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            "abstractNote": "Discovery oa a second affected branch of a family with transmitted Creutzfeldt-Jakob disease (CJD), originally reported by Buge et al. in 1978,  brings the total number of cases to 14 in 3 generations, with at least 20 members  of the next young adult generation presently at risk. Complete segregation of the  illness to the descendants of these 2 branches, with no skipped generations, and  an overall frequency of CJD in affected sibships of 56%, clearly defines a  pattern of autosomal dominance. The disease is indifferent to sex, either in  terms of affected members (8 males and 6 females) or of lineage (3 fathers and 3  mothers). Acquisition of CJD virus from a point source contamination is unlikely,  and case-to-case transmission, if it occurred, would have required an average  minimum incubation period of 17 years.",
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            "date": "1973 Nov",
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                },
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                    "tag": "Virus Diseases/complications"
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            "title": "Evidence for case-to-case transmission of Creutzfeldt-Jakob disease.",
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                    "lastName": "Will"
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            "abstractNote": "A Finnish family is described with 9 cases of presenile dementia in 3 generations. The mean age at onset was 52 years (range 46--62 years). Progressive  dementia, upper motor neuron signs, muscular rigidity, and twitching, irregular  tremors were consistent features in the 6 clinically investigated patients and  were associated with spongiform change in the cerebral cortex of one autopsy and  two brain biopsy cases. The EEG showed progressive slowing without the occurrence  of repetitive high-voltage complexes at any stage of the disease. The average  duration of the disease (21 months, range 11--36 months) was longer than in the  sporadic form of CJD. The occurrence of CJD within this family follows a pattern  consistent with an autosomal dominant mode of inheritance, suggesting the  possibility of vertical transmission of the presumptive causative agent for  example by genomic integration or transplacental passage. However, the occurrence  of the disease only through the paternal line of relationships and the presence  of a discordant twin pair argue strongly against transplacental passage or  transmission via mother's milk. Simple contact infection also seems unlikely, as  conjugal cases were not found among the 7 married patients. The interval between  the death of the last affected member in generation IV and the time of onset of  the disease in the first affected member of generation V was 10 years. Thus  setting a minimum incubation period if case-to-case transmission were occurring.  To evaluate the role of a genetically determined susceptibility to infection  studies on the HLA antigens and other genetic markers are in progress.",
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                    "lastName": "Kroupova"
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            "publicationTitle": "British medical journal (Clinical research ed.)",
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            "date": "1981 Feb 14",
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            "parsedDate": "1975-03",
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            "itemType": "journalArticle",
            "title": "Epidemiology of Creutzfeldt-Jakob disease in England and Wales.",
            "creators": [
                {
                    "creatorType": "author",
                    "firstName": "W. B.",
                    "lastName": "Matthews"
                }
            ],
            "abstractNote": "Some aspects of the epidemiology of Creutzfeldt-Jakob disease in England and Wales in the decade 1964-73 were studied with the object of detecting evidence of  natural transmission of this slow virus encephalopathy. Some geographical  clustering and possibility of contact between cases was found.",
            "publicationTitle": "Journal of neurology, neurosurgery, and psychiatry",
            "publisher": "",
            "place": "England",
            "date": "1975 Mar",
            "volume": "38",
            "issue": "3",
            "section": "",
            "partNumber": "",
            "partTitle": "",
            "pages": "210-213",
            "series": "",
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            "journalAbbreviation": "J Neurol Neurosurg Psychiatry",
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            "PMCID": "PMC491897",
            "ISSN": "0022-3050 1468-330X",
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            "language": "eng",
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                {
                    "tag": "Adult"
                },
                {
                    "tag": "Aged"
