Cargando…
The KOUNCIL Consortium: From Genetic Defects to Therapeutic Development for Nephronophthisis
Nephronophthisis (NPH) is the most common monogenic cause of renal failure in children. Treatment options are limited to dialysis and transplantation. Therapeutics to significantly delay or prevent end-stage renal disease (ESRD) in children are currently not available. In the Dutch-Anglo KOUNCIL (Ki...
Autores principales: | Renkema, Kirsten Y., Giles, Rachel H., Lilien, Marc R., Beales, Philip L., Roepman, Ronald, Oud, Machteld M., Arts, Heleen H., Knoers, Nine V. A. M. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5949343/ https://www.ncbi.nlm.nih.gov/pubmed/29868523 http://dx.doi.org/10.3389/fped.2018.00131 |
Ejemplares similares
-
KOUNCIL: Kidney-Oriented Understanding of Correcting Ciliopathies
por: Stokman, M, et al.
Publicado: (2015) -
Clinical and genetic analyses of a Dutch cohort of 40 patients with a nephronophthisis-related ciliopathy
por: Stokman, Marijn F., et al.
Publicado: (2018) -
Current insights into renal ciliopathies: what can genetics teach us?
por: Arts, Heleen H., et al.
Publicado: (2012) -
Non-invasive sources of cells with primary cilia from pediatric and adult patients
por: Ajzenberg, Henry, et al.
Publicado: (2015) -
Many Genes—One Disease? Genetics of Nephronophthisis (NPHP) and NPHP-Associated Disorders
por: Srivastava, Shalabh, et al.
Publicado: (2018)