Results 91 to 100 of about 12,633 (172)
BMC Microbiology, 2007 Background The human bacterial pathogen Campylobacter jejuni contains two subspecies: C. jejuni subsp. jejuni (Cjj) and C. jejuni subsp. doylei (Cjd). Although Cjd strains are isolated infrequently in many parts of the world, they are obtained primarily ...
Heath Sekou +3 more
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Creutzfeldt-Jacob Disease (CJD) : Report of 10 Cases from North India [PDF]
, 2002 I read with interest the article on 'Creutz-Jacob Disease (CJD) : Report of 10 cases from North India'.1 As the authors have remarked, CJD is being increasingly reported from various regions in India.
B. S. Singhal
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Counselling people with Creutzfeldt-Jakob Disease (CJD) and their families
, 2010 This article gives an account of the counselling service for people with Creutzfeldt-Jakob Disease (CJD) at the National Prion Clinic which is based in the National Hospital for Neurology and Neurosurgery in the UK and aims to provide information ...
Clare Morris
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Normalization of 14-3-3 in CJD
, 2008 We report on a 47-year-old woman with autopsy proven Creutzfeldt-Jakob disease (CJD), who had a positive initial 14-3-3 test but a subsequent negative test under pharmacologic suppression of the periodic epileptiform discharges on EEG.
Schrooten, Maarten +4 more
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Examples of patients with vCJD, sCJD and non-CJD diagnoses.
, 2018 Axial T2-weighted images of post-mortem brains from patients with suspected CJD, imaged using 1.0T Siemens Magnetom, with corresponding immunohistochemistry.
Jonathan Best (2043796) +8 more
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Clinical Parkinsonism & Related DisordersCreutzfeldt-Jakob disease (CJD) is a rare, rapidly progressive neurodegenerative disorder, characterized by the accumulation of abnormal prion proteins in the brain.
Matteo Costanzo +5 more
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Diffusion MR imaging in sporadic Creutzfeldt-Jakob disease
Çukurova Üniversitesi Tıp Fakültesi Dergisi, 2014 Creutzfeldt-Jakob disease (CJD) is a rare dementing disease and is thought to caused by a prion. It is characterized by rapidly progressive dementia, ataxia, myoclonus, akinetic mutism and eventual death.
Burcak Cakir Pekoz +4 more
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, 2015 * Tg27 = 102LL Tg27† Tg35c = 129MM Tg35 mice congenic on FVB/N genetic background.‡ Glycoform ratios of PrPSc propagated in transgenic mice (n = 4 per line) inoculated with Tg27-passaged classical CJD and IPD P102L prions has been compared with the human
Asif Jeelani (463648) +12 more
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Retinal Angiographic Evidence of CJD Prion Disease in Humans
, 2018 We report a unique case of retinal angiographic evidence of CJD prion disease, which, to our knowledge has not previously been reported. Significant retinal changes have been reported in the Veterinary literature and also on post-mortem human donor ...
Norah S. Lincoff; Lucia Balos; Charles Chung; Osman Farooq
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