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Page 1
Identification of a mutation in complement factor H-related protein 5 in patients of Cypriot origin with glomerulonephritis.
Gale DP, de Jorge EG, Cook HT, Martinez-Barricarte R, Hadjisavvas A, McLean AG, Pusey CD, Pierides A, Kyriacou K, Athanasiou Y, Voskarides K, Deltas C, Palmer A, Frémeaux-Bacchi V, de Cordoba SR, Maxwell PH, Pickering MC. Gale DP, et al. Among authors: maxwell ph. Lancet. 2010 Sep 4;376(9743):794-801. doi: 10.1016/S0140-6736(10)60670-8. Epub 2010 Aug 25. Lancet. 2010. PMID: 20800271 Free PMC article.
C3 glomerulonephritis and CFHR5 nephropathy.
Gale DP, Maxwell PH. Gale DP, et al. Among authors: maxwell ph. Nephrol Dial Transplant. 2013 Feb;28(2):282-8. doi: 10.1093/ndt/gfs441. Epub 2012 Nov 2. Nephrol Dial Transplant. 2013. PMID: 23125424 Review.
A functional variant in NEPH3 gene confers high risk of renal failure in primary hematuric glomerulopathies. Evidence for predisposition to microalbuminuria in the general population.
Voskarides K, Stefanou C, Pieri M, Demosthenous P, Felekkis K, Arsali M, Athanasiou Y, Xydakis D, Stylianou K, Daphnis E, Goulielmos G, Loizou P, Savige J, Höhne M, Völker LA, Benzing T, Maxwell PH, Gale DP, Gorski M, Böger C, Kollerits B, Kronenberg F, Paulweber B, Zavros M, Pierides A, Deltas C. Voskarides K, et al. Among authors: maxwell ph. PLoS One. 2017 Mar 23;12(3):e0174274. doi: 10.1371/journal.pone.0174274. eCollection 2017. PLoS One. 2017. PMID: 28334007 Free PMC article.
The role of HIF in immunity.
Gale DP, Maxwell PH. Gale DP, et al. Among authors: maxwell ph. Int J Biochem Cell Biol. 2010 Apr;42(4):486-94. doi: 10.1016/j.biocel.2009.10.012. Epub 2009 Oct 17. Int J Biochem Cell Biol. 2010. PMID: 19840863 Review.
Familial C3 glomerulopathy associated with CFHR5 mutations: clinical characteristics of 91 patients in 16 pedigrees.
Athanasiou Y, Voskarides K, Gale DP, Damianou L, Patsias C, Zavros M, Maxwell PH, Cook HT, Demosthenous P, Hadjisavvas A, Kyriacou K, Zouvani I, Pierides A, Deltas C. Athanasiou Y, et al. Among authors: maxwell ph. Clin J Am Soc Nephrol. 2011 Jun;6(6):1436-46. doi: 10.2215/CJN.09541010. Epub 2011 May 12. Clin J Am Soc Nephrol. 2011. PMID: 21566112 Free PMC article.
End-stage renal failure associated with congenital deafness.
Annear NM, Gale DP, Loughlin S, Dorkins HR, Maxwell PH. Annear NM, et al. Among authors: maxwell ph. NDT Plus. 2008 Jun;1(3):171-5. doi: 10.1093/ndtplus/sfn019. Epub 2008 Mar 27. NDT Plus. 2008. PMID: 25983868 Free PMC article. No abstract available.
Mutations in mitochondrial DNA causing tubulointerstitial kidney disease.
Connor TM, Hoer S, Mallett A, Gale DP, Gomez-Duran A, Posse V, Antrobus R, Moreno P, Sciacovelli M, Frezza C, Duff J, Sheerin NS, Sayer JA, Ashcroft M, Wiesener MS, Hudson G, Gustafsson CM, Chinnery PF, Maxwell PH. Connor TM, et al. Among authors: maxwell ph. PLoS Genet. 2017 Mar 7;13(3):e1006620. doi: 10.1371/journal.pgen.1006620. eCollection 2017 Mar. PLoS Genet. 2017. PMID: 28267784 Free PMC article.
326 results