Showing results (1-10 of 120) with videos related to
Sort By:
Pageof 12
Kidney International|May 31, 2014
Recessive mutations in CAKUT and VACTERL associationRik Westland, Simone Sanna-CherchiGiornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|October 20, 2015
[Genetic Basis of Congenital Anomalies of the Kidney and Urinary Tract]Monica Bodria, Simone Sanna-CherchiPediatric Nephrology (Berlin, Germany)|September 5, 2023
Copy number variation analysis in 138 families with steroid-resistant nephrotic syndrome identifies causal homozygous deletions in PLCE1 and NPHS2 in two familiesDalia Pantel, Nils D Mertens, Ronen Schneider, et al.Experimental Dermatology|June 7, 2019
Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagyLynn Petukhova, Aakash V Patel, Rachel K Rigo, et al.The Journal of Clinical Investigation|January 3, 2018
Genetic basis of human congenital anomalies of the kidney and urinary tractSimone Sanna-Cherchi, Rik Westland, Gian Marco Ghiggeri, et al.The Journal of Clinical Investigation|April 21, 2015
Genomic imbalances in pediatric patients with chronic kidney diseaseMiguel Verbitsky, Simone Sanna-Cherchi, David A Fasel, et al.Pediatric Nephrology (Berlin, Germany)|December 11, 2008
Familial forms of nephrotic syndromeGianluca Caridi, Antonella Trivelli, Simone Sanna-Cherchi, et al.JCI Insight|December 9, 2025
Urobiota analysis and genome-wide association study in pediatric recurrent urinary tract infections and vesicoureteral refluxMiguel Verbitsky, Pavan Khosla, Daniel Bivona, et al.Journal of the American Society of Nephrology : JASN|December 11, 2021
GWAS in Mice Maps Susceptibility to HIV-Associated Nephropathy to the Ssbp2 LocusNicholas J Steers, Yask Gupta, Vivette D D'Agati, et al.Human Mutation|December 16, 2017
A noncoding variant in GANAB explains isolated polycystic liver disease (PCLD) in a large familyWhitney Besse, Jungmin Choi, Dina Ahram, et al.Pageof 12