                },
                {
                    "tag": "Animals"
                },
                {
                    "tag": "Cerebrovascular Disorders/complications"
                },
                {
                    "tag": "Craniocerebral Trauma/complications"
                },
                {
                    "tag": "Creutzfeldt-Jakob Syndrome/*epidemiology/transmission"
                },
                {
                    "tag": "England"
                },
                {
                    "tag": "Feeding Behavior"
                },
                {
                    "tag": "Female"
                },
                {
                    "tag": "Ferrets"
                },
                {
                    "tag": "Humans"
                },
                {
                    "tag": "Male"
                },
                {
                    "tag": "Middle Aged"
                },
                {
                    "tag": "Rural Population"
                },
                {
                    "tag": "Trigeminal Neuralgia/surgery"
                },
                {
                    "tag": "Urban Population"
                },
                {
                    "tag": "Wales"
                }
            ],
            "collections": [
                "344H8INJ"
            ],
            "relations": {},
            "dateAdded": "2026-07-09T16:28:02Z",
            "dateModified": "2026-07-09T16:28:02Z"
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        "key": "K7T4UPBU",
        "version": 206436,
        "library": {
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            "creatorSummary": "Goldfarb et al.",
            "parsedDate": "1990-08-25",
            "numChildren": 0
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            "key": "K7T4UPBU",
            "version": 206436,
            "itemType": "journalArticle",
            "title": "Mutation in codon 200 of scrapie amyloid protein gene in two clusters of Creutzfeldt-Jakob disease in Slovakia.",
            "creators": [
                {
                    "creatorType": "author",
                    "firstName": "L. G.",
                    "lastName": "Goldfarb"
                },
                {
                    "creatorType": "author",
                    "firstName": "E.",
                    "lastName": "Mitrová"
                },
                {
                    "creatorType": "author",
                    "firstName": "P.",
                    "lastName": "Brown"
                },
                {
                    "creatorType": "author",
                    "firstName": "B. K.",
                    "lastName": "Toh"
                },
                {
                    "creatorType": "author",
                    "firstName": "D. C.",
                    "lastName": "Gajdusek"
                }
            ],
            "abstractNote": "",
            "publicationTitle": "Lancet (London, England)",
            "publisher": "",
            "place": "England",
            "date": "1990 Aug 25",
            "volume": "336",
            "issue": "8713",
            "section": "",
            "partNumber": "",
            "partTitle": "",
            "pages": "514-515",
            "series": "",
            "seriesTitle": "",
            "seriesText": "",
            "journalAbbreviation": "Lancet",
            "DOI": "10.1016/0140-6736(90)92073-q",
            "citationKey": "",
            "url": "",
            "accessDate": "",
            "PMID": "1975028",
            "PMCID": "",
            "ISSN": "0140-6736",
            "archive": "",
            "archiveLocation": "",
            "shortTitle": "",
            "language": "eng",
            "libraryCatalog": "",
            "callNumber": "",
            "rights": "",
            "extra": "",
            "tags": [
                {
                    "tag": "*Mutation"
                },
                {
                    "tag": "Aged"
                },
                {
                    "tag": "Codon/*genetics"
                },
                {
                    "tag": "Creutzfeldt-Jakob Syndrome/epidemiology/*genetics"
                },
                {
                    "tag": "Czechoslovakia/epidemiology"
                },
                {
                    "tag": "DNA, Viral/analysis"
                },
                {
                    "tag": "Female"
                },
                {
                    "tag": "Humans"
                },
                {
                    "tag": "Nerve Tissue Proteins/*genetics"
                },
                {
                    "tag": "PrP 27-30 Protein"
                },
                {
                    "tag": "RNA, Messenger/*genetics"
                },
                {
                    "tag": "Space-Time Clustering"
                }
            ],
            "collections": [
                "344H8INJ"
            ],
            "relations": {},
            "dateAdded": "2026-07-09T16:28:02Z",
            "dateModified": "2026-07-09T16:28:02Z"
