1. B. Meissner, K. Kallenberg, P. Sanchez-Juan, D. Collie, D. M. Summers, S. Almonti, S. J. Collins, P. Smith, P. Cras, G. H. Jansen, J. P. Brandel, M. B. Coulthart, H. Roberts, B. Van Everbroeck, D. Galanaud, V. Mellina, R. G. Will, and I. Zerr. MRI lesion profiles in sporadic Creutzfeldt-Jakob disease. Neurology, 72(23):1994-2001, 2009. Note: 121/7369/Department of Health/United KingdomJournal ArticleMulticenter StudyResearch Support, Non-U.S. Gov'tUnited States. [WWW] Keyword(s): Basal Ganglia/anatomy & histology/pathology/physiopathology, Brain/anatomy & histology/*pathology/physiopathology, Cerebral Cortex/anatomy & histology/pathology/physiopathology, Codon, Creutzfeldt-Jakob Syndrome/classification/genetics/*pathology, DNA Mutational Analysis, Diffusion Magnetic Resonance Imaging/methods, Disease Progression, Genetic Screening, Genotype, Humans, Magnetic Resonance Imaging/*methods, Nerve Fibers, Myelinated/pathology, Observer Variation, Odds Ratio, PrPSc Proteins/genetics, Predictive Value of Tests, Sensitivity and Specificity, Thalamus/anatomy & histology/pathology/physiopathology.



2. I. Zerr, K. Kallenberg, D. M. Summers, C. Romero, A. Taratuto, U. Heinemann, M. Breithaupt, D. Varges, B. Meissner, A. Ladogana, M. Schuur, S. Haik, S. J. Collins, G. H. Jansen, G. B. Stokin, J. Pimentel, E. Hewer, D. Collie, P. Smith, H. Roberts, J. P. Brandel, C. van Duijn, M. Pocchiari, C. Begue, P. Cras, R. G. Will, and P. Sanchez-Juan. Updated clinical diagnostic criteria for sporadic Creutzfeldt Jakob disease. Brain, 132(Pt 10):2659-68, 2009. Note: Journal articlea journal of neurology. [WWW]



3. S. J. Collins, P. Sanchez-Juan, C. L. Masters, G. M. Klug, C. van Duijn, A. Poleggi, M. Pocchiari, S. Almonti, N. Cuadrado-Corrales, J. de Pedro-Cuesta, H. Budka, E. Gelpi, M. Glatzel, M. Tolnay, E. Hewer, I. Zerr, U. Heinemann, H. A. Kretszchmar, G. H. Jansen, E. Olsen, E. Mitrova, A. Alperovitch, J. P. Brandel, J. Mackenzie, K. Murray, and R. G. Will. Determinants of diagnostic investigation sensitivities across the clinical spectrum of sporadic Creutzfeldt-Jakob disease. Brain, 129(Pt 9):2278-87, 2006. Note: Journal ArticleMulticenter StudyResearch Support, Non-U.S. Gov'tEnglanda journal of neurology. [WWW] Keyword(s): 14-3-3 Proteins/cerebrospinal fluid, Adult, Age of Onset, Aged, Aged, 80 and over, Brain/pathology, Creutzfeldt-Jakob Syndrome/cerebrospinal fluid/*diagnosis/genetics, Electroencephalography/methods, Female, Genotype, Humans, Magnetic Resonance Imaging/methods, Male, Middle Aged, Polymorphism, Genetic/genetics, Prions/genetics, Protein Precursors/genetics, Sensitivity and Specificity, Time Factors.

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