RenalTube: a network tool for clinical and genetic diagnosis of primary tubulopathies-Reference-Cited by-同舟云学术

RenalTube: a network tool for clinical and genetic diagnosis of primary tubulopathies

Published:2013-02-07 Issue:6 Volume:172 Page:775-780
ISSN:0340-6199
Container-title:European Journal of Pediatrics
language:en
Short-container-title:Eur J Pediatr

Author:

Mejía Natalia, ,Santos Fernando,Claverie-Martín Félix,García-Nieto Víctor,Ariceta Gema,Castaño Luis

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Link

http://link.springer.com/content/pdf/10.1007/s00431-013-1934-6.pdf

Reference8 articles.

1. Aymé S, Schmidtke J (2007) Networking for rare diseases: a necessity for Europe. Bundesgesundheitsbl Gesundheitsforsch Gesundheitsschutz 50:1477–1483. doi: 10.1007/s00103-007-0381-9

2. Centro de Referencia Estatal de Atención a Personas con Enfermedades Raras (2009). Available at http://www.creenfermedadesraras.es/creer_01/auxiliares/er/index.htm . (Archived by WebCite® at http://www.webcitation.org/6677Cht5O ) Accessed 12 March 2012.

3. Chadha V, Alon US (2009) Hereditary renal tubular disorders. Semin Nephrol 29:399–41. doi: 10.1016/j.semnephrol.2009.03.013

4. Devuyst O, Meij I, Jeunemaitre X et al (2009) EUNEFRON consortium. EUNEFRON, the European Network for the Study of Orphan Nephropathies. Nephrol Dial Transplant 24:2011–2015. doi: 10.1093/ndt/gfp095

5. Foster BJ, Warady BA (2009) Clinical research in pediatric nephrology: challenges, and strategies to address them. J Nephrol 22:685–693

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