Rationale, design and objectives of ARegPKD, a European ARPKD registry study

BACKGROUND: Autosomal recessive polycystic kidney disease (ARPKD) is a rare but frequently severe disorder that is typically characterized by cystic kidneys and congenital hepatic fibrosis but displays pronounced phenotypic heterogeneity. ARPKD is among the most important causes for pediatric end st...

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Bibliografische gegevens
Gepubliceerd in:BMC Nephrol
Hoofdauteurs: Ebner, Kathrin, Feldkoetter, Markus, Ariceta, Gema, Bergmann, Carsten, Buettner, Reinhard, Doyon, Anke, Duzova, Ali, Goebel, Heike, Haffner, Dieter, Hero, Barbara, Hoppe, Bernd, Illig, Thomas, Jankauskiene, Augustina, Klopp, Norman, König, Jens, Litwin, Mieczyslaw, Mekahli, Djalila, Ranchin, Bruno, Sander, Anja, Testa, Sara, Weber, Lutz Thorsten, Wicher, Dorota, Yuzbasioglu, Ayse, Zerres, Klaus, Dötsch, Jörg, Schaefer, Franz, Liebau, Max Christoph
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: BioMed Central 2015
Onderwerpen:
Study Protocol
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4359504/
https://ncbi.nlm.nih.gov/pubmed/25886171
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12882-015-0002-z
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