        }
    },
    {
        "key": "ED7T3U75",
        "version": 206435,
        "library": {
            "type": "user",
            "id": 6212901,
            "name": "Nick Petosky",
            "links": {
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        },
        "meta": {
            "creatorSummary": "Barash and Dziura",
            "parsedDate": "2007-07",
            "numChildren": 0
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        "data": {
            "key": "ED7T3U75",
            "version": 206435,
            "itemType": "journalArticle",
            "title": "A systematic review of sporadic Creutzfeldt-Jakob disease clusters: do clinical, epidemiologic, and genetic features reflect infectious clustering mechanisms?",
            "creators": [
                {
                    "creatorType": "author",
                    "firstName": "Jed A.",
                    "lastName": "Barash"
                },
                {
                    "creatorType": "author",
                    "firstName": "James",
                    "lastName": "Dziura"
                }
            ],
            "abstractNote": "BACKGROUND: While the cause of sporadic Creutzfeldt-Jakob disease (sCJD) is unknown, case clustering could suggest infectious transmission in some instances.  METHODS: Publications of sCJD clusters were systematically identified and pooled  to determine if their clinical, epidemiologic, and genetic features reflected  potential infectious clustering mechanisms. RESULTS: The search yielded five  clusters involving 23 cases. Most notably, among 12 cases with reported  residential histories, patients lived for a median of 30.0 years (25th  percentile: 26.5 years; 75th percentile: 51.0 years) in their respective cluster  regions. Of 19 cases that underwent genotyping for polymorphic codon 129,  seventeen were methionine homozygotes (89.5%; 95% CI 67.4-98.3%); none were  heterozygous. CONCLUSIONS: Prolonged residency duration and Prnp codon 129  methionine homozygosity may be consistent with underlying disease-clustering  mechanisms, although larger, controlled investigations might help to exclude the  possibility that these findings reflect the normal distribution of these features  among relevant comparison populations.",
            "publicationTitle": "Connecticut medicine",
            "publisher": "",
            "place": "United States",
            "date": "2007 Jun-Jul",
            "volume": "71",
            "issue": "6",
            "section": "",
            "partNumber": "",
            "partTitle": "",
            "pages": "333-337",
            "series": "",
            "seriesTitle": "",
            "seriesText": "",
            "journalAbbreviation": "Conn Med",
            "DOI": "",
            "citationKey": "",
            "url": "",
            "accessDate": "",
            "PMID": "17619468",
            "PMCID": "",
            "ISSN": "0010-6178",
            "archive": "",
            "archiveLocation": "",
            "shortTitle": "",
            "language": "eng",
            "libraryCatalog": "",
            "callNumber": "",
            "rights": "",
            "extra": "",
            "tags": [
                {
                    "tag": "Cluster Analysis"
                },
                {
                    "tag": "Creutzfeldt-Jakob Syndrome/*epidemiology/genetics/transmission"
                },
                {
                    "tag": "Genotype"
                },
                {
                    "tag": "Humans"
                },
                {
                    "tag": "Residence Characteristics"
                },
                {
                    "tag": "Risk Factors"
                },
                {
                    "tag": "Time Factors"
                }
            ],
            "collections": [
                "344H8INJ"
            ],
            "relations": {},
            "dateAdded": "2026-07-09T16:28:02Z",
            "dateModified": "2026-07-09T16:28:02Z"
        }
    },
    {
        "key": "WQCXCXJ9",
        "version": 206434,
        "library": {
            "type": "user",
            "id": 6212901,
            "name": "Nick Petosky",
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        },
        "meta": {
            "creatorSummary": "Lo Russo et al.",
            "parsedDate": "1980-06",
            "numChildren": 0
        },
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            "key": "WQCXCXJ9",
            "version": 206434,
            "itemType": "journalArticle",
            "title": "Creutzfeldt-Jakob disease and sheep brain. A report from central and Southern Italy.",
            "creators": [
                {
                    "creatorType": "author",
                    "firstName": "F.",
                    "lastName": "Lo Russo"
                },
                {
                    "creatorType": "author",
                    "firstName": "G.",
                    "lastName": "Neri"
                },
                {
                    "creatorType": "author",
                    "firstName": "L.",
