Ironside J - Search Results

1

Variation in concentration of prion protein in the peripheral blood of patients with variant and sporadic Creutzfeldt-Jakob disease detected by dissociation enhanced lanthanide fluoroimmunoassay and flow cytometry.

Fagge T, Barclay GR, Macgregor I, Head M, Ironside J, Turner M. Fagge T, et al. Among authors: ironside j. Transfusion. 2005 Apr;45(4):504-13. doi: 10.1111/j.0041-1132.2005.04342.x. Transfusion. 2005. PMID: 15819670 Clinical Trial.

2

Neuropathology of variant Creutzfeldt-Jakob disease.

Ironside JW, Head MW, McCardle L, Knight R. Ironside JW, et al. Acta Neurobiol Exp (Wars). 2002;62(3):175-82. doi: 10.55782/ane-2002-1436. Acta Neurobiol Exp (Wars). 2002. PMID: 12416395 Free article.

3

Detection and localization of PrPSc in the skeletal muscle of patients with variant, iatrogenic, and sporadic forms of Creutzfeldt-Jakob disease.

Peden AH, Ritchie DL, Head MW, Ironside JW. Peden AH, et al. Am J Pathol. 2006 Mar;168(3):927-35. doi: 10.2353/ajpath.2006.050788. Am J Pathol. 2006. PMID: 16507908 Free PMC article.

4

Sporadic Creutzfeldt-Jakob disease: further twists and turns in a convoluted protein.

Head MW, Ironside JW. Head MW, et al. Brain. 2006 Sep;129(Pt 9):2238-40. doi: 10.1093/brain/awl225. Brain. 2006. PMID: 16923953 No abstract available.

5

Application of an immunocapillary electrophoresis assay to the detection of abnormal prion protein in brain, spleen and blood specimens from patients with variant Creutzfeldt-Jakob disease.

Lourenco PC, Schmerr MJ, MacGregor I, Will RG, Ironside JW, Head MW. Lourenco PC, et al. J Gen Virol. 2006 Oct;87(Pt 10):3119-3124. doi: 10.1099/vir.0.81935-0. J Gen Virol. 2006. PMID: 16963772

6

Abnormal prion protein in the pituitary in sporadic and variant Creutzfeldt-Jakob disease.

Peden AH, Ritchie DL, Uddin HP, Dean AF, Schiller KAF, Head MW, Ironside JW. Peden AH, et al. J Gen Virol. 2007 Mar;88(Pt 3):1068-1072. doi: 10.1099/vir.0.81913-0. J Gen Virol. 2007. PMID: 17325383

7

Application of Atomic Dielectric Resonance Spectroscopy for the screening of blood samples from patients with clinical variant and sporadic CJD.

Fagge TJ, Barclay GR, Stove GC, Stove G, Robinson MJ, Head MW, Ironside JW, Turner ML. Fagge TJ, et al. Among authors: ironside jw. J Transl Med. 2007 Aug 30;5:41. doi: 10.1186/1479-5876-5-41. J Transl Med. 2007. PMID: 17760958 Free PMC article.

8

Human platelets as a substrate source for the in vitro amplification of the abnormal prion protein (PrP) associated with variant Creutzfeldt-Jakob disease.

Jones M, Peden AH, Yull H, Wight D, Bishop MT, Prowse CV, Turner ML, Ironside JW, MacGregor IR, Head MW. Jones M, et al. Transfusion. 2009 Feb;49(2):376-84. doi: 10.1111/j.1537-2995.2008.01954.x. Epub 2008 Oct 29. Transfusion. 2009. PMID: 18980616

9

Further characterisation of the prion protein molecular types detectable in the NIBSC Creutzfeldt-Jakob disease brain reference materials.

Yull HM, Ironside JW, Head MW. Yull HM, et al. Biologicals. 2009 Aug;37(4):210-5. doi: 10.1016/j.biologicals.2009.01.009. Epub 2009 Mar 4. Biologicals. 2009. PMID: 19264507

10

Sporadic Creutzfeldt-Jakob disease: discrete subtypes or a spectrum of disease?

Head MW, Ironside JW. Head MW, et al. Brain. 2009 Oct;132(Pt 10):2627-9. doi: 10.1093/brain/awp225. Epub 2009 Sep 16. Brain. 2009. PMID: 19759201 No abstract available.

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