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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1994 1
1996 2
1997 2
1998 2
1999 2
2000 1
2001 3
2002 3
2003 2
2004 1
2006 1
2007 3
2008 3
2009 1
2010 2
2011 1
2014 1
2016 1
2017 1
2020 1
2023 1
2024 0

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32 results

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Page 1
Randomized, Controlled Trial of Tacrolimus and Prednisolone Monotherapy for Adults with De Novo Minimal Change Disease: A Multicenter, Randomized, Controlled Trial.
Medjeral-Thomas NR, Lawrence C, Condon M, Sood B, Warwicker P, Brown H, Pattison J, Bhandari S, Barratt J, Turner N, Cook HT, Levy JB, Lightstone L, Pusey C, Galliford J, Cairns TD, Griffith M. Medjeral-Thomas NR, et al. Among authors: warwicker p. Clin J Am Soc Nephrol. 2020 Feb 7;15(2):209-218. doi: 10.2215/CJN.06180519. Epub 2020 Jan 17. Clin J Am Soc Nephrol. 2020. PMID: 31953303 Free PMC article. Clinical Trial.
Factor H--US?
Warwicker P, Goodship JA, Goodship TH. Warwicker P, et al. Nephrol Dial Transplant. 1998 Aug;13(8):1921-3. doi: 10.1093/ndt/13.8.1921. Nephrol Dial Transplant. 1998. PMID: 9719138 Review. No abstract available.
Factors determining penetrance in familial atypical haemolytic uraemic syndrome.
Sansbury FH, Cordell HJ, Bingham C, Bromilow G, Nicholls A, Powell R, Shields B, Smyth L, Warwicker P, Strain L, Wilson V, Goodship JA, Goodship TH, Turnpenny PD. Sansbury FH, et al. Among authors: warwicker p. J Med Genet. 2014 Nov;51(11):756-64. doi: 10.1136/jmedgenet-2014-102498. Epub 2014 Sep 26. J Med Genet. 2014. PMID: 25261570
Familial membranous nephropathy: an X-linked genetic susceptibility?
Bockenhauer D, Debiec H, Sebire N, Barratt M, Warwicker P, Ronco P, Kleta R. Bockenhauer D, et al. Among authors: warwicker p. Nephron Clin Pract. 2008;108(1):c10-5. doi: 10.1159/000112466. Epub 2007 Dec 13. Nephron Clin Pract. 2008. PMID: 18075275
Spinal cord infarction following central-line insertion.
Williams A, Little M, Gibbs J, Warwicker P, Farrington K. Williams A, et al. Among authors: warwicker p. Ren Fail. 2003 Mar;25(2):327-9. doi: 10.1081/jdi-120018735. Ren Fail. 2003. PMID: 12739841
Atypical haemolytic uraemic syndrome associated with a hybrid complement gene.
Venables JP, Strain L, Routledge D, Bourn D, Powell HM, Warwicker P, Diaz-Torres ML, Sampson A, Mead P, Webb M, Pirson Y, Jackson MS, Hughes A, Wood KM, Goodship JA, Goodship TH. Venables JP, et al. Among authors: warwicker p. PLoS Med. 2006 Oct;3(10):e431. doi: 10.1371/journal.pmed.0030431. PLoS Med. 2006. PMID: 17076561 Free PMC article.
32 results