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: Atypical hemolytic uremic syndrome: telling the difference between H and Y.
    Author: Goicoechea de Jorge E, Pickering MC.
    Journal: Kidney Int; 2010 Oct; 78(8):721-3. PubMed ID: 20877372.
    Abstract:
    Mutations in the complement factor H (CFH) gene are frequently associated with atypical hemolytic uremic syndrome (aHUS). Hakobyan et al. have developed novel reagents that can rapidly determine the contribution of each CFH allele to the total plasma CFH pool, showing that low-expression CFH alleles are important risk factors for the development of aHUS. These reagents represent a significant contribution to the techniques used to determine susceptibility factors among individuals with aHUS.
    [Abstract] [Full Text] [Related] [New Search]