A unique evolution of the kidney phenotype in a patient with autosomal recessive Alport syndrome
Author:
Publisher
Elsevier BV
Subject
Pathology and Forensic Medicine
Reference12 articles.
1. Alport's syndrome: a report of 58 cases and a review of the literature;Gubler;Am J Med,1981
2. The Oxford classification of IgA nephropathy: pathology definitions, correlations, and reproducibility;Roberts;Kidney Int,2009
3. A multicenter study of the predictive value of crescents in IgA nephropathy;Haas;J Am Soc Nephrol,2017
4. The 2014 international workshop on Alport syndrome;Miner;Kidney Int,2014
5. COL4A3/COL4A4 mutations and features in individuals with autosomal recessive Alport syndrome;Storey;J Am Soc Nephrol,2013
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1. Abnormal mRNA Splicing Effect of COL4A3 to COL4A5 Unclassified Variants;Kidney International Reports;2023-07
2. Genotype–phenotype correlations and nephroprotective effects of RAAS inhibition in patients with autosomal recessive Alport syndrome;Pediatric Nephrology;2021-03-27
3. An overview of the multi-pronged approach in the diagnosis of Alport syndrome for 22 children in Northeast China;BMC Nephrology;2020-07-23
4. The First COL4A5 Exon 41A Glycine Substitution in a Family With Alport Syndrome;Frontiers in Pediatrics;2020-04-09
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