Results 131 to 140 of about 4,891 (195)

Systematic reassessment of reported variants in individuals with suspicion of Alport spectrum disorder reveals a high rate of ambiguous results. [PDF]

open access: yesEur J Hum Genet
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]

open access: yesJ Nanobiotechnology
Choi HS   +11 more
europepmc   +1 more source

Alport: Renaming an Extended Clinical Spectrum. [PDF]

open access: yesJ Am Soc Nephrol
Lennon R   +4 more
europepmc   +1 more source

Sequential sequencing reveals the architecture and complexity of genomic variants in patients with Alport syndrome. [PDF]

open access: yesNat Commun
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]

open access: yesAn Sist Sanit Navar
Martín Moreno V   +5 more
europepmc   +1 more source

Unanswered Questions About Microscopic Hematuria With Tubulopathy. [PDF]

open access: yesKidney Int Rep
Neild GH   +9 more
europepmc   +1 more source

Systematic Review of IgA Nephropathy Coexisting With Alport Syndrome. [PDF]

open access: yesKidney Int Rep
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]

open access: yesJ Am Soc Nephrol
Tolerico M   +14 more
europepmc   +1 more source

Sodium-Glucose Cotransporter-2-inhibitors in Adult Patients With Alport Syndrome. [PDF]

open access: yesKidney Int Rep
Toso D   +12 more
europepmc   +1 more source

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