Results 111 to 120 of about 3,403 (162)

Autosomal Type IV Collagen Genes Display Sex Differences in Genetic Risk for Hematuria. [PDF]

Kidney Int Rep
Lona-Durazo F, Dinsmore IR, McNulty MT, Sampson MG, Forest L, Mirshahi T, Chang AR, Paterson AD, Barua M, Gagliano Taliun SA.   +9 more
europepmc   +1 more source

Alport: Renaming an Extended Clinical Spectrum. [PDF]

J Am Soc Nephrol
Lennon R, Miner JH, Savige J, Weinstock BA, Gear S.   +4 more
europepmc   +1 more source

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

Nat Commun
Di H, You Z, Wang L, Sun Q, Zhang J, Lv Q, Wang P, Lai Z, Wang G, Zheng C, Gong L, Liu Z.   +11 more
europepmc   +1 more source

Precision Medicine in Pediatric Nephrology: From Shared Clinical Phenotypes to Genotype-Guided Diagnosis and Management. [PDF]

Genes (Basel)
Dotis J, Printza N.
europepmc   +1 more source

Genetic diagnosis of hereditary kidney disease in pediatric patients through whole-exome sequencing and mitochondrial DNA analysis. [PDF]

Kidney Res Clin Pract
Oh J, Lee K, Won D, Lee YM, Shin JI.
europepmc   +1 more source

Unanswered Questions About Microscopic Hematuria With Tubulopathy. [PDF]

Kidney Int Rep
Neild GH, Oygar DD, Behlul A, Ataçi S, Yükseliş M, Özadalı S, Ozdemir F, Kazan HH, Gale DP, Gurkan C.   +9 more
europepmc   +1 more source

Thin Glomerular Basement Membrane Phenotypes With No Identified Pathogenic <i>COL4A3/A4/A5</i> Variant. [PDF]

Kidney Int Rep
Riella CV, Colombo DA, Rennke HG, Weins A, Rosen S, Lin MH, Suhas T, Stillman IE, Heher YK, Bianchi G, Zivna M, Bleyer AJ, Kmoch S, Lu W, Miner JH, Czarnecki PG.   +15 more
europepmc   +1 more source

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

Kidney Int Rep
Toso D, Cinquina V, Econimo L, Cortinovis R, Zeni L, Tornambè V, Dordoni C, Ritelli M, Savoldi G, Mazza C, Scolari F, Alberici F, Izzi C.   +12 more
europepmc   +1 more source

Hearing loss and truncating variants in Alport syndrome. [PDF]

Kidney Res Clin Pract
Yim HE.
europepmc   +1 more source

Genetic heterogeneity correlated with phenotypic variability in 6 Chinese families with Alport syndrome. [PDF]

Front Genet
Gao J, Zhou H, Zhang L, Su Z, Liu S.
europepmc   +1 more source