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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Dettagli Bibliografici
Pubblicato in:BMC Nephrol
Autori principali: 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
Natura: Artigo
Lingua:Inglês
Pubblicazione: BioMed Central 2015
Soggetti:
Study Protocol
Accesso online: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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