Urinary epidermal growth factor as a prognostic marker for the progression of Alport syndrome in children

BACKGROUND: Alport syndrome is a rare hereditary kidney disease manifested with progressive renal failure. Considerable variation exists in terms of disease progression among patients with Alport syndrome. Identification of patients at high risk of rapid progression remains an unmet need. Urinary ep...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Baihong, Zhang, Yanqin, Wang, Fang, Nair, Viji, Ding, Fangrui, Xiao, Huijie, Yao, Yong, Kretzler, Matthias, Ju, Wenjun, Ding, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2018
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6132884/
https://www.ncbi.nlm.nih.gov/pubmed/29948307
http://dx.doi.org/10.1007/s00467-018-3988-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6132884/
https://www.ncbi.nlm.nih.gov/pubmed/29948307
http://dx.doi.org/10.1007/s00467-018-3988-1

Ejemplares similares