{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,17]],"date-time":"2026-08-17T12:27:54Z","timestamp":1786969674718,"version":"build-2736575974"},"reference-count":68,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"2","license":[{"start":{"date-parts":[[2026,5,1]],"date-time":"2026-05-01T00:00:00Z","timestamp":1777593600000},"content-version":"unspecified","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":["Ann Mov Disord"],"published-print":{"date-parts":[[2026,5]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>Prion disorders are rare neurodegenerative disorders resulting from proteinaceous infectious particles and are universally fatal. It can be sporadic, genetic, or acquired. Globally, sporadic Creutzfeldt-Jakob disease is the most commonly reported prion disorder, as well as in India. To delineate the Indian perspective, this study identified and analyzed Indian studies on Prion disorders using the PubMed and Scopus databases. Several Indian case reports and case series suggest a higher prevalence of prion disorders than expected. These disorders commonly affect individuals in the sixth decade of life or later. They are accompanied by rapidly progressive dementia and movement disorders in the form of myoclonus, ataxia, and parkinsonism. The diffusion-weighted sequence of brain magnetic resonance imaging has the highest sensitivity for confirming suspected prion disorders. Short-interval periodic complexes in electroencephalograms are a supportive feature for diagnosing these disorders. Although brain biopsy is the gold standard for their diagnosis, to date, this approach has been performed in &lt;50 Indian cases. Although the results of real-time quaking-induced conversion are comparable to those of histopathological diagnosis, it is not available in India. A pan-India prion disorder registry should be established for the extensive evaluation and systematic collection of data on prion disorders.<\/jats:p>","DOI":"10.4103\/aomd.aomd_93_25","type":"journal-article","created":{"date-parts":[[2026,6,1]],"date-time":"2026-06-01T14:00:37Z","timestamp":1780322437000},"page":"126-132","update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":0,"title":["Prion Disorders Update: An Indian Perspective"],"prefix":"10.4103","volume":"9","author":[{"given":"Taallapalli Ashok Vardhan","family":"Reddy","sequence":"first","affiliation":[{"name":"Department of Neurology, All India Institute of Medical Sciences, Bibinagar, Telangana, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sindhu","family":"Toomukuntla","sequence":"additional","affiliation":[{"name":"Department of Neurology, All India Institute of Medical Sciences, Bibinagar, Telangana, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Anshuman","family":"Pradhan","sequence":"additional","affiliation":[{"name":"Department of Neurology, All India Institute of Medical Sciences, Bibinagar, Telangana, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Niraj","family":"Kumar","sequence":"additional","affiliation":[{"name":"Department of Neurology, All India Institute of Medical Sciences, Bibinagar, Telangana, India"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","published-online":{"date-parts":[[2026,5,29]]},"reference":[{"key":"CIT0001-20260817","doi-asserted-by":"crossref","first-page":"e2","DOI":"10.1016\/S1473-3099(19)30615-2","article-title":"Creutzfeldt-Jakob disease: A systematic review of global incidence, prevalence, infectivity, and incubation","volume":"20","author":"Uttley","year":"2020","journal-title":"Lancet Infect Dis"},{"key":"CIT0002-20260817","doi-asserted-by":"crossref","first-page":"393","DOI":"10.1016\/B978-0-12-802395-2.00028-6","article-title":"Prion diseases","volume":"145","author":"Ironside","year":"2018","journal-title":"Handb Clin Neurol"},{"key":"CIT0003-20260817","doi-asserted-by":"crossref","first-page":"343","DOI":"10.1016\/j.brainresbull.2008.09.012","article-title":"The early history of the transmissible