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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...
Autores principales: | 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. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6538621/ https://www.ncbi.nlm.nih.gov/pubmed/31138820 http://dx.doi.org/10.1038/s41598-019-43488-w |
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