James W. Ironside

Research interests

Publications

• Alpha‐synuclein RT ‐Qu IC in the CSF of patients with alpha‐synucleinopathies

  Annals of Clinical and Translational Neurology · 2016 · 10.1002/acn3.338

• Vascular cognitive impairment neuropathology guidelines (VCING): the contribution of cerebrovascular pathology to cognitive impairment

  Brain · 2016 · 10.1093/brain/aww214

• Aging-related tau astrogliopathy (ARTAG): harmonized evaluation strategy

  Acta Neuropathologica · 2015 · https://doi.org/10.1007/s00401-015-1509-x

• Florbetaben PET imaging to detect amyloid beta plaques in Alzheimer's disease: Phase 3 study

  Alzheimer s & Dementia · 2015 · 10.1016/j.jalz.2015.02.004

• Prevalent abnormal prion protein in human appendixes after bovine spongiform encephalopathy epizootic: large scale survey

  BMJ · 2013 · 10.1136/bmj.f5675

• Staging/typing of Lewy body related α-synuclein pathology: a study of the BrainNet Europe Consortium

  Acta Neuropathologica · 2009 · 10.1007/s00401-009-0523-2

• Predicting susceptibility and incubation time of human-to-human transmission of vCJD

  The Lancet Neurology · 2006 · 10.1016/s1474-4422(06)70413-6

• Preclinical variant CJD after blood transfusion in a PRNP codon 129 heterozygous patient

  · 2004

• Prevalence of lymphoreticular prion protein accumulation in UK tissue samples

  The Journal of Pathology · 2004 · 10.1002/path.1580

• Molecular classification of sporadic Creutzfeldt–Jakob disease

  Brain · 2003 · 10.1093/brain/awg125

• Results of a Randomized Study of Preradiation Chemotherapy Versus Radiotherapy Alone for Nonmetastatic Medulloblastoma: The International Society of Paediatric Oncology/United Kingdom Children’s Cancer Study Group PNET-3 Study

  Journal of Clinical Oncology · 2003 · 10.1200/jco.2003.05.116

• Diagnosing variant Creutzfeldt-Jakob disease with the pulvinar sign: MR imaging findings in 86 neuropathologically confirmed cases.

  PubMed · 2003

• The pulvinar sign on magnetic resonance imaging in variant Creutzfeldt-Jakob disease

  The Lancet · 2000 · 10.1016/s0140-6736(00)02140-1

• Diagnosis of new variant Creutzfeldt-Jakob disease

  Annals of Neurology · 2000 · 10.1002/1531-8249(200005)47:5<575::aid-ana4>3.0.co;2-w

• Genetic influence on the structural variations of the abnormal prion protein

  Proceedings of the National Academy of Sciences · 2000 · 10.1073/pnas.97.18.10168

• Investigation of variant Creutzfeldt-Jakob disease and other human prion diseases with tonsil biopsy samples

  The Lancet · 1999 · 10.1016/s0140-6736(98)12075-5

• Compelling transgenetic evidence for transmission of bovine spongiform encephalopathy prions to humans

  Proceedings of the National Academy of Sciences · 1999 · 10.1073/pnas.96.26.15137

• Prion immunoreactivity in appendix before clinical onset of variant Creutzfeldt-Jakob disease

  The Lancet · 1998 · 10.1016/s0140-6736(98)24035-9

• Transmissions to mice indicate that ‘new variant’ CJD is caused by the BSE agent

  Nature · 1997 · https://doi.org/10.1038/39057

• Diagnosis of new variant Creutzfeldt-Jakob disease by tonsil biopsy

  The Lancet · 1997 · 10.1016/s0140-6736(97)24002-x

• Diagnostic Criteria for Sporadic Creutzfeldt-Jakob Disease

  Archives of Neurology · 1996 · 10.1001/archneur.1996.00550090125018

• A new variant of Creutzfeldt-Jakob disease in the UK

  The Lancet · 1996 · https://doi.org/10.1016/s0140-6736(96)91412-9

• Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD

  Nature · 1996 · https://doi.org/10.1038/383685a0

• BSE transmission to macaques

  Nature · 1996 · 10.1038/381743a0

• Neuropathological Diagnostic Criteria for Creutzfeldt‐Jakob Disease (CJD) and Other Human Spongiform Encephalopathies (Prion Diseases)

  Brain Pathology · 1995 · 10.1111/j.1750-3639.1995.tb00625.x

Current projects

No projects listed.