spongiform encephalopathies exemplified by scrapie","volume":"77","author":"Schneider","year":"2008","journal-title":"Brain Res Bull"},{"key":"CIT0004-20260817","doi-asserted-by":"crossref","first-page":"12439","DOI":"10.3390\/ijms222212439","article-title":"Virus infection, genetic mutations, and prion infection in prion protein conversion","volume":"22","author":"Hara","year":"2021","journal-title":"Int J Mol Sci"},{"key":"CIT0005-20260817","doi-asserted-by":"crossref","first-page":"2068","DOI":"10.1016\/S0140-6736(06)68930-7","article-title":"Kuru in the 21st century\u2014an acquired human prion disease with very long incubation periods","volume":"367","author":"Collinge","year":"2006","journal-title":"Lancet"},{"issue":"4542","key":"CIT0006-20260817","doi-asserted-by":"crossref","first-page":"136","DOI":"10.1126\/science.6801762","article-title":"Novel proteinaceous infectious particles cause scrapie","volume":"216","author":"Prusiner","year":"1982","journal-title":"Science"},{"key":"CIT0007-20260817","first-page":"439","article-title":"Jacob Crutzfeld syndrome. (A case report)","volume":"18","author":"Rao","year":"1965","journal-title":"Indian Pract"},{"key":"CIT0008-20260817","doi-asserted-by":"crossref","first-page":"93","DOI":"10.1159\/000110515","article-title":"Creutzfeldt-Jakob disease in Western India: Observations in 7 patients","volume":"2","author":"Singhal","year":"1983","journal-title":"Neuroepidemiology"},{"key":"CIT0009-20260817","doi-asserted-by":"crossref","first-page":"27","DOI":"10.1159\/000110244","article-title":"Creutzfeldt-Jakob disease in India (1971\u20131990)","volume":"10","author":"Satishchandra","year":"1991","journal-title":"Neuroepidemiology"},{"key":"CIT0010-20260817","first-page":"338","article-title":"Creutzfeldt-Jakob Disease: Report of 10 cases from North India","volume":"49","author":"Mehndiratta","year":"2001","journal-title":"Neurol India"},{"key":"CIT0011-20260817","doi-asserted-by":"crossref","first-page":"790","DOI":"10.1016\/S0140-6736(05)67193-0","article-title":"Did BSE in the UK originate from the Indian subcontinent?","volume":"366","author":"Shankar","year":"2005","journal-title":"Lancet"},{"key":"CIT0012-20260817","doi-asserted-by":"crossref","first-page":"438","DOI":"10.4103\/0253-7176.191376","article-title":"Creutzfeldt-Jakob disease phenotype and course: Our experience from a tertiary center","volume":"38","author":"Chandra","year":"2016","journal-title":"Indian J Psychol Med"},{"key":"CIT0013-20260817","doi-asserted-by":"crossref","first-page":"14","DOI":"10.5334\/tohm.753","article-title":"Spectrum and pattern of movement disorders in patients with sporadic Creutzfeldt-Jakob disease","volume":"13","author":"Gurram","year":"2023","journal-title":"Tremor Other Hyperkinet Mov (N Y)"},{"key":"CIT0014-20260817","doi-asserted-by":"crossref","first-page":"39","DOI":"10.4103\/0976-3147.143189","article-title":"A study of clinical profile, radiological and electroencephalographic characteristics of suspected Creutzfeldt-Jakob disease in a tertiary care centre in South India","volume":"6","author":"Mahale","year":"2015","journal-title":"J Neurosci Rural Pract"},{"key":"CIT0015-20260817","doi-asserted-by":"crossref","first-page":"659","DOI":"10.4103\/0972-2327.120486","article-title":"Case series of probable sporadic Creutzfeldt-Jakob disease from Eastern India","volume":"16","author":"Biswas","year":"2013","journal-title":"Ann Indian Acad Neurol"},{"key":"CIT0016-20260817","doi-asserted-by":"crossref","first-page":"e0189832","DOI":"10.1371\/journal.pone.0189832","article-title":"Rapidly progressive dementia: An eight year (2008\u20132016) retrospective study","volume":"13","author":"Anuja","year":"2018","journal-title":"PLoS One"},{"key":"CIT0017-20260817","doi-asserted-by":"crossref","first-page":"545","DOI":"10.32677\/IJCR.2020.v06.i10.001","article-title":"Clinical and magnetic resonance imaging features in sporadic Creutzfeldt\u2013Jakob disease: A case