A case of acute tubulointerstitial nephritis following administration of the Oxford-AstraZeneca COVID-19 vaccine: a case report

por Williams, Samuel B. M., Holwill, Stephen D. J., Clissold, Rhian L., Bingham, Coralie
Publicado 2023

Discovery of a novel dominant mutation in the REN gene after forty years of renal disease: a case report

por Clissold, Rhian L., Clarke, Helen C., Spasic-Boskovic, Olivera, Brugger, Kim, Abbs, Stephen, Bingham, Coralie, Shaw-Smith, Charles
Publicado 2017

Genome-wide methylomic analysis in individuals with HNF1B intragenic mutation and 17q12 microdeletion

por Clissold, Rhian L., Ashfield, Beth, Burrage, Joe, Hannon, Eilis, Bingham, Coralie, Mill, Jonathan, Hattersley, Andrew, Dempster, Emma L.
Publicado 2018

Exocrine pancreatic dysfunction is common in hepatocyte nuclear factor 1β-associated renal disease and can be symptomatic

por Clissold, Rhian L, Fulford, Jon, Hudson, Michelle, Shields, Beverley M, McDonald, Timothy J, Ellard, Sian, Hattersley, Andrew T, Bingham, Coralie
Publicado 2018

Young adults’ perspectives on living with kidney failure: a systematic review and thematic synthesis of qualitative studies

por Bailey, Phillippa K, Hamilton, Alexander J, Clissold, Rhian L, Inward, Carol D, Caskey, Fergus J, Ben-Shlomo, Yoav, Owen-Smith, Amanda
Publicado 2018

Chromosome 17q12 microdeletions but not intragenic HNF1B mutations link developmental kidney disease and psychiatric disorder

por Clissold, Rhian L., Shaw-Smith, Charles, Turnpenny, Peter, Bunce, Benjamin, Bockenhauer, Detlef, Kerecuk, Larissa, Waller, Simon, Bowman, Pamela, Ford, Tamsin, Ellard, Sian, Hattersley, Andrew T., Bingham, Coralie
Publicado 2016