Detection of prion infection in variant Creutzfeldt-Jakob disease: a blood-based assay von Edgeworth, Julie Ann, PhD, Farmer, Michael, BSc, Sicilia, Anita, MSc, Tavares, Paul, MSc, Beck, Jonathan, BSc, Campbell, Tracy, BSc, Lowe, Jessica, BSc, Mead, Simon, PhD, Rudge, Peter, FRCP, Collinge, John, Prof, Jackson, Graham S, Dr

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Safety and efficacy of quinacrine in human prion disease (PRION-1 study): a patient-preference trial von Collinge, John, MD, Gorham, Michele, RN, Hudson, Fleur, BA, Kennedy, Angus, MD, Keogh, Geraldine, Pal, Suvankar, MRCP, Rossor, Martin, MD, Rudge, Peter, FRCP, Siddique, Durre, PhD, Spyer, Moira, PhD, Thomas, Dafydd, MD, Walker, Sarah, PhD, Webb, Tom, BSc, Wroe, Steve, MD, Darbyshire, Janet, FRCP

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Infratentorial superficial siderosis: Classification, diagnostic criteria, and rational investigation pathway von Wilson, Duncan, Chatterjee, Fiona, Farmer, Simon F., Rudge, Peter, McCarron, Mark O., Cowley, Peter, Werring, David J.

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The language disorder of prion disease is characteristic of a dynamic aphasia and is rarely an isolated clinical feature von Caine, Diana, Nihat, Akin, Crabb, Philippa, Rudge, Peter, Cipolotti, Lisa, Collinge, John, Mead, Simon

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Clinical Trial Simulations Based on Genetic Stratification and the Natural History of a Functional Outcome Measure in Creutzfeldt-Jakob Disease von Mead, Simon, Burnell, Matthew, Lowe, Jessica, Thompson, Andrew, Lukic, Ana, Porter, Marie-Claire, Carswell, Christopher, Kaski, Diego, Kenny, Janna, Mok, Tze How, Bjurstrom, Nina, Franko, Edit, Gorham, Michele, Druyeh, Ronald, Wadsworth, Jonathan D. F, Jaunmuktane, Zane, Brandner, Sebastian, Hyare, Harpreet, Rudge, Peter, Walker, A. Sarah, Collinge, John

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The Medical Research Council Prion Disease Rating Scale: a new outcome measure for prion disease therapeutic trials developed and validated using systematic observational studies von THOMPSON, Andrew G. B, LOWE, Jessica, COLLINGE, John, MEAD, Simon, FOX, Zoe, LUKIC, Ana, PORTER, Marie-Claire, FORD, Liz, GORHAM, Michele, GOPALAKRISHNAN, Gosala S, RUDGE, Peter, SARAH WALKER, A

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Variant CJD in an individual heterozygous for PRNP codon 129 von Kaski, Diego, MRCP, Mead, Simon, PhD, Hyare, Harpreet, FRCR, Cooper, Sarah, MRCP, Jampana, Ravi, FRCR, Overell, James, FRCP, Knight, Richard, FRCP, Collinge, John, Prof, Rudge, Peter, FRCP

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MRI findings are often missed in the diagnosis of Creutzfeldt-Jakob disease von Carswell, Christopher, Thompson, Andrew, Lukic, Ana, Stevens, John, Rudge, Peter, Mead, Simon, Collinge, John, Hyare, Harpreet

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Recollection and familiarity in dense hippocampal amnesia: A case study von Cipolotti, Lisa, Bird, Chris, Good, Tina, Macmanus, David, Rudge, Peter, Shallice, Tim

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Predictive testing for inherited prion disease: report of 22 years experience von Owen, Jane, Beck, Jon, Campbell, Tracy, Adamson, Gary, Gorham, Michele, Thompson, Andrew, Smithson, Sarah, Rosser, Elizabeth, Rudge, Peter, Collinge, John, Mead, Simon

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Zidovudine plus lamivudine in Human T-Lymphotropic Virus type-I-associated myelopathy: a randomised trial von Taylor, Graham P, Goon, Peter, Furukawa, Yoshitaka, Green, Hannah, Barfield, Anna, Mosley, Angelina, Nose, Hirohisa, Babiker, Abdel, Rudge, Peter, Usuku, Koichiro, Osame, Mitsuhiro, Bangham, Charles R M, Weber, Jonathan N

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Neuroanatomical correlates of prion disease progression - a 3T longitudinal voxel-based morphometry study von De Vita, Enrico, Ridgway, Gerard R, White, Mark J, Porter, Marie-Claire, Caine, Diana, Rudge, Peter, Collinge, John, Yousry, Tarek A, Jager, Hans Rolf, Mead, Simon, Thornton, John S, Hyare, Harpreet

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Neuronal antibodies in patients with suspected or confirmed sporadic Creutzfeldt-Jakob disease von Rossi, Meghan, Mead, Simon, Collinge, John, Rudge, Peter, Vincent, Angela

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Evidence for human transmission of amyloid-β pathology and cerebral amyloid angiopathy von Jaunmuktane, Zane, Mead, Simon, Ellis, Matthew, Wadsworth, Jonathan D. F., Nicoll, Andrew J., Kenny, Joanna, Launchbury, Francesca, Linehan, Jacqueline, Richard-Loendt, Angela, Walker, A. Sarah, Rudge, Peter, Collinge, John, Brandner, Sebastian

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Prevalence and Treatments of Movement Disorders in Prion Diseases: A Longitudinal Cohort Study von Sequeira, Danielle, Nihat, Akin, Mok, Tzehow, Coysh, Thomas, Rudge, Peter, Collinge, John, Mead, Simon

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Transmission of amyloid-β protein pathology from cadaveric pituitary growth hormone von Purro, Silvia A., Farrow, Mark A., Linehan, Jacqueline, Nazari, Tamsin, Thomas, David X., Chen, Zhicheng, Mengel, David, Saito, Takashi, Saido, Takaomi, Rudge, Peter, Brandner, Sebastian, Walsh, Dominic M., Collinge, John

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Iatrogenic Alzheimer’s disease in recipients of cadaveric pituitary-derived growth hormone von Banerjee, Gargi, Farmer, Simon F., Hyare, Harpreet, Jaunmuktane, Zane, Mead, Simon, Ryan, Natalie S., Schott, Jonathan M., Werring, David J., Rudge, Peter, Collinge, John

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Estimation of the number of inherited prion disease mutation carriers in the UK von Corbie, Rosie, Campbell, Tracy, Darwent, Lee, Rudge, Peter, Collinge, John, Mead, Simon

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Assessing initial MRI reports for suspected CJD patients von Jesuthasan, Aaron, Sequeira, Danielle, Hyare, Harpreet, Odd, Hans, Rudge, Peter, Mok, Tze How, Nihat, Akin, Collinge, John, Mead, Simon

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Are multiplication facts implemented by the left supramarginal and angular gyri? von van Harskamp, Natasja J, Rudge, Peter, Cipolotti, Lisa

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