series of four patients","volume":"6","author":"Verma","year":"2020","journal-title":"Indian J Case Rep"},{"key":"CIT0018-20260817","first-page":"e50008","article-title":"A study of clinical profile, radiological and electroencephalographic characteristics of sporadic creutzfeldt-jakob disease from a tertiary care hospital","volume":"15","author":"Madineni","year":"2023","journal-title":"Cureus"},{"key":"CIT0019-20260817","doi-asserted-by":"crossref","first-page":"131","DOI":"10.4103\/aomd.aomd_118_24","article-title":"Case series of prion disease patients from Northern India: Insights from clinical, EEG, and imaging data","volume":"8","author":"Kumar","year":"2025","journal-title":"Ann Mov Disord"},{"key":"CIT0020-20260817","first-page":"548","article-title":"Stroke like presentation of Creutzfeldt Jakob disease: an unusual variant","volume":"47","author":"Panagariya","year":"1999","journal-title":"J Assoc Physicians India"},{"key":"CIT0021-20260817","doi-asserted-by":"crossref","DOI":"10.4103\/0971-3026.28737","article-title":"Creutzfeldt-Jakob disease-A case report","volume":"15","author":"Gupta","year":"2005","journal-title":"Indian J Radiol Imaging"},{"key":"CIT0022-20260817","doi-asserted-by":"crossref","first-page":"297","DOI":"10.1177\/197140090601900304","article-title":"Creutzfeldt-Jakob disease the value of diffusion-weighted MRI","volume":"19","author":"Purkayastha","year":"2006","journal-title":"Neuroradiol J"},{"key":"CIT0023-20260817","doi-asserted-by":"crossref","first-page":"418","DOI":"10.4103\/0028-3886.28119","article-title":"Sporadic onset Creutzfeldt-Jacob disease: Interesting MRI observations","volume":"54","author":"Praveen","year":"2006","journal-title":"Neurol India"},{"key":"CIT0024-20260817","first-page":"52","article-title":"Creutzfeldt-Jakob disease: Importance of early magnetic resonance imaging","volume":"12","author":"Madhusudhan","year":"2009","journal-title":"Ann Indian Acad Neurol"},{"key":"CIT0025-20260817","doi-asserted-by":"crossref","first-page":"427","DOI":"10.1093\/qjmed\/hcq061","article-title":"Rapidly progressive dementia and myoclonus","volume":"103","author":"Saifudheen","year":"2010","journal-title":"QJM"},{"key":"CIT0026-20260817","doi-asserted-by":"crossref","first-page":"97","DOI":"10.4103\/0377-4929.94871","article-title":"Creutzfeldt-Jacob disease: An autopsy case report in tertiary care hospital","volume":"55","author":"Gadgil","year":"2012","journal-title":"Indian J Pathol Microbiol"},{"key":"CIT0027-20260817","doi-asserted-by":"crossref","first-page":"E51","DOI":"10.1176\/appi.neuropsych.11080199","article-title":"New variant Creutzfeldt-Jacob Disease presenting with catatonia: A rare presentation","volume":"24","author":"Shekhawat","year":"2012","journal-title":"J Neuropsychiatry Clin Neurosci"},{"key":"CIT0028-20260817","doi-asserted-by":"crossref","first-page":"408","DOI":"10.4103\/0976-3147.102645","article-title":"Diffusion-weighted imaging: As the first diagnostic clue to Creutzfeldt Jacob disease","volume":"3","author":"Kumaran","year":"2012","journal-title":"J Neurosci Rural Pract"},{"key":"CIT0029-20260817","doi-asserted-by":"crossref","first-page":"31","DOI":"10.1016\/j.baga.2011.11.005","article-title":"Wrapping up a diagnosis of Creutzfeldt-Jakob disease with the \u201c cortical ribbon.\u201d","volume":"2","author":"de Souza","year":"2012","journal-title":"Basal Ganglia"},{"key":"CIT0030-20260817","first-page":"bcr2013203007","article-title":"Sporadic Creutzfeldt-Jakob disease (sCJD) with asymmetric findings","volume":"2014","author":"Khilari","year":"2014","journal-title":"Case Rep"},{"key":"CIT0031-20260817","doi-asserted-by":"crossref","first-page":"840","DOI":"10.4103\/0975-2870.169921","article-title":"Pulvinar\/hockey stick sign in Creutzfeldt-Jakob disease","volume":"8","author":"Venkatesan","year":"2015","journal-title":"Med J DY Patil Univ"},{"key":"CIT0032-20260817","doi-asserted-by":"crossref","first-page":"184","DOI":"10.4103\/IJPSYM.IJPSYM_102_18","article-title":"Creutzfeldt-Jacob