A case of acute tubulointerstitial nephritis following administration of the Oxford-AstraZeneca COVID-19 vaccine: a case report von Williams, Samuel B M, Holwill, Stephen D J, Clissold, Rhian L, Bingham, Coralie

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Genome-wide methylomic analysis in individuals with HNF1B intragenic mutation and 17q12 microdeletion von Clissold, Rhian L, Ashfield, Beth, Burrage, Joe, Hannon, Eilis, Bingham, Coralie, Mill, Jonathan, Hattersley, Andrew, Dempster, Emma L

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Discovery of a novel dominant mutation in the REN gene after forty years of renal disease: a case report von Clissold, Rhian L, Clarke, Helen C, Spasic-Boskovic, Olivera, Brugger, Kim, Abbs, Stephen, Bingham, Coralie, Shaw-Smith, Charles

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

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Sociodemographic, Psychologic Health, and Lifestyle Outcomes in Young Adults on Renal Replacement Therapy von Hamilton, Alexander J, Clissold, Rhian L, Inward, Carol D, Caskey, Fergus J, Ben-Shlomo, Yoav

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Young adults’ perspectives on living with kidney failure: a systematic review and thematic synthesis of qualitative studies von Bailey, Phillippa K, Hamilton, Alexander J, Clissold, Rhian L, Inward, Carol D, Caskey, Fergus J, Ben-Shlomo, Yoav, Owen-Smith, Amanda

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Familial interstitial nephritis: 42 years from case series to genetic diagnosis von Clissold, Rhian L, Bingham, Coralie, Shaw-Smith, Charles

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Comment on Dubois-Laforgue et al. Diabetes, Associated Clinical Spectrum, Long-term Prognosis, and Genotype/Phenotype Correlations in 201 Adult Patients With Hepatocyte Nuclear Fac... von Clissold, Rhian L, Harries, Lorna W, Ellard, Sian, Bingham, Coralie, Hattersley, Andrew T

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Diabetes, Associated Clinical Spectrum, Long-term Prognosis, and Genotype/ Phenotype Correlations in 201 Adult Patients With Hepatocyte Nuclear Factor 1B (HNF1B) Molecular Defects.... von Clissold, Rhian L, Harries, Lorna W, Ellard, Sian, Bingham, Coralie, Hattersley, Andrew T

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Exocrine pancreatic dysfunction is common in hepatocyte nuclear factor 1β-associated renal disease and can be symptomatic von Clissold, Rhian L, Fulford, Jon, Hudson, Michelle, Shields, Beverley M, McDonald, Timothy J, Ellard, Sian, Hattersley, Andrew T, Bingham, Coralie

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SP030HNF1B WHOLE-GENE DELETIONS ARE ASSOCIATED WITH AUTISTIC TRAITS von Clissold, Rhian L, Ellard, Sian, Hattersley, Andrew T, Bingham, Coralie

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Exocrine pancreatic dysfunction is common in hepatocyte nuclear factor 1[beta]-associated renal disease and can be symptomatic von Clissold, Rhian L, Fulford, Jon, Hudson, Michelle, Shields, Beverley M, Mcdonald, Timothy J, Ellard, Sian, Hattersley, Andrew T, Bingham, Coralie

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