Cargando…
Genetic studies of IgA nephropathy: past, present, and future
Immunoglobulin A nephropathy (IgAN) is the most common form of primary glomerulonephritis worldwide and an important cause of kidney disease in young adults. Highly variable clinical presentation and outcome of IgAN suggest that this diagnosis may encompass multiple subsets of disease that are not d...
Autores principales: | Kiryluk, Krzysztof, Julian, Bruce A., Wyatt, Robert J., Scolari, Francesco, Zhang, Hong, Novak, Jan, Gharavi, Ali G. |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Springer-Verlag
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2937145/ https://www.ncbi.nlm.nih.gov/pubmed/20386929 http://dx.doi.org/10.1007/s00467-010-1500-7 |
Ejemplares similares
-
The level of galactose-deficient IgA1 in the sera of patients with IgA nephropathy is associated with disease progression
por: Zhao, Na, et al.
Publicado: (2012) -
Inhibition of STAT3 Signaling Reduces IgA1 Autoantigen Production in IgA Nephropathy
por: Yamada, Koshi, et al.
Publicado: (2017) -
A Panel of Serum Biomarkers Differentiates IgA Nephropathy from Other Renal Diseases
por: Yanagawa, Hiroyuki, et al.
Publicado: (2014) -
Type IV Collagen Mutations in Familial IgA Nephropathy
por: Li, Yifu, et al.
Publicado: (2020) -
New developments in the genetics, pathogenesis, and therapy of IgA nephropathy
por: Magistroni, Riccardo, et al.
Publicado: (2015)