Ironside JW - Search Results

1

Prion infectivity in the spleen of a PRNP heterozygous individual with subclinical variant Creutzfeldt-Jakob disease.

Bishop MT, Diack AB, Ritchie DL, Ironside JW, Will RG, Manson JC. Bishop MT, et al. Among authors: ironside jw. Brain. 2013 Apr;136(Pt 4):1139-45. doi: 10.1093/brain/awt032. Epub 2013 Feb 28. Brain. 2013. PMID: 23449776 Free PMC article.

2

Clinical, neuropathological and immunohistochemical features of sporadic and variant forms of Creutzfeldt-Jakob disease in the squirrel monkey (Saimiri sciureus).

Williams L, Brown P, Ironside J, Gibson S, Will R, Ritchie D, Kreil TR, Abee C. Williams L, et al. J Gen Virol. 2007 Feb;88(Pt 2):688-695. doi: 10.1099/vir.0.81957-0. J Gen Virol. 2007. PMID: 17251588

3

Prion protein heterogeneity in sporadic but not variant Creutzfeldt-Jakob disease: UK cases 1991-2002.

Head MW, Bunn TJ, Bishop MT, McLoughlin V, Lowrie S, McKimmie CS, Williams MC, McCardle L, MacKenzie J, Knight R, Will RG, Ironside JW. Head MW, et al. Among authors: ironside jw. Ann Neurol. 2004 Jun;55(6):851-9. doi: 10.1002/ana.20127. Ann Neurol. 2004. PMID: 15174020

4

Preclinical vCJD after blood transfusion in a PRNP codon 129 heterozygous patient.

Peden AH, Head MW, Ritchie DL, Bell JE, Ironside JW. Peden AH, et al. Among authors: ironside jw. Lancet. 2004 Aug 7-13;364(9433):527-9. doi: 10.1016/S0140-6736(04)16811-6. Lancet. 2004. PMID: 15302196

5

Detection of type 1 prion protein in variant Creutzfeldt-Jakob disease.

Yull HM, Ritchie DL, Langeveld JP, van Zijderveld FG, Bruce ME, Ironside JW, Head MW. Yull HM, et al. Among authors: ironside jw. Am J Pathol. 2006 Jan;168(1):151-7. doi: 10.2353/ajpath.2006.050766. Am J Pathol. 2006. PMID: 16400018 Free PMC article.

6

Risks of transmission of variant Creutzfeldt-Jakob disease by blood transfusion.

Peden AH, Ritchie DL, Ironside JW. Peden AH, et al. Among authors: ironside jw. Folia Neuropathol. 2005;43(4):271-8. Folia Neuropathol. 2005. PMID: 16416391 Free article. Review.

7

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. Among authors: ironside jw. Am J Pathol. 2006 Mar;168(3):927-35. doi: 10.2353/ajpath.2006.050788. Am J Pathol. 2006. PMID: 16507908 Free PMC article.

8

Variant Creutzfeldt-Jakob disease: prion protein genotype analysis of positive appendix tissue samples from a retrospective prevalence study.

Ironside JW, Bishop MT, Connolly K, Hegazy D, Lowrie S, Le Grice M, Ritchie DL, McCardle LM, Hilton DA. Ironside JW, et al. BMJ. 2006 May 20;332(7551):1186-8. doi: 10.1136/bmj.38804.511644.55. Epub 2006 Apr 10. BMJ. 2006. PMID: 16606639 Free PMC article.

9

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. Among authors: ironside jw. J Gen Virol. 2006 Oct;87(Pt 10):3119-3124. doi: 10.1099/vir.0.81935-0. J Gen Virol. 2006. PMID: 16963772

10

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. Among authors: ironside jw. J Gen Virol. 2007 Mar;88(Pt 3):1068-1072. doi: 10.1099/vir.0.81913-0. J Gen Virol. 2007. PMID: 17325383

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