These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
25. Index of suspicion. Case 3. Congenital sucrase-isomaltase deficiency. Mahant S; Friedman J Pediatr Rev; 2000 Jan; 21(1):20, 24-5. PubMed ID: 10702073 [No Abstract] [Full Text] [Related]
26. Congenital sucrase-isomaltase deficiency arising from cleavage and secretion of a mutant form of the enzyme. Jacob R; Zimmer KP; Schmitz J; Naim HY J Clin Invest; 2000 Jul; 106(2):281-7. PubMed ID: 10903344 [TBL] [Abstract][Full Text] [Related]
27. Sucrase-isomaltase regulation by dietary sucrose in the rat. Cézard JP; Broyart JP; Cuisinier-Gleizes P; Mathieu H Gastroenterology; 1983 Jan; 84(1):18-25. PubMed ID: 6847846 [No Abstract] [Full Text] [Related]
28. Compound heterozygous mutations affect protein folding and function in patients with congenital sucrase-isomaltase deficiency. Alfalah M; Keiser M; Leeb T; Zimmer KP; Naim HY Gastroenterology; 2009 Mar; 136(3):883-92. PubMed ID: 19121318 [TBL] [Abstract][Full Text] [Related]
33. Performance of empirical and model-based classifiers for detecting sucrase-isomaltase inhibition using the Van Wyk H; Lee GO; Schillinger RJ; Edwards CA; Morrison DJ; Brouwer AF J Breath Res; 2024 Sep; 18(4):. PubMed ID: 39197471 [TBL] [Abstract][Full Text] [Related]
34. Human small intestinal sucrase-isomaltase: different binding patterns for malto- and isomaltooligosaccharides. Heymann H; Breitmeier D; Günther S Biol Chem Hoppe Seyler; 1995 Apr; 376(4):249-53. PubMed ID: 7626234 [TBL] [Abstract][Full Text] [Related]
35. Sucrase-isomaltase in colon cancers: an example of re-expression of a foetal enzyme with associated blood group antigens. Chantret I Ann Inst Pasteur Immunol; 1987; 138(6):901-5. PubMed ID: 3329917 [No Abstract] [Full Text] [Related]
37. Use of a monoclonal antibody to sucrase-isomaltase for evaluation of the columnar cuff after stapled restorative proctocolectomy. Thompson-Fawcett MW; McC Mortensen NJ; Jewel DP; Warren BF Dis Colon Rectum; 2007 Sep; 50(9):1428-35. PubMed ID: 17665257 [TBL] [Abstract][Full Text] [Related]
38. Novel mutations in the human sucrase-isomaltase gene (SI) that cause congenital carbohydrate malabsorption. Sander P; Alfalah M; Keiser M; Korponay-Szabo I; Kovács JB; Leeb T; Naim HY Hum Mutat; 2006 Jan; 27(1):119. PubMed ID: 16329100 [TBL] [Abstract][Full Text] [Related]
39. [Structure and evolution of mammalian maltase-glucoamylase and sucrase-isomaltase genes]. Naumov DG Mol Biol (Mosk); 2007; 41(6):1056-68. PubMed ID: 18318124 [TBL] [Abstract][Full Text] [Related]
40. Homozygosity mapping of the gene for alkaptonuria to chromosome 3q2. Pollak MR; Chou YH; Cerda JJ; Steinmann B; La Du BN; Seidman JG; Seidman CE Nat Genet; 1993 Oct; 5(2):201-4. PubMed ID: 8252048 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]