                    "lastName": "Figà-Talamanca"
                }
            ],
            "abstractNote": "The places of origin of 7 out of 8 patients with CJD coincide with the distribution of sheep-rearing in central and southern Italy, confirming the  suggested link between this disease and eating and-or handling sheep CNS tissue.  Since 6 of the 8 cases were women, it seems more likely that the virus  responsible for CJD enters the body through a break in the skin of the hands and  forearms in the process of foodhandling rather than via the Digestive tract. This  aspect should be borne in mind when investigating the problems of CJD  transmission.",
            "publicationTitle": "Italian journal of neurological sciences",
            "publisher": "",
            "place": "Italy",
            "date": "1980 Jun",
            "volume": "1",
            "issue": "3",
            "section": "",
            "partNumber": "",
            "partTitle": "",
            "pages": "171-174",
            "series": "",
            "seriesTitle": "",
            "seriesText": "",
            "journalAbbreviation": "Ital J Neurol Sci",
            "DOI": "10.1007/BF02335847",
            "citationKey": "",
            "url": "",
            "accessDate": "",
            "PMID": "7042643",
            "PMCID": "",
            "ISSN": "0392-0461",
            "archive": "",
            "archiveLocation": "",
            "shortTitle": "",
            "language": "eng",
            "libraryCatalog": "",
            "callNumber": "",
            "rights": "",
            "extra": "",
            "tags": [
                {
                    "tag": "*Animal Husbandry"
                },
                {
                    "tag": "*Food Handling"
                },
                {
                    "tag": "*Sheep"
                },
                {
                    "tag": "Aged"
                },
                {
                    "tag": "Animals"
                },
                {
                    "tag": "Brain"
                },
                {
                    "tag": "Creutzfeldt-Jakob Syndrome/epidemiology/*transmission"
                },
                {
                    "tag": "Diet/adverse effects"
                },
                {
                    "tag": "Female"
                },
                {
                    "tag": "Humans"
                },
                {
                    "tag": "Italy"
                },
                {
                    "tag": "Male"
                },
                {
                    "tag": "Middle Aged"
                },
                {
                    "tag": "Sheep Diseases/*transmission"
                }
            ],
            "collections": [
                "344H8INJ"
            ],
            "relations": {},
            "dateAdded": "2026-07-09T16:28:02Z",
            "dateModified": "2026-07-09T16:28:02Z"
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        "key": "4RM3EKR2",
        "version": 206433,
        "library": {
            "type": "user",
            "id": 6212901,
            "name": "Nick Petosky",
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            "creatorSummary": "Bacchetti",
            "parsedDate": "2003-12",
            "numChildren": 0
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            "key": "4RM3EKR2",
            "version": 206433,
            "itemType": "journalArticle",
            "title": "Age and variant Creutzfeldt-Jakob disease.",
            "creators": [
                {
                    "creatorType": "author",
                    "firstName": "Peter",
                    "lastName": "Bacchetti"
                }
            ],
            "abstractNote": "The young and stable median age of those who die of variant Creutzfeldt-Jakob disease has been attributed to age-dependent infection rates. This analysis shows  that an influence of age on risk for death after infection better explains age  patterns, suggesting that biologic factors peaking in the third decade of life  may hasten disease.",
            "publicationTitle": "Emerging infectious diseases",
            "publisher": "",
            "place": "United States",
            "date": "2003 Dec",
            "volume": "9",
            "issue": "12",
            "section": "",
            "partNumber": "",
            "partTitle": "",
            "pages": "1611-1612",
            "series": "",
            "seriesTitle": "",
            "seriesText": "",
            "journalAbbreviation": "Emerg Infect Dis",
            "DOI": "10.3201/eid0912.030361",
            "citationKey": "",
            "url": "",
            "accessDate": "",
            "PMID": "14720404",
            "PMCID": "",
            "ISSN": "1080-6040",
            "archive": "",
            "archiveLocation": "",
            "shortTitle": "",
            "language": "eng",
            "libraryCatalog": "",
            "callNumber": "",
            "rights": "",
            "extra": "",
            "tags": [
                {
                    "tag": "Adult"
                },
                {
