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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...
Autores principales: | Li, Baihong, Zhang, Yanqin, Wang, Fang, Nair, Viji, Ding, Fangrui, Xiao, Huijie, Yao, Yong, Kretzler, Matthias, Ju, Wenjun, Ding, Jie |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2018
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Materias: | |
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 |
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