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Design and Implementation of the Hepatorenal Fibrocystic Disease Core Center Clinical Database: A Centralized Resource for Characterizing Autosomal Recessive Polycystic Kidney Disease and Other Hepatorenal Fibrocystic Diseases

Autosomal recessive polycystic kidney disease (ARPKD) and other hepatorenal fibrocystic diseases (HRFD) are relatively rare recessive disorders that constitute an important set of childhood nephropathies. Little is known about fundamental pathogenesis, and advances toward clinical trials will requir...

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Detalles Bibliográficos
Autores principales: Alzarka, Bakri, Morizono, Hiroki, Bollman, John W., Kim, Dongkyu, Guay-Woodford, Lisa M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5397503/
https://www.ncbi.nlm.nih.gov/pubmed/28473971
http://dx.doi.org/10.3389/fped.2017.00080

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