                    "tag": "Age Factors"
                },
                {
                    "tag": "Creutzfeldt-Jakob Syndrome/*epidemiology/mortality"
                },
                {
                    "tag": "Humans"
                },
                {
                    "tag": "Models, Biological"
                }
            ],
            "collections": [
                "344H8INJ"
            ],
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            "dateAdded": "2026-07-09T16:28:02Z",
            "dateModified": "2026-07-09T16:28:02Z"
        }
    },
    {
        "key": "35EFWLQA",
        "version": 206432,
        "library": {
            "type": "user",
            "id": 6212901,
            "name": "Nick Petosky",
            "links": {
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                    "href": "https://www.zotero.org/foxsayswhat",
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        "meta": {
            "creatorSummary": "Cathala et al.",
            "parsedDate": "1985-06",
            "numChildren": 0
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        "data": {
            "key": "35EFWLQA",
            "version": 206432,
            "itemType": "journalArticle",
            "title": "Failure to detect scrapie virus in sheep at slaughter in a highly endemic region of France.",
            "creators": [
                {
                    "creatorType": "author",
                    "firstName": "F.",
                    "lastName": "Cathala"
                },
                {
                    "creatorType": "author",
                    "firstName": "P.",
                    "lastName": "Brown"
                },
                {
                    "creatorType": "author",
                    "firstName": "F.",
                    "lastName": "Gray"
                },
                {
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                    "firstName": "M.",
                    "lastName": "Sulima"
                },
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                    "creatorType": "author",
                    "firstName": "J.",
                    "lastName": "Chatelain"
                },
                {
                    "creatorType": "author",
                    "firstName": "C. J. Jr",
                    "lastName": "Gibbs"
                }
            ],
            "abstractNote": "A study was carried out in a sheep slaughterhouse located in a region of France where scrapie has been endemic for several decades. Neuropathological examination  of 63 randomly selected lambs and adult sheep revealed no scrapie-related  abnormalities, and inoculation of mice with brain, tonsil, lateropharyngeal  ganglia, and intestine from the same animals did not transmit scrapie. The  failure to detect any evidence of scrapie infection in commercially-bred sheep,  the absence of an increased mortality rate for human CJD in the surrounding  consumer region, and the absence of a single case of CJD among slaughterhouse  personnel, do not support the hypothesis that exposure to potentially  scrapie-contaminated products is responsible for CJD in humans.",
            "publicationTitle": "European journal of epidemiology",
            "publisher": "",
            "place": "Netherlands",
            "date": "1985 Jun",
            "volume": "1",
            "issue": "2",
            "section": "",
            "partNumber": "",
            "partTitle": "",
            "pages": "90-93",
            "series": "",
            "seriesTitle": "",
            "seriesText": "",
            "journalAbbreviation": "Eur J Epidemiol",
            "DOI": "10.1007/BF00141798",
            "citationKey": "",
            "url": "",
            "accessDate": "",
            "PMID": "3939516",
            "PMCID": "",
            "ISSN": "0393-2990",
            "archive": "",
            "archiveLocation": "",
            "shortTitle": "",
            "language": "eng",
            "libraryCatalog": "",
            "callNumber": "",
            "rights": "",
            "extra": "",
            "tags": [
                {
                    "tag": "*Abattoirs"
                },
                {
                    "tag": "Animals"
                },
                {
                    "tag": "Brain/pathology"
                },
                {
                    "tag": "Creutzfeldt-Jakob Syndrome/transmission"
                },
                {
                    "tag": "France"
                },
                {
                    "tag": "Humans"
                },
                {
                    "tag": "Mice"
                },
                {
                    "tag": "Prions/*isolation & purification"
                },
                {
                    "tag": "Scrapie/*epidemiology"
                },
                {
                    "tag": "Sheep/*microbiology"
                }
            ],
            "collections": [
                "344H8INJ"
            ],
            "relations": {},
            "dateAdded": "2026-07-09T16:28:02Z",
