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Treatable neurological disorders misdiagnosed as Creutzfeldt‐Jakob disease N Chitravas, RS Jung, DM Kofskey, JE Blevins, P Gambetti, RJ Leigh, ... Annals of neurology 70 (3), 437-444, 2011 | 231 | 2011 |
Diagnostic and prognostic value of human prion detection in cerebrospinal fluid A Foutz, BS Appleby, C Hamlin, X Liu, S Yang, Y Cohen, W Chen, ... Annals of neurology 81 (1), 79-92, 2017 | 211 | 2017 |
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Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt–Jakob disease: its effect on the phenotype and prion-type characteristics I Cali, R Castellani, A Alshekhlee, Y Cohen, J Blevins, J Yuan, ... Brain 132 (10), 2643-2658, 2009 | 155 | 2009 |
Small Protease Sensitive Oligomers of PrPSc in Distinct Human Prions Determine Conversion Rate of PrPC C Kim, T Haldiman, K Surewicz, Y Cohen, W Chen, J Blevins, MS Sy, ... Public Library of Science 8 (8), e1002835, 2012 | 86 | 2012 |
Protease-Sensitive Conformers in Broad Spectrum of Distinct PrPSc Structures in Sporadic Creutzfeldt-Jakob Disease Are Indicator of Progression Rate C Kim, T Haldiman, Y Cohen, W Chen, J Blevins, MS Sy, M Cohen, ... PLoS pathogens 7 (9), e1002242, 2011 | 85 | 2011 |
Diagnosis of prion diseases by RT-QuIC results in improved surveillance DD Rhoads, A Wrona, A Foutz, J Blevins, K Glisic, M Person, RA Maddox, ... Neurology 95 (8), e1017-e1026, 2020 | 83 | 2020 |
Evaluation of a new criterion for detecting prion disease with diffusion magnetic resonance imaging A Bizzi, R Pascuzzo, J Blevins, M Grisoli, R Lodi, MEM Moscatelli, ... JAMA neurology 77 (9), 1141-1149, 2020 | 60 | 2020 |
Co-existence of distinct prion types enables conformational evolution of human PrPSc by competitive selection T Haldiman, C Kim, Y Cohen, W Chen, J Blevins, L Qing, ML Cohen, ... Journal of Biological Chemistry 288 (41), 29846-29861, 2013 | 59 | 2013 |
Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study E Jones, H Hummerich, E Viré, J Uphill, A Dimitriadis, H Speedy, ... The Lancet Neurology 19 (10), 840-848, 2020 | 50 | 2020 |
Prion disease incidence in the United States: 2003–2015 RA Maddox, MK Person, JE Blevins, JY Abrams, BS Appleby, ... Neurology 94 (2), e153-e157, 2020 | 43 | 2020 |
Subtype diagnosis of sporadic Creutzfeldt–Jakob disease with diffusion magnetic resonance imaging A Bizzi, R Pascuzzo, J Blevins, MEM Moscatelli, M Grisoli, R Lodi, ... Annals of Neurology 89 (3), 560-572, 2021 | 34 | 2021 |
Prion propagation estimated from brain diffusion MRI is subtype dependent in sporadic Creutzfeldt–Jakob disease R Pascuzzo, NP Oxtoby, AL Young, J Blevins, G Castelli, S Garbarino, ... Acta neuropathologica 140, 169-181, 2020 | 33 | 2020 |
A low-molecular-weight ferroxidase is increased in the CSF of sCJD cases: CSF ferroxidase and transferrin as diagnostic biomarkers for sCJD S Haldar, AJ Beveridge, J Wong, A Singh, D Galimberti, B Borroni, X Zhu, ... Antioxidants & Redox Signaling 19 (14), 1662-1675, 2013 | 27 | 2013 |
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019 neurogenic persistent genital arousal disorder (PGAD) secondary to radiculopathy of sacral spinal nerve roots (SSNR): treatment outcome following spine surgery C Kim, J Blevins, J Hanley, S Goldstein, B Komisaruk, I Goldstein The Journal of Sexual Medicine 16 (Supplement_3), S9-S9, 2019 | 11 | 2019 |
Human prion disease surveillance in Washington State, 2006-2017 L Sánchez-González, RA Maddox, LC Lewis, JE Blevins, EJ Harker, ... JAMA Network Open 3 (10), e2020690-e2020690, 2020 | 6 | 2020 |
Improving Creutzfeldt-Jakob disease incidence estimates by incorporating results of neuropathological analyses, United States, 2003-2011 R Maddox, M Person, A Minino, J Blevins, L Schonberger, E Belay Prion 9, S55-S56, 2015 | 5 | 2015 |
The co-existence of PrPSc type 1 and 2 in Sporadic Creutzfeldt-Jakob Disease affects the phenotype and PrPSc conformation I Cali, I Cohen, J Blevins, R Castellani, A Al-Shekhlee, J Yuan, P Parchi, ... Journal of Neuropathology and Experimental Neurology 68 (5), 553-553, 2009 | 5 | 2009 |