Nephrology, Dialysis, Transplantation, 0931-0509

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  1. Calciprotein particle inhibition explains magnesiummediated protection against vascular calcification

    ter Braake, A., Eelderink, C., Zeper, L., Pasch, A., Bakker, S., de Borst, M., Hoenderop, J. & de Baaij, J. H. F., 16-Aug-2019, (Accepted/In press) In : Nephrology Dialysis Transplantation.

    Research output: Contribution to journalArticleAcademicpeer-review

  2. Role of properdin in complement-mediated kidney diseases

    COMBAT Consortium, van Essen, M. F., Ruben, J. M., de Vries, A. P. J. & van Kooten, C., May-2019, In : Nephrology Dialysis Transplantation. 34, 5, p. 742-750 9 p.

    Research output: Contribution to journalReview articleAcademicpeer-review

  3. Antenatal Bartter syndrome with sensorineural deafness: refinement of the locus on chromosome 1p31

    Vollmer, M., Jeck, N., Lemmink, H. H., Vargas, R., Feldmann, D., Konrad, M., Beekmann, F., van Den Heuvel, L. P., Deschenes, G., Guay-Woodford, L. M., Antignac, C., Seyberth, H. W., Hildebrandt, F. & Knoers, N. V., Jul-2000, In : Nephrology, Dialysis, Transplantation. 15, 7, p. 970-4 5 p.

    Research output: Contribution to journalArticleAcademicpeer-review

  4. Autosomal recessive hypophosphataemic rickets with hypercalciuria is not caused by mutations in the type II renal sodium/phosphate cotransporter gene

    van den Heuvel, L., Op de Koul, K., Knots, E., Knoers, N. & Monnens, L., Jan-2001, In : Nephrology, Dialysis, Transplantation. 16, 1, p. 48-51 4 p.

    Research output: Contribution to journalArticleAcademicpeer-review

  5. Exclusion of mutations in FXYD2, CLDN16 and SLC12A3 in two families with primary renal Mg2+ loss

    Meij, I. C., van den Heuvel, L. P. W. J., Hemmes, S., van der Vliet, W. A., Willems, J. L., Monnens, L. A. H. & Knoers, N. V. A. M., 2003, In : Nephrology, Dialysis, Transplantation. 18, 3, p. 512-6 5 p.

    Research output: Contribution to journalArticleAcademicpeer-review

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