            "dateModified": "2026-07-09T16:28:02Z"
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    },
    {
        "key": "T7IDLY6D",
        "version": 206431,
        "library": {
            "type": "user",
            "id": 6212901,
            "name": "Nick Petosky",
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        "meta": {
            "creatorSummary": "Ward et al.",
            "parsedDate": "2002-08-27",
            "numChildren": 0
        },
        "data": {
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            "version": 206431,
            "itemType": "journalArticle",
            "title": "Sporadic Creutzfeldt-Jakob disease and surgery: a case-control study using community controls.",
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                {
                    "creatorType": "author",
                    "firstName": "H. J. T.",
                    "lastName": "Ward"
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                {
                    "creatorType": "author",
                    "firstName": "D.",
                    "lastName": "Everington"
                },
                {
                    "creatorType": "author",
                    "firstName": "E. A.",
                    "lastName": "Croes"
                },
                {
                    "creatorType": "author",
                    "firstName": "A.",
                    "lastName": "Alperovitch"
                },
                {
                    "creatorType": "author",
                    "firstName": "N.",
                    "lastName": "Delasnerie-Lauprêtre"
                },
                {
                    "creatorType": "author",
                    "firstName": "I.",
                    "lastName": "Zerr"
                },
                {
                    "creatorType": "author",
                    "firstName": "S.",
                    "lastName": "Poser"
                },
                {
                    "creatorType": "author",
                    "firstName": "C. M.",
                    "lastName": "van Duijn"
                }
            ],
            "abstractNote": "BACKGROUND: The cause of sporadic Creutzfeldt-Jakob disease (CJD) is unknown. Previous studies found a link with a history of surgery but had methodologic  problems. OBJECTIVE: To help elucidate medical and associated risk factors for  sporadic CJD as part of the 1993 to 1995 European Union collaborative studies of  CJD. METHODS: Medical and associated risk factors from 326 patients with sporadic  CJD, taken from population-based studies performed between 1993 and 1995 in  France, Germany, the Netherlands, and the UK, were compared with 326 community  controls recruited by telephone in 2000. RESULTS: A history of surgery was  significantly associated with the risk of sporadic CJD (odds ratio [OR]: 1.8; 95%  CI: 1.2 to 2.6), which was not dependent on the number of surgical procedures,  and was stronger in females (OR: 2.5; 95% CI: 1.5 to 4.0). Gynecologic (OR: 1.5;  95% CI: 1.0 to 2.3) and \"other\" operations (any operation other than neurologic,  eye, ear, gallbladder, gastrointestinal, and gynecologic operations,  tonsillectomy, and appendectomy) (OR: 1.5; 95% CI: 1.1 to 2.1) were associated  with risk of CJD. Tonsillectomy (OR: 0.3; 95% CI: 0.2 to 0.5) and appendectomy  (OR: 0.6; 95% CI: 0.4 to 0.8) were observed less frequently in cases. An  increased risk was also found with a history of ear piercing in females (OR: 1.6;  95% CI: 1.1 to 2.5) and psychiatric visit(s) (OR: 2.6; 95% CI: 1.5 to 4.3).  CONCLUSIONS: These results support the hypothesis that cases of sporadic CJD may  result from hitherto unrecognized surgical contamination events. However, because  of the limits of the study design, the rarity of the disease, and the potential  for bias, the results should be interpreted with caution.",
            "publicationTitle": "Neurology",
            "publisher": "",
            "place": "United States",
            "date": "2002 Aug 27",
            "volume": "59",
            "issue": "4",
            "section": "",
            "partNumber": "",
            "partTitle": "",
            "pages": "543-548",
            "series": "",
            "seriesTitle": "",
            "seriesText": "",
            "journalAbbreviation": "Neurology",
            "DOI": "10.1212/wnl.59.4.543",
            "citationKey": "",
            "url": "",
            "accessDate": "",
            "PMID": "12196646",
            "PMCID": "",
            "ISSN": "0028-3878",
            "archive": "",
            "archiveLocation": "",
            "shortTitle": "",
            "language": "eng",
            "libraryCatalog": "",
            "callNumber": "",
            "rights": "",
            "extra": "",
            "tags": [
                {
                    "tag": "Aged"
                },
                {
                    "tag": "Case-Control Studies"
                },
                {
                    "tag": "Creutzfeldt-Jakob Syndrome/*epidemiology/*etiology"
                },
                {
