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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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Study Protocol
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4359504/
https://www.ncbi.nlm.nih.gov/pubmed/25886171
http://dx.doi.org/10.1186/s12882-015-0002-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4359504/
https://www.ncbi.nlm.nih.gov/pubmed/25886171
http://dx.doi.org/10.1186/s12882-015-0002-z

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