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Journal Abstract Search

131 related items for PubMed ID: 23103649

  • 1.
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  • 2. Starch digestion and patients with congenital sucrase-isomaltase deficiency.
    Hamaker BR, Lee BH, Quezada-Calvillo R.
    J Pediatr Gastroenterol Nutr; 2012 Nov; 55 Suppl 2():S24-8. PubMed ID: 23103646
    [No Abstract] [Full Text] [Related]

  • 3. Direct starch digestion by sucrase-isomaltase and maltase-glucoamylase.
    Lin AH, Hamaker BR, Nichols BL.
    J Pediatr Gastroenterol Nutr; 2012 Nov; 55 Suppl 2():S43-5. PubMed ID: 23103656
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  • 5. Research progress reported at the 50th Anniversary of the Discovery of Congenital Sucrase-Isomaltase Deficiency Workshop.
    Gilger M, Hamaker B, Nichols BL, Auricchio S, Treem WR, Naim HY, Heine M, Zimmer KP, Jones K, Eskandari R, Pinto BM, Rose DR, Lee BH, Quezada-Calvillo R, Adams B, Roach CM, Ma CX, Baker SS, Slawson MH, Robayo-Torres CC, Chumpitazi BP, Lecea CE, Opekun AR, Uhrich S, Wu Z, Huang JY, Scott CR, Chumpitazi BP, McMeans AR, Scholz D, Shulman RJ, Ao Z, Sterchi EE, Lin AH.
    J Pediatr Gastroenterol Nutr; 2012 Nov; 55 Suppl 2(0 2):S1. PubMed ID: 23103641
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  • 6. 50 years of progress since congenital sucrase-isomaltase deficiency recognition.
    Nichols BL, Auricchio S.
    J Pediatr Gastroenterol Nutr; 2012 Nov; 55 Suppl 2():S2-7. PubMed ID: 23103644
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  • 8. Clinical aspects and treatment of congenital sucrase-isomaltase deficiency.
    Treem WR.
    J Pediatr Gastroenterol Nutr; 2012 Nov; 55 Suppl 2():S7-13. PubMed ID: 23103658
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  • 10. Inhibition of maltase-glucoamylase activity to hydrolyze α-1,4 linkages by the presence of undigested sucrose.
    Lee BH, Quezada-Calvillo R, Nichols BL, Rose DR, Hamaker BR.
    J Pediatr Gastroenterol Nutr; 2012 Nov; 55 Suppl 2():S45-7. PubMed ID: 23103657
    [No Abstract] [Full Text] [Related]

  • 11. Phenotypic observations by the CSID Dietary and Medical Support Group.
    Slawson MH.
    J Pediatr Gastroenterol Nutr; 2012 Nov; 55 Suppl 2():S30-2. PubMed ID: 23103648
    [No Abstract] [Full Text] [Related]

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  • 13. 13C-breath tests for sucrose digestion in congenital sucrase isomaltase-deficient and sacrosidase-supplemented patients.
    Robayo-Torres CC, Opekun AR, Quezada-Calvillo R, Villa X, Smith EO, Navarrete M, Baker SS, Nichols BL.
    J Pediatr Gastroenterol Nutr; 2009 Apr; 48(4):412-8. PubMed ID: 19330928
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  • 16. Differential Effects of Sucrase-Isomaltase Mutants on Its Trafficking and Function in Irritable Bowel Syndrome: Similarities to Congenital Sucrase-Isomaltase Deficiency.
    Husein DM, Rizk S, Naim HY.
    Nutrients; 2020 Dec 22; 13(1):. PubMed ID: 33375084
    [Abstract] [Full Text] [Related]

  • 17. Evaluation of liquid yeast-derived sucrase enzyme replacement in patients with sucrase-isomaltase deficiency.
    Treem WR, Ahsan N, Sullivan B, Rossi T, Holmes R, Fitzgerald J, Proujansky R, Hyams J.
    Gastroenterology; 1993 Oct 22; 105(4):1061-8. PubMed ID: 8405850
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  • 19. Disorders of carbohydrate absorption.
    Harries JT.
    Clin Gastroenterol; 1982 Jan 22; 11(1):17-36. PubMed ID: 7037237
    [No Abstract] [Full Text] [Related]

  • 20. Molecular pathogenicity of novel sucrase-isomaltase mutations found in congenital sucrase-isomaltase deficiency patients.
    Gericke B, Amiri M, Scott CR, Naim HY.
    Biochim Biophys Acta Mol Basis Dis; 2017 Mar 22; 1863(3):817-826. PubMed ID: 28062276
    [Abstract] [Full Text] [Related]

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