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UK Renal Registry 15th annual report: Chapter 7 clinical, haematological and biochemical parameters in patients receiving renal replacement therapy in paediatric centres in the UK in 2011: national and centre-specific analyses.
Pruthi R, Maxwell H, Casula A, Braddon F, Lewis M, O'Brien C, Tse Y, Inward C, Sinha MD. Pruthi R, et al. Nephron Clin Pract. 2013;123 Suppl 1:151-64. doi: 10.1159/000353326. Epub 2013 Jun 10. Nephron Clin Pract. 2013. PMID: 23774490 Free article.
The HNF4A R76W mutation causes atypical dominant Fanconi syndrome in addition to a β cell phenotype.
Hamilton AJ, Bingham C, McDonald TJ, Cook PR, Caswell RC, Weedon MN, Oram RA, Shields BM, Shepherd M, Inward CD, Hamilton-Shield JP, Kohlhase J, Ellard S, Hattersley AT. Hamilton AJ, et al. Among authors: inward cd. J Med Genet. 2014 Mar;51(3):165-9. doi: 10.1136/jmedgenet-2013-102066. Epub 2013 Nov 27. J Med Genet. 2014. PMID: 24285859 Free PMC article.
UK Renal Registry 16th annual report: chapter 13 clinical, haematological and biochemical parameters in patients receiving renal replacement therapy in paediatric centres in the uk in 2012: national and centre-specific analyses.
Pruthi R, Maxwell H, Casula A, Braddon F, Lewis M, O'Brien C, Stojanovic J, Tse Y, Inward C, Sinha MD. Pruthi R, et al. Nephron Clin Pract. 2013;125(1-4):259-73. doi: 10.1159/000360032. Epub 2014 Feb 14. Nephron Clin Pract. 2013. PMID: 24662177 Free article.
UK Renal Registry 17th Annual Report: Chapter 9 Clinical, Haematological and Biochemical Parameters in Patients Receiving Renal Replacement Therapy in Paediatric Centres in the UK in 2013: National and Centre-specific Analyses.
Hamilton AJ, Pruthi R, Maxwell H, Casula A, Braddon F, Inward C, Lewis M, O'Brien C, Stojanovic J, Tse Y, Sinha MD. Hamilton AJ, et al. Nephron. 2015;129 Suppl 1:209-22. doi: 10.1159/000370279. Epub 2015 Jan 22. Nephron. 2015. PMID: 25695813 Free article.
61 results