Canlyniadau Chwilio - Inward, Carol D
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The clinical epidemiology of young adults starting renal replacement therapy in the UK: presentation, management and survival using 15 years of UK Renal Registry data gan Hamilton, Alexander J., Casula, Anna, Ben-Shlomo, Yoav, Caskey, Fergus J., Inward, Carol D.
Cyhoeddwyd 2017Text -
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The clinical epidemiology of young adults starting renal replacement therapy in the UK: presentation, management and survival using 15 years of UK Renal Registry data gan Hamilton, Alexander J, Casula, Anna, Ben-Shlomo, Yoav, Caskey, Fergus J, Inward, Carol D
Cyhoeddwyd 2018Text -
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The clinical epidemiology of young adults starting renal replacement therapy in the UK: presentation, management and survival using 15 years of UK Renal Registry data gan Hamilton, Alexander J., Casula, Anna, Ben-Shlomo, Yoav, Caskey, Fergus J., Inward, Carol D.
Cyhoeddwyd 2017Text -
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Associations between Deprivation, Geographic Location, and Access to Pediatric Kidney Care in the United Kingdom gan Plumb, Lucy A., Sinha, Manish D., Casula, Anna, Inward, Carol D., Marks, Stephen D., Caskey, Fergus J., Ben-Shlomo, Yoav
Cyhoeddwyd 2021Text -
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Young adults’ perspectives on living with kidney failure: a systematic review and thematic synthesis of qualitative studies gan Bailey, Phillippa K, Hamilton, Alexander J, Clissold, Rhian L, Inward, Carol D, Caskey, Fergus J, Ben-Shlomo, Yoav, Owen-Smith, Amanda
Cyhoeddwyd 2018Text -
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Initial Steroid Sensitivity in Children with Steroid-Resistant Nephrotic Syndrome Predicts Post-Transplant Recurrence gan Ding, Wen Y., Koziell, Ania, McCarthy, Hugh J., Bierzynska, Agnieszka, Bhagavatula, Murali K., Dudley, Jan A., Inward, Carol D., Coward, Richard J., Tizard, Jane, Reid, Christopher, Antignac, Corinne, Boyer, Olivia, Saleem, Moin A.
Cyhoeddwyd 2014Text -
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MAGI2 Mutations Cause Congenital Nephrotic Syndrome gan Bierzynska, Agnieszka, Soderquest, Katrina, Dean, Philip, Colby, Elizabeth, Rollason, Ruth, Jones, Caroline, Inward, Carol D., McCarthy, Hugh J., Simpson, Michael A., Lord, Graham M., Williams, Maggie, Welsh, Gavin I., Koziell, Ania B., Saleem, Moin A.
Cyhoeddwyd 2017Text -
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The HNF4A R76W mutation causes atypical dominant Fanconi syndrome in addition to a β cell phenotype gan 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
Cyhoeddwyd 2014Text