AB Tullo, RJ Buckley, T Kelly, MW Head, P … - Clinical &# 38; Experimental Ophthalmology, 2006 - ingentaconnect.com Eight years after the event, two patients remain free of symptoms suggestive of
iatrogenic CJD ( http://www.cjd.ed.ac.uk/criteria.htm). The third having died
aged 92 years, some 7 years after surgery, showing signs of dementia not ... Cited by 6 - Related articles - BL Direct - All 2 versions
- ►vetpathology.org JJ Greenlee, AN Hamir, MH West Greenlee - Veterinary Pathology Online, 2006 - Am Coll Vet Pathol The purpose of this study was to characterize the patterns of PrP Sc
immunoreactivity in the retinae of scrapie-affected sheep and to determine the
extent of retinal pathology as indicated by glial fibrillary acidic protein ... Cited by 6 - Related articles - BL Direct - All 15 versions
- ►sgmjournals.org AH Peden, DL Ritchie, HP Uddin, AF Dean, … - Journal of General Virology, 2007 - Soc General Microbiol By using high-sensitivity Western blotting and immunohistochemistry, pituitary
glands from patients with sporadic and variant Creutzfeldt–Jakob disease (sCJD
and vCJD, respectively) were analysed for the presence of the ... Cited by 4 - Related articles - BL Direct - All 5 versions
- ►amjpathol.org J Gong, A Jellali, V Forster, J Mutterer, E … - American Journal of Pathology, 2007 - ASIP In patients affected by Creutzfeldt-Jakob disease and in animals affected by
transmissible spongiform encephalopathies, retinal functions are altered, and
major spongiform changes are observed in the outer plexiform layer where ... Cited by 3 - Related articles - BL Direct - All 6 versions
T Hamaguchi, M Noguchi-Shinohara, Y …, 2007 - pubmedcentral.nih.gov Eleven (1.8%) of 597 patients underwent ophthalmic surgery within 1 month before
the onset of prion disease or after the onset. All ophthalmologists reused
surgical instruments that had been incompletely sterilized to eliminate ... Cited by 3 - Related articles - BL Direct - All 5 versions
- ►usda.gov [PDF] JD Smith, JJ Greenlee, AN Hamir, MH West … - Journal of Comparative Pathology, 2007 - Elsevier Transmissible spongiform encephalopathies (TSEs) are a group of fatal
neurodegenerative diseases characterized microscopically by spongiform lesions
(vacuolation) in the neuropil, neuronal loss, and gliosis. Accumulation of ... Cited by 3 - Related articles - All 11 versions
AH Peden, MW Head, M Jones, I MacGregor, M … - Expert Opin. Med. Diagn., 2008 - informahealthcare.com Variant Creutzfeldt–Jakob disease (vCJD) is a transmissible neurodegenerative
prion disease that continues to present a unique problem for medical
diagnostics. Uncertainties remain over the prevalence of vCJD in the UK ... Cited by 2 - Related articles - All 3 versions
WJ Armitage, AB Tullo, JW Ironside - Eye, 2009 - nature.com Creutzfeldt–Jakob disease (CJD) is a rare, fatal neurodegenerative disease
that occurs in sporadic, genetic, variant, and iatrogenic forms. The
transformation of normal prion protein (PrP C ) to the abnormal form (PrP ... Cited by 1 - Related articles - All 3 versions
J Kanazawa - origin.cdc.gov Visual impairment occurs in 10% to 20% of patients with sporadic
Creutzfeldt-Jakob disease (sCJD) dur- ing an early stage of the disease
(Heidenhain variant) (1,2). Some patients with prion diseases may visit ... Related articles - View as HTML - All 2 versions
MW Head, JW Ironside - Expert Review of Ophthalmology, 2008 - ingentaconnect.com Creutzfeldt–Jakob disease (CJD) belongs to the group of human prion diseases
– rare neurodegenerative disorders that are caused by transmissible agents
known as prions. In CJD, the levels of prion infectivity are highest in the ... Related articles - All 3 versions
