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.


PUBMED FOR HANDHELDS

Search MEDLINE/PubMed


  • Title: [Malabsorption syndrome due to membrane transporter abnormality in absorptive epithelial cells].
    Author: Bamba T, Sasaki M.
    Journal: Nihon Rinsho; 1996 Mar; 54(3):782-7. PubMed ID: 8904237.
    Abstract:
    Pathogenesis, clinical features and diagnosis of malabsorption syndrome caused by membrane transporter abnormality of absorptive epithelial cells, such as glucose-galactose malabsorption or inherited amino acid transporter abnormality, are reviewed in this paper. It is rare for us to examine the patients with these diseases, but they are important for study of mechanisms of membrane digestion and membrane transporter in absorptive epithelial cells. Recent advances in molecular biology or genetics have made us details for the etiology of these diseases and may result in the development for new therapy.
    [Abstract] [Full Text] [Related] [New Search]