disease with psychiatric presentation: Hen\u2019s teeth in Indian subcontinent: A case report","volume":"41","author":"Singh","year":"2019","journal-title":"Indian J Psychol Med"},{"key":"CIT0033-20260817","doi-asserted-by":"crossref","first-page":"94","DOI":"10.1002\/agm2.12057","article-title":"A case of rapidly progressive dementia: A diagnosis not to be missed","volume":"2","author":"Das","year":"2019","journal-title":"Aging Med (Milton)"},{"key":"CIT0034-20260817","doi-asserted-by":"crossref","first-page":"163","DOI":"10.1186\/s13256-019-2089-5","article-title":"Young-onset sporadic Creutzfeldt\u2013Jakob disease with atypical phenotypic features: A case report","volume":"13","author":"Lahiri","year":"2019","journal-title":"J Med Case Rep"},{"key":"CIT0035-20260817","doi-asserted-by":"crossref","first-page":"217","DOI":"10.4103\/0028-3886.310104","article-title":"A case of subacute progressive cerebellar ataxia: Brownell-Oppenheimer variant of sporadic Creutzfeldt-Jakob disease","volume":"69","author":"Pandey","year":"2021","journal-title":"Neurol India"},{"key":"CIT0036-20260817","doi-asserted-by":"crossref","first-page":"1012","DOI":"10.4103\/aian.AIAN_1069_20","article-title":"Creutzfeldt-Jakob disease in nonagenarian: A rare presentation from India","volume":"24","author":"Khichar","year":"2021","journal-title":"Ann Indian Acad Neurol"},{"key":"CIT0037-20260817","doi-asserted-by":"crossref","first-page":"e2024502","DOI":"10.4322\/acr.2024.502","article-title":"A rare case of Sporadic Creutzfeldt-Jakob disease at a remote mountain hospital in the Indian Himalayan Region","volume":"14","author":"Sharma","year":"2024","journal-title":"Autopsy Case Rep"},{"key":"CIT0038-20260817","first-page":"e63702","article-title":"Unusually late onset of Creutzfeldt-Jakob disease following COVID-19 infection in India: a case report","volume":"16","author":"Begum","year":"2024","journal-title":"Cureus"},{"key":"CIT0039-20260817","doi-asserted-by":"crossref","first-page":"95","DOI":"10.17816\/ACEN.977","article-title":"A man who changed six spectacles: A case of Heidenhain variant of the Creutzfeldt\u2013Jakob disease","volume":"18","author":"Thiruvuru","year":"2024","journal-title":"Ann Clin Exp Neurol"},{"key":"CIT0040-20260817","first-page":"e53","article-title":"Sporadic Creutzfeldt-Jakob disease: A rare case of rapid progressive cognitive decline with special reference to magnetic resonance spectroscopy","volume":"72","author":"Pandya","year":"2024","journal-title":"J Assoc Phys India"},{"key":"CIT0041-20260817","first-page":"193","article-title":"Improving laboratory diagnosis of Creutzfeldt-Jakob disease","volume":"36","author":"Masih","year":"2025","journal-title":"EJIFCC"},{"key":"CIT0042-20260817","doi-asserted-by":"crossref","first-page":"225","DOI":"10.4103\/aian.AIAN_441_18","article-title":"Familial Creutzfeldt\u2013Jakob disease: The first reported kindred from South-East Asia","volume":"22","author":"Sawal","year":"2019","journal-title":"Ann Indian Acad Neurol"},{"key":"CIT0043-20260817","doi-asserted-by":"crossref","first-page":"458","DOI":"10.4103\/aian.AIAN_214_19","article-title":"Familial Creutzfeldt-Jakob disease in an Indian kindred","volume":"22","author":"Katrak","year":"2019","journal-title":"Ann Indian Acad Neurol"},{"key":"CIT0044-20260817","doi-asserted-by":"crossref","first-page":"1431","DOI":"10.4103\/0028-3886.304068","article-title":"Familial Prion disease: First Indian Kindred with Gerstmann\u2013Str\u00e4ussler\u2013Scheinker syndrome","volume":"68","author":"Bhatia","year":"2020","journal-title":"Neurol India"},{"key":"CIT0045-20260817","doi-asserted-by":"crossref","first-page":"688","DOI":"10.1002\/mdc3.12999","article-title":"A case of autosomal dominant ataxia with vocal cord palsy attributed to a mutation in the PRNP Gene","volume":"7","author":"Kukkle","year":"2020","journal-title":"Mov Disord Clin