Systematic reassessment of reported variants in individuals with suspicion of Alport spectrum disorder reveals a high rate of ambiguous results. [PDF]
Riedhammer KM +9 more
europepmc +1 more source
Multiscale molecular modeling-directed ROS-responsive nanotherapy for dual-axis regulation of fibrotic and inflammatory signaling in alport nephropathy. [PDF]
Choi HS +11 more
europepmc +1 more source
Changes in bone characteristics precede serum mineral deterioration in a mouse model of early stage chronic kidney disease. [PDF]
Verlinden L +3 more
europepmc +1 more source
Alport: Renaming an Extended Clinical Spectrum. [PDF]
Lennon R +4 more
europepmc +1 more source
Sequential sequencing reveals the architecture and complexity of genomic variants in patients with Alport syndrome. [PDF]
Di H +11 more
europepmc +1 more source
Phenotype of autosomal dominant Alport syndrome with a likely pathogenic heterozygous variant in the COL4A3 gene (Gly366Arg) and incidental teratozoospermia: A case report. [PDF]
Martín Moreno V +5 more
europepmc +1 more source
Unanswered Questions About Microscopic Hematuria With Tubulopathy. [PDF]
Neild GH +9 more
europepmc +1 more source
Systematic Review of IgA Nephropathy Coexisting With Alport Syndrome. [PDF]
Ying D +7 more
europepmc +1 more source
Modulation of the Apolipoprotein M/S1PR4 Pathway Reduces Podocyte Lipid Overload in Alport Syndrome via Distinct Autophagy and Efflux Mechanisms. [PDF]
Tolerico M +14 more
europepmc +1 more source
Sodium-Glucose Cotransporter-2-inhibitors in Adult Patients With Alport Syndrome. [PDF]
Toso D +12 more
europepmc +1 more source

