Clinical courses and complications of young adults with Autosomal Recessive Polycystic Kidney Disease (ARPKD)

Autosomal recessive polycystic kidney disease (ARPKD) is a severe pediatric hepatorenal disorder with pronounced phenotypic variability. A substantial number of patients with early diagnosis reaches adulthood and some patients are not diagnosed until adulthood. Yet, clinical knowledge about adult AR...

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Detaylı Bibliyografya
Yayımlandı:Sci Rep
Asıl Yazarlar: Burgmaier, Kathrin, Kilian, Samuel, Bammens, Bert, Benzing, Thomas, Billing, Heiko, Büscher, Anja, Galiano, Matthias, Grundmann, Franziska, Klaus, Günter, Mekahli, Djalila, Michel-Calemard, Laurence, Milosevski-Lomic, Gordana, Ranchin, Bruno, Sauerstein, Katja, Schaefer, Susanne, Shroff, Rukshana, Sterenborg, Rosalie, Verbeeck, Sarah, Weber, Lutz T., Wicher, Dorota, Wühl, Elke, Dötsch, Jörg, Schaefer, Franz, Liebau, Max C.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Nature Publishing Group UK 2019
Konular:
Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6538621/
https://ncbi.nlm.nih.gov/pubmed/31138820
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-019-43488-w
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