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Journal Abstract Search

147 related items for PubMed ID: 22843301

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  • 7. Bitterness of glucose/galactose: novel mutations in the SLC5A1 gene.
    Pode-Shakked B, Reish O, Aktuglu-Zeybek C, Kesselman D, Dekel B, Bujanover Y, Anikster Y.
    J Pediatr Gastroenterol Nutr; 2014 Jan; 58(1):57-60. PubMed ID: 24048166
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  • 8. Molecular basis for glucose-galactose malabsorption.
    Wright EM, Turk E, Martin MG.
    Cell Biochem Biophys; 2002 Jan; 36(2-3):115-21. PubMed ID: 12139397
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  • 13. Nephrocalcinosis in glucose-galactose malabsorption: nephrocalcinosis and proximal tubular dysfunction in a young infant with a novel mutation of SGLT1.
    Soylu OB, Ecevit C, Altinöz S, Oztürk AA, Temizkan AK, Maeda M, Kasahara M.
    Eur J Pediatr; 2008 Dec; 167(12):1395-8. PubMed ID: 18288487
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  • 18. Structural insights into genetic variants of Na(+)/glucose cotransporter SGLT1 causing glucose-galactose malabsorption: vSGLT as a model structure.
    Raja M, Kinne RK.
    Cell Biochem Biophys; 2012 Jun; 63(2):151-8. PubMed ID: 22383112
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  • 19. I. Glucose galactose malabsorption.
    Wright EM.
    Am J Physiol; 1998 Nov; 275(5):G879-82. PubMed ID: 9815014
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  • 20. A novel mutation of Na+/glucose cotransporter in a Turkish newborn with congenital glucose-galactose malabsorption.
    Gok F, Aydin HI, Kurt I, Gokcay E, Maeda M, Kasahara M.
    J Pediatr Gastroenterol Nutr; 2005 Apr; 40(4):508-11. PubMed ID: 15795603
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