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Journal Abstract Search

366 related items for PubMed ID: 1848001

  • 1. Inherited selective intestinal cobalamin malabsorption and cobalamin deficiency in dogs.
    Fyfe JC, Giger U, Hall CA, Jezyk PF, Klumpp SA, Levine JS, Patterson DF.
    Pediatr Res; 1991 Jan; 29(1):24-31. PubMed ID: 1848001
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  • 2. Selective cobalamin malabsorption and the cobalamin-intrinsic factor receptor.
    Gräsbeck R.
    Acta Biochim Pol; 1997 Jan; 44(4):725-33. PubMed ID: 9584852
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  • 5. Serum cobalamin, urine methylmalonic acid, and plasma total homocysteine concentrations in Border Collies and dogs of other breeds.
    Lutz S, Sewell AC, Bigler B, Riond B, Reusch CE, Kook PH.
    Am J Vet Res; 2012 Aug; 73(8):1194-9. PubMed ID: 22849680
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  • 6. An exon 53 frameshift mutation in CUBN abrogates cubam function and causes Imerslund-Gräsbeck syndrome in dogs.
    Fyfe JC, Hemker SL, Venta PJ, Fitzgerald CA, Outerbridge CA, Myers SL, Giger U.
    Mol Genet Metab; 2013 Aug; 109(4):390-6. PubMed ID: 23746554
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  • 7. Daily oral cyanocobalamin supplementation in Beagles with hereditary cobalamin malabsorption (Imerslund-Gräsbeck syndrome) maintains normal clinical and cellular cobalamin status.
    Kook PH, Hersberger M.
    J Vet Intern Med; 2019 Mar; 33(2):751-757. PubMed ID: 30554416
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  • 8. Failure to thrive and life-threatening complications due to inherited selective cobalamin malabsorption effectively managed in a juvenile Australian shepherd dog.
    Gold AJ, Scott MA, Fyfe JC.
    Can Vet J; 2015 Oct; 56(10):1029-34. PubMed ID: 26483576
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  • 9. Prospective long-term evaluation of parenteral hydroxocobalamin supplementation in juvenile beagles with selective intestinal cobalamin malabsorption (Imerslund-Gräsbeck syndrome).
    Kook PH, Reusch CE, Hersberger M.
    J Vet Intern Med; 2018 May; 32(3):1033-1040. PubMed ID: 29572946
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  • 11. Imerslund-Gräsbeck syndrome (selective vitamin B(12) malabsorption with proteinuria).
    Gräsbeck R.
    Orphanet J Rare Dis; 2006 May 19; 1():17. PubMed ID: 16722557
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  • 14. Vitamin B12 in health and disease: part I--inherited disorders of function, absorption, and transport.
    Kapadia CR.
    Gastroenterologist; 1995 Dec 19; 3(4):329-44. PubMed ID: 8775094
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  • 15. Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns.
    Tanner SM, Sturm AC, Baack EC, Liyanarachchi S, de la Chapelle A.
    Orphanet J Rare Dis; 2012 Aug 28; 7():56. PubMed ID: 22929189
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  • 16. Systemic Scedosporium prolificans infection in an 11-month-old Border collie with cobalamin deficiency secondary to selective cobalamin malabsorption (canine Imerslund-Gräsbeck syndrome).
    Erles K, Mugford A, Barfield D, Leeb T, Kook PH.
    J Small Anim Pract; 2018 Apr 28; 59(4):253-256. PubMed ID: 28390190
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  • 17. Cobalamin deficiency associated with erythroblastic anemia and methylmalonic aciduria in a border collie.
    Morgan LW, McConnell J.
    J Am Anim Hosp Assoc; 1999 Apr 28; 35(5):392-5. PubMed ID: 10493414
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  • 20. Correction of cobalamin malabsorption in pancreatic insufficiency with a cobalamin analogue that binds with high affinity to R protein but not to intrinsic factor. In vivo evidence that a failure to partially degrade R protein is responsible for cobalamin malabsorption in pancreatic insufficiency.
    Allen RH, Seetharam B, Allen NC, Podell ER, Alpers DH.
    J Clin Invest; 1978 Jun 28; 61(6):1628-34. PubMed ID: 659618
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