Showing results (11-20 of 23) with videos related to
Sort By:
Pageof 3
American Journal of Human Genetics|January 6, 2015
Defects of CRB2 cause steroid-resistant nephrotic syndromeLwaki Ebarasi, Shazia Ashraf, Agnieszka Bierzynska, et al.American Journal of Human Genetics|May 13, 2014
Mutations in EMP2 cause childhood-onset nephrotic syndromeHeon Yung Gee, Shazia Ashraf, Xiaoyang Wan, et al.Human Mutation|July 1, 2015
WDR73 Mutations Cause Infantile Neurodegeneration and Variable Glomerular Kidney DiseaseJulia Vodopiutz, Rainer Seidl, Daniela Prayer, et al.The Journal of Clinical Investigation|May 12, 2015
KANK deficiency leads to podocyte dysfunction and nephrotic syndromeHeon Yung Gee, Fujian Zhang, Shazia Ashraf, et al.Kidney International|September 2, 2019
Mutations in KIRREL1, a slit diaphragm component, cause steroid-resistant nephrotic syndromeAshish K Solanki, Eugen Widmeier, Ehtesham Arif, 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.Nature Genetics|February 16, 2016
Mutations in nuclear pore genes NUP93, NUP205 and XPO5 cause steroid-resistant nephrotic syndromeDaniela A Braun, Carolin E Sadowski, Stefan Kohl, et al.Brain : a Journal of Neurology|June 14, 2015
Recessive nephrocerebellar syndrome on the Galloway-Mowat syndrome spectrum is caused by homozygous protein-truncating mutations of WDR73Robert N Jinks, Erik G Puffenberger, Emma Baple, et al.Nature Communications|February 25, 2016
FAT1 mutations cause a glomerulotubular nephropathyHeon Yung Gee, Carolin E Sadowski, Pardeep K Aggarwal, et al.Clinical Journal of the American Society of Nephrology : CJASN|November 12, 2017
Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic SyndromeJillian K Warejko, Weizhen Tan, Ankana Daga, et al.Pageof 3