Pract"},{"key":"CIT0046-20260817","doi-asserted-by":"crossref","first-page":"15","DOI":"10.31080\/ASNE.2021.04.0330","article-title":"Phenotypic variability and anticipation in a family of D178N-Familial Creutzfeldt-Jakob disease","volume":"4","author":"Sunny","year":"2021","journal-title":"Acta Sci Neurol"},{"key":"CIT0047-20260817","doi-asserted-by":"crossref","first-page":"795","DOI":"10.4103\/indianjpsychiatry.indianjpsychiatry_261_23","article-title":"Familial Creutzfeldt-Jakob Disease with early onset myoclonus: A case for fulminant progression","volume":"65","author":"Naskar","year":"2023","journal-title":"Indian J Psychiatry"},{"key":"CIT0048-20260817","doi-asserted-by":"crossref","first-page":"594","DOI":"10.4103\/aian.aian_870_23","article-title":"Familial Creutzfeldt\u2013Jakob Disease (CJD) kindred\u2013An unusual case report from India","volume":"27","author":"Sharma","year":"2024","journal-title":"Ann Indian Acad Neurol"},{"key":"CIT0049-20260817","doi-asserted-by":"crossref","first-page":"107218","DOI":"10.1016\/j.parkreldis.2024.107218","article-title":"Gerstmann-Straussler-Scheinker disease: Lessons from two new Indian kindreds","volume":"130","author":"Mustafa","year":"2025","journal-title":"Parkinsonism Relat Disord"},{"key":"CIT0050-20260817","doi-asserted-by":"crossref","first-page":"413","DOI":"10.3390\/brainsci14050413","article-title":"Interactions between cytokines and the pathogenesis of Prion diseases: Insights and implications","volume":"14","author":"Assis-de-Lemos","year":"2024","journal-title":"Brain Sci"},{"key":"CIT0051-20260817","doi-asserted-by":"crossref","first-page":"411","DOI":"10.4103\/0028-3886.181538","article-title":"A hospital-based registry of Creutzfeldt\u2013Jakob disease: Can neuroimaging serve as a surrogate biomarker?","volume":"64","author":"Divya","year":"2016","journal-title":"Neurol India"},{"key":"CIT0052-20260817","doi-asserted-by":"crossref","first-page":"760","DOI":"10.4103\/aian.AIAN_672_20","article-title":"EEG observations in probable sporadic CJD","volume":"23","author":"Mundlamurri","year":"2020","journal-title":"Ann Indian Acad Neurol"},{"key":"CIT0053-20260817","doi-asserted-by":"crossref","first-page":"205","DOI":"10.4103\/0972-2327.176867","article-title":"Development of a dot blot assay with antibodies to recombinant \u201ccore\u201d 14-3-3 protein: Evaluation of its usefulness in diagnosis of Creutzfeldt\u2013Jakob disease","volume":"19","author":"Subramanian","year":"2016","journal-title":"Ann Indian Acad Neurol"},{"key":"CIT0054-20260817","doi-asserted-by":"crossref","first-page":"154","DOI":"10.1016\/0022-510X(92)90046-N","article-title":"Histopathology and fine structure of the brain in six cases of Creutzfeldt-Jakob disease from western India","volume":"108","author":"Dastur","year":"1992","journal-title":"J Neurol Sci"},{"key":"CIT0055-20260817","doi-asserted-by":"crossref","first-page":"314","DOI":"10.1046\/j.1365-2990.2002.00399.x","article-title":"Brain biopsy in Creutzfeldt\u2013Jakob disease: evolution of pathological changes by prion protein immunochemistry","volume":"28","author":"Mahadevan","year":"2002","journal-title":"Neuropathol Appl Neurobiol"},{"key":"CIT0056-20260817","doi-asserted-by":"crossref","first-page":"1893","DOI":"10.1002\/mds.29152","article-title":"Prevalence and treatments of movement disorders in prion diseases: A longitudinal cohort study","volume":"37","author":"Sequeira","year":"2022","journal-title":"Mov Disord"},{"key":"CIT0057-20260817","first-page":"1551","article-title":"Diffusion-weighted and fluid-attenuated inversion recovery imaging in Creutzfeldt-Jakob disease: High sensitivity and specificity for diagnosis","volume":"26","author":"Young","year":"2005","journal-title":"Am J Neuroradiol"},{"key":"CIT0058-20260817","doi-asserted-by":"crossref","first-page":"1425","DOI":"10.1212\/WNL.0b013e3181a18846","article-title":"Pathologic correlates of diffusion MRI changes in Creutzfeldt-Jakob