Cargando…
Pierson Syndrome in an Infant With Congenital Nephrotic Syndrome and Unique Brain Pathology
Autores principales: | Hiser, Wesley, Thirumala, Vani, Wang, Jason, Gillespie, Robert, Bedri, Badreldin, Zhou, Xin Jin |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7710838/ https://www.ncbi.nlm.nih.gov/pubmed/33305134 http://dx.doi.org/10.1016/j.ekir.2020.09.023 |
Ejemplares similares
-
Disarranged Sphingolipid Metabolism From Sphingosine-1-Phosphate Lyase Deficiency Leads to Congenital Nephrotic Syndrome
por: Taylor, Veronica A., et al.
Publicado: (2019) -
Ischemic Stroke of Possible Embolic Etiology Associated With Nephrotic Syndrome
por: Roy, Claudie, et al.
Publicado: (2017) -
Extreme Renal Pathology in Alagille Syndrome
por: Bissonnette, Mei Lin Z., et al.
Publicado: (2016) -
Mitochondrial Neurogastrointestinal Encephalomyopathy Causing Fanconi Syndrome
por: Razzaq, Ansa, et al.
Publicado: (2022) -
Alport Syndrome With Kidney Cysts Is Still Alport Syndrome
por: Savige, Judy, et al.
Publicado: (2021)