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Journal Abstract Search

129 related items for PubMed ID: 1256470

  • 1. Sucrase-isomaltase deficiency. Absence of an inactive enzyme variant.
    Gray GM, Conklin KA, Townley RR.
    N Engl J Med; 1976 Apr 01; 294(14):750-3. PubMed ID: 1256470
    [Abstract] [Full Text] [Related]

  • 2. Absence of brush border sucrase-isomaltase complex in congenital sucrose intolerance.
    Schmitz J, Commegrain C, Maestracci D, Rey J.
    Biomedicine; 1974 Nov 20; 21(11):440-3. PubMed ID: 4464992
    [No Abstract] [Full Text] [Related]

  • 3. Letter: Gene frequency of sucrase-isomaltase deficiency.
    Hoegerman SF, Hoegerman G.
    N Engl J Med; 1976 Jul 29; 295(5):284. PubMed ID: 934201
    [No Abstract] [Full Text] [Related]

  • 4. Letter: Sucrase-isomaltase deficiency.
    Schmitz J, Rey J, Hadorn B.
    N Engl J Med; 1976 Oct 14; 295(16):902-3. PubMed ID: 958299
    [No Abstract] [Full Text] [Related]

  • 5. [Congenital saccharase-isomaltase defect--diagnostic difficulties].
    Kovács JB, Lörincz M, Sashegyi J, Marton A, Simon K.
    Orv Hetil; 1989 Nov 26; 130(48):2577-82. PubMed ID: 2513545
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  • 7. A study of the molecular pathology of sucrase-isomaltase deficiency. A defect in the intracellular processing of the enzyme.
    Lloyd ML, Olsen WA.
    N Engl J Med; 1987 Feb 19; 316(8):438-42. PubMed ID: 3807985
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  • 9. 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 19; 136(3):883-92. PubMed ID: 19121318
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  • 11. The intestinal brush border membrane in diabetes. Studies of sucrase-isomaltase metabolism in rats with streptozotocin diabetes.
    Olsen WA, Korsmo H.
    J Clin Invest; 1977 Jul 19; 60(1):181-8. PubMed ID: 141462
    [Abstract] [Full Text] [Related]

  • 12. 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 19; 27(1):119. PubMed ID: 16329100
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  • 14. Editorial: Genetic heterogeneity of human enzymes.
    Nyhan WL.
    N Engl J Med; 1976 Apr 01; 294(14):781-2. PubMed ID: 1256473
    [No Abstract] [Full Text] [Related]

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  • 16. [Primary saccharose-isomaltose deficit: a 20-year case load].
    Prieto Bozano G, Miralles Adárraga T, Carrasco Gandía S, Lama Moré R, Codoceo Alquinta R, Polanco Allué I.
    An Esp Pediatr; 1990 Apr 01; 32(4):317-20. PubMed ID: 2368994
    [Abstract] [Full Text] [Related]

  • 17. Immunoelectrophoretic studies on human small intestinal brush border proteins. The residual isomaltase in sucrose intolerant patients.
    Skovbjerg H, Krasilnikoff PA.
    Pediatr Res; 1981 Mar 01; 15(3):214-8. PubMed ID: 7220143
    [Abstract] [Full Text] [Related]

  • 18. 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 01; 106(2):281-7. PubMed ID: 10903344
    [Abstract] [Full Text] [Related]

  • 19. Sucrase-isomaltase (palatinase) deficiency diagnosed during adulthood.
    Ringrose RE, Preiser H, Welsh JD.
    Dig Dis Sci; 1980 May 01; 25(5):384-7. PubMed ID: 7371476
    [No Abstract] [Full Text] [Related]

  • 20. Studies on intestinal digestion of starch in children with congenital deficiency of sucrase and isomaltase activity.
    Auricchio S, Ciccimarra F, Jos J, Rey F, Moauro L, Rey J.
    Acta Paediatr Scand; 1971 May 01; 60(3):364. PubMed ID: 5579866
    [No Abstract] [Full Text] [Related]

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