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Clinical Kidney Journal|June 28, 2013
Focal segmental glomerulosclerosis in association with neurofibromatosis type 1: a case report and proposed molecular pathwaysFarsad Afshinnia, Virginia Vega-Warner, Paul KillenKidney International|March 23, 2005
Differential proteomic analysis of proteins induced by glucocorticoids in cultured murine podocytesRichard F Ransom, Virginia Vega-Warner, William E Smoyer, et al.Pediatric Nephrology (Berlin, Germany)|October 31, 2009
Adequate use of allele frequencies in Hispanics--a problem elucidated in nephrotic syndromeGil Chernin, Saskia F Heeringa, Virginia Vega-Warner, et al.Kidney International|October 22, 2004
Induction of antioxidant enzymes in murine podocytes precedes injury by puromycin aminonucleosideVirginia Vega-Warner, Richard F Ransom, Andrea M Vincent, et al.Nephron. Clinical Practice|May 16, 2012
Mutation analysis of NPHS1 in a worldwide cohort of congenital nephrotic syndrome patientsBugsu Ovunc, Shazia Ashraf, Virginia Vega-Warner, et al.Annals of Saudi Medicine|January 14, 2014
Steroid-resistant nephrotic syndrome: impact of genetic testingJameela A Kari, Sherif M El-Desoky, Mamdooh Gari, et al.Plos One|June 25, 2015
Whole Exome Sequencing Reveals Novel PHEX Splice Site Mutations in Patients with Hypophosphatemic RicketsSara L Ma, Virginia Vega-Warner, Christopher Gillies, et al.Pediatric Nephrology (Berlin, Germany)|October 22, 2016
Evaluating Mendelian nephrotic syndrome genes for evidence for risk alleles or oligogenicity that explain heritabilityBrendan D Crawford, Christopher E Gillies, Catherine C Robertson, et al.Pediatric Nephrology (Berlin, Germany)|June 11, 2008
Low prevalence of NPHS2 mutations in African American children with steroid-resistant nephrotic syndromeGil Chernin, Saskia F Heeringa, Rasheed Gbadegesin, et al.Pediatric Nephrology (Berlin, Germany)|March 3, 2011
Respiratory-chain deficiency presenting as diffuse mesangial sclerosis with NPHS3 mutationEsra Baskin, Umut Selda Bayrakci, Füsun Alehan, et al.Pageof 5