Clinical predictors of escalating care in hepatic and renal cyst infection in autosomal dominant polycystic kidney and liver disease

Autor: Marten Lantinga, Sevaux, R. G. L., Gevers, T. J. G., Oyen, W. J. G., Fijter, J. W., Soonawala, D., Zietse, R., Salih, M., Casteleijn, N. F., Spithoven, E. M., Meijer, E., Gansevoort, R. T., Drenthl, J. P. H.

Publikováno v: The Netherlands Journal of Medicine, 76(5), 226-234. van Zuiden Communications BV.
Netherlands Journal of Medicine, 76(5), 226-234. Van Zuiden Communications
Publons

BACKGROUND: Cyst infection may occur in autosomal dominant polycystic kidney disease (ADPKD) and autosomal dominant polycystic liver disease (ADPLD). Antimicrobial agents often fail to control infection, leading to invasive action. We aimed to identi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::139a9eff468439f692f3e0e18498fcf5
https://research.rug.nl/en/publications/bc360867-bdb4-4b82-9f52-c49ea5d76ff4

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[Unexpected metal in the pelvis].

Autor: Mohede DCJ; Afdeling Urologie, Universitair Medisch Centrum Groningen, Groningen., Casteleijn NF, Cauberg ECC

Publikováno v: Nederlands tijdschrift voor geneeskunde [Ned Tijdschr Geneeskd] 2017; Vol. 161, pp. D1699.