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American Journal of Medical Genetics. Part A|August 7, 2018
Mutations in WDR4 as a new cause of Galloway-Mowat syndromeDaniela A Braun, Shirlee Shril, Aditi Sinha, et al.Kidney International Reports|October 27, 2025
Exome Sequencing in Saudi Arabian Pediatric Kidney Disease Single-Center CohortKatharina Lemberg, Mohamed A Shalaby, Elena Zion, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|March 14, 2018
Genetic variants in the LAMA5 gene in pediatric nephrotic syndromeDaniela A Braun, Jillian K Warejko, Shazia Ashraf, et al.American Journal of Medical Genetics. Part A|August 2, 2021
Exome survey of individuals affected by VATER/VACTERL with renal phenotypes identifies phenocopies and novel candidate genesCaroline M Kolvenbach, Amelie T van der Ven, Franziska Kause, et al.Journal of the American Society of Nephrology : JASN|July 1, 2018
GAPVD1 and ANKFY1 Mutations Implicate RAB5 Regulation in Nephrotic SyndromeTobias Hermle, Ronen Schneider, David Schapiro, et al.Nature Communications|March 14, 2019
Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactylyNajim Lahrouchi, Aman George, Ilham Ratbi, et al.Kidney International Reports|February 22, 2021
Recessive Mutations in SYNPO2 as a Candidate of Monogenic Nephrotic SyndromeYouying Mao, Ronen Schneider, Peter F M van der Ven, et al.American Journal of Human Genetics|November 24, 2020
DAAM2 Variants Cause Nephrotic Syndrome via Actin DysregulationRonen Schneider, Konstantin Deutsch, Gregory J Hoeprich, et al.Journal of the American Society of Nephrology : JASN|January 19, 2019
Whole-Exome Sequencing Enables a Precision Medicine Approach for Kidney Transplant RecipientsNina Mann, Daniela A Braun, Kassaundra Amann, et al.Pediatric Nephrology (Berlin, Germany)|January 23, 2026
Identification of monogenic variants in steroid-resistant and steroid-sensitive nephrotic syndromeBshara Mansour, Katharina Lemberg, Ronen Schneider, et al.Pageof 5