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Pediatric 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.Saudi Medical Journal|September 22, 2016
Prevalence of hypertension, obesity, hematuria and proteinuria amongst healthy adolescents living in Western Saudi ArabiaKholoud A Hothan, Bashaer A Alasmari, Omniya K Alkhelaiwi, et al.Pediatric Nephrology (Berlin, Germany)|December 25, 2012
Renal impairment in children with posterior urethral valvesJameela Abdulaziz Kari, Sherif El-Desoky, Youssef M K Farag, et al.American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 27, 2017
HLA-DQA1 and APOL1 as Risk Loci for Childhood-Onset Steroid-Sensitive and Steroid-Resistant Nephrotic SyndromeAdebowale Adeyemo, Christopher Esezobor, Adaobi Solarin, et al.JCI Insight|December 7, 2021
Steroid-sensitive nephrotic syndrome candidate gene CLVS1 regulates podocyte oxidative stress and endocytosisBrandon M Lane, Megan Chryst-Stangl, Guanghong Wu, et al.American Journal of Medical Genetics. Part A|June 19, 2021
Homozygous WNT9B variants in two families with bilateral renal agenesis/hypoplasia/dysplasiaGabrielle Lemire, Bixia Zheng, Grace U Ediae, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|October 24, 2020
Mutations in transcription factor CP2-like 1 may cause a novel syndrome with distal renal tubulopathy in humansVerena Klämbt, Max Werth, Ana C Onuchic-Whitford, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 2, 2020
Phenotype expansion of heterozygous FOXC1 pathogenic variants toward involvement of congenital anomalies of the kidneys and urinary tract (CAKUT)Chen-Han Wilfred Wu, Nina Mann, Makiko Nakayama, 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.Journal of the American Society of Nephrology : JASN|October 29, 2014
A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndromeCarolin E Sadowski, Svjetlana Lovric, Shazia Ashraf, et al.Pageof 4