Showing results (61-70 of 69) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 69 results.
Human Molecular Genetics|December 18, 2024
Use of patient-derived cell models for characterization of compound heterozygous hypomorphic C2CD3 variants in a patient with isolated nephronophthisisZachary T Sentell, Lina Mougharbel, Zachary W Nurcombe, et al.
Canadian Journal of Kidney Health and Disease|May 12, 2015
The Canadian Childhood Nephrotic Syndrome (CHILDNEPH) Project: overview of design and methodsSusan Samuel, Shannon Scott, Catherine Morgan, et al.
Genome Medicine|May 23, 2022
Rapid whole genome sequencing of critically ill pediatric patients from genetically underrepresented populationsNour Halabi, Sathishkumar Ramaswamy, Maha El Naofal, et al.
Pediatric Nephrology (Berlin, Germany)|April 11, 2015
An international consensus approach to the management of atypical hemolytic uremic syndrome in childrenChantal Loirat, Fadi Fakhouri, Gema Ariceta, et al.
Kidney International Reports|October 27, 2025
Efficacy of Calcineurin Inhibition in Children With Steroid-Resistant Nephrotic SyndromeAgnes Trautmann, Jonas Hofstetter, Beata Lipska-Ziętkiewicz, et al.
The Journal of Pediatrics|January 8, 2021
Predicting Adverse Outcomes for Shiga Toxin-Producing Escherichia coli Infections in Emergency DepartmentsChu Yang Lin, Jianling Xie, Stephen B Freedman, et al.
Genome Medicine|January 26, 2023
The genomic landscape of rare disorders in the Middle EastMaha El Naofal, Sathishkumar Ramaswamy, Ali Alsarhan, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|May 25, 2019
Predicting Hemolytic Uremic Syndrome and Renal Replacement Therapy in Shiga Toxin-producing Escherichia coli-infected ChildrenRyan S McKee, David Schnadower, Phillip I Tarr, et al.
Human Mutation|November 19, 2011
Spectrum of mutations in the renin-angiotensin system genes in autosomal recessive renal tubular dysgenesisOlivier Gribouval, Vincent Morinière, Audrey Pawtowski, et al.
Pageof 7