disease","volume":"72","author":"Manners","year":"2009","journal-title":"Neurology"},{"key":"CIT0059-20260817","doi-asserted-by":"crossref","first-page":"443","DOI":"10.1212\/01.WNL.0000134555.59460.5D","article-title":"Diffusion-weighted MRI abnormalities as an early diagnostic marker for Creutzfeldt\u2013Jakob disease","volume":"63","author":"Shiga","year":"2004","journal-title":"Neurology"},{"key":"CIT0060-20260817","doi-asserted-by":"crossref","first-page":"1412","DOI":"10.1016\/S0140-6736(00)02140-1","article-title":"The pulvinar sign on magnetic resonance imaging in variant Creutzfeldt-Jakob disease","volume":"355","author":"Zeidler","year":"2000","journal-title":"Lancet"},{"key":"CIT0061-20260817","doi-asserted-by":"crossref","first-page":"1711","DOI":"10.1212\/WNL.0b013e31821a4439","article-title":"Diffusion-weighted MRI hyperintensity patterns differentiate CJD from other rapid dementias","volume":"76","author":"Vitali","year":"2011","journal-title":"Neurology"},{"key":"CIT0062-20260817","doi-asserted-by":"crossref","first-page":"143","DOI":"10.1001\/archneur.1980.00500520041005","article-title":"Serial EEG findings in 27 cases of Creutzfeldt-Jakob disease","volume":"37","author":"Chiofalo","year":"1980","journal-title":"Arch Neurol"},{"key":"CIT0063-20260817","doi-asserted-by":"crossref","first-page":"637","DOI":"10.1212\/01.wnl.0000230159.67128.00","article-title":"CSF tests in the differential diagnosis of Creutzfeldt-Jakob disease","volume":"67","author":"Sanchez-Juan","year":"2006","journal-title":"Neurology"},{"key":"CIT0064-20260817","doi-asserted-by":"crossref","first-page":"1528","DOI":"10.1212\/WNL.56.11.1528","article-title":"CSF detection of the 14-3-3 protein in unselected patients with dementia","volume":"56","author":"Burkhard","year":"2001","journal-title":"Neurology"},{"key":"CIT0065-20260817","doi-asserted-by":"crossref","first-page":"924","DOI":"10.1056\/NEJM199609263351303","article-title":"The 14-3-3 brain protein in cerebrospinal fluid as a marker for transmissible spongiform encephalopathies","volume":"335","author":"Hsich","year":"1996","journal-title":"N Engl J Med"},{"key":"CIT0066-20260817","doi-asserted-by":"crossref","first-page":"473","DOI":"10.3390\/medicina58040473","article-title":"Role of biomarkers for the diagnosis of Prion diseases: A narrative review","volume":"58","author":"Altuna","year":"2022","journal-title":"Medicina (Kaunas)"},{"key":"CIT0067-20260817","doi-asserted-by":"crossref","first-page":"1324702","DOI":"10.3389\/fnmol.2024.1324702","article-title":"New implications for prion diseases therapy and prophylaxis","volume":"17","author":"Liu","year":"2024","journal-title":"Front Mol Neurosci"},{"key":"CIT0068-20260817","doi-asserted-by":"crossref","first-page":"2348","DOI":"10.1093\/brain\/awh249","article-title":"Predictors of survival in sporadic Creutzfeldt\u2013Jakob disease and other human transmissible spongiform encephalopathies","volume":"127","author":"Pocchiari","year":"2004","journal-title":"Brain"}],"container-title":["Annals of Movement Disorders"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.ovid.com\/10.4103\/aomd.aomd_93_25","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,8,17]],"date-time":"2026-08-17T12:02:08Z","timestamp":1786968128000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.ovid.com\/10.4103\/aomd.aomd_93_25"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2026,5]]},"references-count":68,"journal-issue":{"issue":"2","published-print":{"date-parts":[[2026]]}},"URL":"https:\/\/doi.org\/10.4103\/aomd.aomd_93_25","relation":{},"ISSN":["2590-3446","2590-3454"],"issn-type":[{"value":"2590-3446","type":"print"},{"value":"2590-3454","type":"electronic"}],"subject":[],"published":{"date-parts":[[2026,5]]},"assertion":[{"value":"2025-11-13","name":"received","label":"Received","group":{"name":"publication_history","label":"Publication History"}},{"value":"2026-03-09","name":"accepted","label":"Accepted","group":{"name":"publication_history","label":"Publication History"}}]}}