Search Results - "Volokhina, E.B."

Genotype‐phenotype correlations of low‐frequency variants in the complement system in renal disease and age‐related macular degeneration by Geerlings, M.J., Volokhina, E.B., de Jong, E.K., van de Kar, N., Pauper, M., Hoyng, C.B., van den Heuvel, L.P., den Hollander, A.I.

“…Genetic alterations in the complement system have been linked to a variety of diseases, including atypical hemolytic uremic syndrome (aHUS), C3 glomerulopathy…”
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Mutations in the CFHR5 gene and in genes encoding components of the membrane attack complex in patients with atypical hemolytic uremic syndrome by Westra, D., Volokhina, E.B., Klaasen, A., Held, N.M., van de Kar, N.C.A.J., van den Heuvel, L.P.W.J.

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Shiga-like toxin upregulates production of C3 mRNA and protein in human endothelial cells by Volokhina, E.B., Vos, A., van der Velden, T., Westra, D., van de Kar, N.C., van den Heuvel, L.P.

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Novel DNA alterations in FCN1 and FCN2 genes in atypical HUS patients by Volokhina, E.B., Westra, D., Spoelstra, A., van de Kar, N.C., van den Heuvel, L.P.

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Several genetic aberrations in different complement genes in a patient with dense deposit disease by Westra, D., van der Deure, J., Volokhina, E.B., van den Heuvel, L.P.W.J., van de Kar, N.C.A.J.

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