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BMC Nephrology|May 2, 2019
Clinical practice guideline monitoring children and young people with, or at risk of developing autosomal dominant polycystic kidney disease (ADPKD)Jan Dudley, Paul Winyard, Matko Marlais, et al.The EMBO Journal|February 5, 2005
Trafficking of TRPP2 by PACS proteins represents a novel mechanism of ion channel regulationMichael Köttgen, Thomas Benzing, Thomas Simmen, et al.American Journal of Human Genetics|April 28, 2006
Quantification of homozygosity in consanguineous individuals with autosomal recessive diseaseC Geoffrey Woods, James Cox, Kelly Springell, et al.Kidney International|June 8, 2020
Novel nephronophthisis-associated variants reveal functional importance of MAPKBP1 dimerization for centriolar recruitmentRia Schönauer, Wenjun Jin, Anastasia Ertel, et al.Ebiomedicine|May 13, 2026
Prospective use of genomics in the evaluation of sudden cardiac death: results from a national health service population pathwayCian Wade, Richard Sandford, Frances Elmslie, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 29, 2014
Building a network of ADPKD reference centres across Europe: the EuroCYST initiativeKatja Petzold, Ron T Gansevoort, Albert C M Ong, et al.Nature Genetics|February 26, 2008
Mutations in the cyclin family member FAM58A cause an X-linked dominant disorder characterized by syndactyly, telecanthus and anogenital and renal malformationsSheila Unger, Detlef Böhm, Frank J Kaiser, et al.Ebiomedicine|May 24, 2022
The relationship between disease activity and UDCA response criteria in primary biliary cholangitis: A cohort studyDavid E J Jones, Aaron Wetten, Ben Barron-Millar, et al.Gut Microbes|May 16, 2023
Bacterial and metabolic phenotypes associated with inadequate response to ursodeoxycholic acid treatment in primary biliary cholangitisLaura Martinez-Gili, Alexandros Pechlivanis, Julie A K McDonald, et al.Hepatology (Baltimore, Md.)|June 15, 2021
The Serum Proteome and Ursodeoxycholic Acid Response in Primary Biliary CholangitisBen Barron-Millar, Laura Ogle, George Mells, et al.Pageof 4