Neuropathology of variant Creutzfeldt-Jakob diseaseIRONSIDE, James W.Comptes rendus. Biologies. 2002, Vol 325, Num 1, pp 27-31, issn 1631-0691Article

De l'ESB à Creutzfeldt-Jakob = From BSE to Creutzfeld-JakobIRONSIDE, James W.Biofutur (Puteaux). 2001, pp 6-10, issn 0294-3506, HSArticle

The brain smear, a rapid affordable intraoperative diagnostic technique for brain tumours appropriate for AfricaOLASODE, Babatunde J; IRONSIDE, James W.Tropical doctor. 2004, Vol 34, Num 4, pp 223-225, issn 0049-4755, 3 p.Article

The spectrum of safety: Variant Creutzfeldt-Jakob disease in the United KingdomIRONSIDE, James W.Seminars in hematology. 2003, Vol 40, Num 3, pp 16-22, issn 0037-1963, 7 p., SUP3Article

A young man with rapidly progressive multifocal disease affecting the white matterHILTON-JONES, David; IRONSIDE, James W; SIMPSON, David J et al.Practical neurology (Print). 2007, Vol 7, Num 3, pp 172-181, issn 1474-7758, 10 p.Article

Disease-associated prion protein in vessel wallsKOPEREK, Oskar; KOVACS, Gabor G; RITCHIE, Diane et al.The American journal of pathology. 2002, Vol 161, Num 6, pp 1979-1984, issn 0002-9440, 6 p.Article

Comparison of the level, distribution and form of disease-associated prion protein in variant and sporadic Creutzfeldt-Jakob diseased brain using conformation-dependent immunoassay and Western blotYOUNG PYO CHOI; GRÖNER, Albrecht; IRONSIDE, James W et al.Journal of general virology. 2011, Vol 92, pp 727-732, issn 0022-1317, 6 p., 3Article

Sensitive and specific detection of sporadic Creutzfeldt―Jakob disease brain prion protein using real-time quaking-induced conversionPEDEN, Alexander H; MCGUIRE, Lynne I; GREEN, Alison J. E et al.Journal of general virology. 2012, Vol 93, pp 438-449, issn 0022-1317, 12 p., 2Article

Biological Effects and Use of PrP^Sc- and PrP-Specific Antibodies Generated by Immunization with Purified Full-Length Native Mouse PrionsPETSCH, Benjamin; MÜLLER-SCHIFFMANN, Andreas; LEHLE, Anna et al.Journal of virology. 2011, Vol 85, Num 9, pp 4538-4546, issn 0022-538X, 9 p.Article

Peripheral tissue involvement in sporadic, latrogenic, and variant Creutzfeldt-Jakob disease: An immunohistochemical, quantitative, and biochemical studyHEAD, Mark W; RITCHIE, Diane; SMITH, Nadine et al.The American journal of pathology. 2004, Vol 164, Num 1, pp 143-153, issn 0002-9440, 11 p.Article

Diagnosing variant Creutzfeldt-Jakob disease with the pulvinar sign: MR imaging findings in 86 neuropathologically confirmed casesCOLLIE, Donald A; SUMMERS, David M; SELLAR, Robin J et al.American journal of neuroradiology. 2003, Vol 24, Num 8, pp 1560-1569, issn 0195-6108, 10 p.Article

Validation of Diagnostic Criteria for Variant Creutzfeldt-Jakob DiseaseHEATH, Craig A; COOPER, Sarah A; SUMMERS, David M et al.Annals of neurology. 2010, Vol 67, Num 6, pp 761-770, issn 0364-5134, 10 p.Article

Mutations of the Prion Protein Gene: Phenotypic SpectrumKOVACS, Gabor G; TRABATTONI, Gianriccardo; HAINFELLNER, Johannes A et al.Journal of neurology. 2002, Vol 249, Num 11, pp 1567-1582, issn 0340-5354, 16 p.Article

Accumulation of prion protein in tonsil and appendix : Review of tissue samplesHILTON, David A; GHANI, Azra C; CONYERS, Lisa et al.BMJ. British medical journal (International ed.). 2002, Vol 325, Num 7365, pp 633-634, issn 0959-8146Article

Gerstmann-Straüssler-Scheinker disease: Novel PRNP mutation and VGKC-complex antibodiesJONES, Matthew; ODUNSI, Sola; DU PLESSIS, Daniel et al.Neurology. 2014, Vol 82, Num 23, pp 2107-2111, issn 0028-3878, 5 p.Article

Variably protease-sensitive prionopathy in the UK: a retrospective review 1991―2008HEAD, Mark W; YULL, Helen M; RITCHIE, Diane L et al.Brain. 2013, Vol 136, pp 1102-1115, issn 0006-8950, 14 p., 4Article

Human embryonic stem cells rapidly take up and then clear exogenous human and animal prions in vitroKREJCIOVA, Zuzana; PELLS, Steve; DE SOUSA, Paul et al.Journal of pathology (Print). 2011, Vol 223, Num 5, pp 635-645, issn 0022-3417, 11 p.Article

Inherited prion disease with 4-octapeptide repeat insertion: disease requires the interaction of multiple genetic risk factorsKASKI, Diego N; PENNINGTON, Catherine; KNIGHT, Richard S. G et al.Brain. 2011, Vol 134, pp 1829-1838, issn 0006-8950, 10 p., 6Article

Effects of human PrP^Sc type and PRNP genotype in an in-vitro conversion assayJONES, Michael; PEDEN, Alexander H; WIGHT, Darren et al.Neuroreport (Oxford). 2008, Vol 19, Num 18, pp 1783-1786, issn 0959-4965, 4 p.Article

Detection of type 1 prion protein in variant Creutzfeldt-Jakob diseaseYULL, Helen M; RITCHIE, Diane L; LANGEVELD, Jan P. M et al.The American journal of pathology. 2006, Vol 168, Num 1, pp 151-157, issn 0002-9440, 7 p.Article

Molecular classification of sporadic Creutzfeldt-Jakob diseaseHILL, Andrew F; JOINER, Susan; WADSWORTH, Jonathan D. F et al.Brain. 2003, Vol 126, pp 1333-1346, issn 0006-8950, 14 p., 6Article

Abnormal prion protein in the pituitary in sporadic and variant Creutzfeldt-Jakob diseasePEDEN, Alexander H; RITCHIE, Diane L; UDDIN, Hafsana P et al.Journal of general virology. 2007, Vol 88, pp 1068-1072, issn 0022-1317, 5 p., 3Article

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 diseaseLOURENCO, Paula C; SCHMERR, Mary Jo; MACGREGOR, Ian et al.Journal of general virology. 2006, Vol 87, pp 3119-3124, issn 0022-1317, 6 p., 10Article

Determinants of diagnostic investigation sensitivities across the clinical spectrum of sporadic Creutzfeldt-Jakob diseaseHEAD, Mark W; IRONSIDE, James W; CUADRADO-CORRALES, N et al.Brain. 2006, Vol 129, issn 0006-8950, 2238-2240,2278-2287 [13 p.], 9Article

Preclinical vCJD after blood transfusion in a PRNP codon 129 heterozygous patientPEDEN, Alexander H; HEAD, Mark W; RITCHIE, Diane L et al.Lancet (British edition). 2004, Vol 364, Num 9433, pp 527-529, issn 0140-6736, 3 p.Article