Late presentation of toxoplasmosis in renal transplant recipients

by Clissold, Rhian, Bingham, Coralie
Published 2010

Assessment of the HNF1B Score as a Tool to Select Patients for HNF1B Genetic Testing

by Clissold, Rhian, Shields, Beverley, Ellard, Sian, Hattersley, Andrew, Bingham, Coralie
Published 2015

Prevalence in the General Population of a CFH Sequence Variant Associated with Atypical Haemolytic Uraemic Syndrome in an Extensive Family from Southwest England

by Hamilton, Alexander J., Lyons, Carl B.A., Goodship, Timothy H.J., Bingham, Coralie
Published 2013

RET gene mutations are not a common cause of congenital solitary functioning kidney in adults

by Oram, Richard A., Edghill, Emma L., Woolf, Adrian S., Hennekam, R. C., Ellard, Sian, Hattersley, A. T., Bingham, Coralie
Published 2009

Urine C-peptide creatinine ratio can be used to assess insulin resistance and insulin production in people without diabetes: an observational study

by Oram, Richard A, Rawlingson, Andrew, Shields, Beverley M, Bingham, Coralie, Besser, Rachel E J, McDonald, Tim J, Knight, Bridget A, Hattersley, Andrew T
Published 2013

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

by 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
Published 2016

The HNF4A R76W mutation causes atypical dominant Fanconi syndrome in addition to a β cell phenotype

by Hamilton, Alexander J, Bingham, Coralie, McDonald, Timothy J, Cook, Paul R, Caswell, Richard C, Weedon, Michael N, Oram, Richard A, Shields, Beverley M, Shepherd, Maggie, Inward, Carol D, Hamilton-Shield, Julian P, Kohlhase, Jürgen, Ellard, Sian, Hattersley, Andrew T
Published 2014