and Child Health
Reference12 articles.
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2. 13C-breath tests for sucrose digestion in congenital sucrase isomaltase-deficient and sacrosidase-supplemented patients.;Robayo-Torres;J Pediatr Gastroenterol Nutr,2009
3. Novel mutations in the human sucrase-isomaltase gene (SI) that cause congenital carbohydrate malabsorption.;Sander;Hum Mutat,2006
4. Evaluation of liquid yeast-derived sucrase enzyme replacement in patients with sucrase-isomaltase deficiency.;Treem;Gastroenterology,1993
5. Immunoelectrophoretic studies on human small intestinal brush border proteins. The residual isomaltase in sucrose intolerant patients.;Skovbjerg;Pediatr Res,1981
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1. Diet management in congenital diarrheas and enteropathies – general concepts and disease-specific approach, a narrative review;The American Journal of Clinical Nutrition;2024-07
2. Diet and Management of Diarrhea;Indian Journal of Pediatrics;2023-07-22
3. Improved Starch Digestion of Sucrase-deficient Shrews Treated With Oral Glucoamylase Enzyme Supplements;Journal of Pediatric Gastroenterology & Nutrition;2017-08
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