                    "tag": "Female"
                },
                {
                    "tag": "France/epidemiology"
                },
                {
                    "tag": "Germany/epidemiology"
                },
                {
                    "tag": "Humans"
                },
                {
                    "tag": "Male"
                },
                {
                    "tag": "Middle Aged"
                },
                {
                    "tag": "Netherlands/epidemiology"
                },
                {
                    "tag": "Odds Ratio"
                },
                {
                    "tag": "Registries/statistics & numerical data"
                },
                {
                    "tag": "Risk Assessment"
                },
                {
                    "tag": "Risk Factors"
                },
                {
                    "tag": "Sex Distribution"
                },
                {
                    "tag": "Sex Factors"
                },
                {
                    "tag": "Surgical Procedures, Operative/*adverse effects/statistics & numerical data"
                },
                {
                    "tag": "United Kingdom/epidemiology"
                }
            ],
            "collections": [
                "344H8INJ"
            ],
            "relations": {},
            "dateAdded": "2026-07-09T16:28:02Z",
            "dateModified": "2026-07-09T16:28:02Z"
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    },
    {
        "key": "33JNYH6E",
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        },
        "meta": {
            "creatorSummary": "Cousens et al.",
            "parsedDate": "1990-06",
            "numChildren": 0
        },
        "data": {
            "key": "33JNYH6E",
            "version": 206430,
            "itemType": "journalArticle",
            "title": "Geographical distribution of cases of Creutzfeldt-Jakob disease in England and Wales 1970-84.",
            "creators": [
                {
                    "creatorType": "author",
                    "firstName": "S. N.",
                    "lastName": "Cousens"
                },
                {
                    "creatorType": "author",
                    "firstName": "R.",
                    "lastName": "Harries-Jones"
                },
                {
                    "creatorType": "author",
                    "firstName": "R.",
                    "lastName": "Knight"
                },
                {
                    "creatorType": "author",
                    "firstName": "R. G.",
                    "lastName": "Will"
                },
                {
                    "creatorType": "author",
                    "firstName": "P. G.",
                    "lastName": "Smith"
                },
                {
                    "creatorType": "author",
                    "firstName": "W. B.",
                    "lastName": "Matthews"
                }
            ],
            "abstractNote": "Two hundred and sixty seven patients with a definite or probable diagnosis of Creutzfeldt-Jakob disease (CJD) were identified in an attempt to ascertain all  cases of the disease in England and Wales in the period 1970-84. No evidence of  space-time clustering of dates and places of onset was found for these cases. Two  age- and sex-matched controls were selected for 72 of the 122 cases diagnosed in  the period 1980-84 and life histories of places of residence were obtained for  these cases and the controls. No evidence was found that cases had lived closer  to each other than had controls at any time in their lives, except that there was  an excess of cases born in London. The study does not provide supportive evidence  for case-to-case transmission of CJD being an important component in the  aetiology of the disease.",
            "publicationTitle": "Journal of neurology, neurosurgery, and psychiatry",
            "publisher": "",
            "place": "England",
            "date": "1990 Jun",
            "volume": "53",
            "issue": "6",
            "section": "",
            "partNumber": "",
            "partTitle": "",
            "pages": "459-465",
            "series": "",
            "seriesTitle": "",
            "seriesText": "",
            "journalAbbreviation": "J Neurol Neurosurg Psychiatry",
            "DOI": "10.1136/jnnp.53.6.459",
            "citationKey": "",
            "url": "",
            "accessDate": "",
            "PMID": "2199610",
            "PMCID": "PMC1014203",
            "ISSN": "0022-3050 1468-330X",
            "archive": "",
            "archiveLocation": "",
            "shortTitle": "",
            "language": "eng",
            "libraryCatalog": "",
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            "tags": [
                {
                    "tag": "Adult"
                },
                {
                    "tag": "Aged"
                },
                {
                    "tag": "Case-Control Studies"
                },
                {
                    "tag": "Creutzfeldt-Jakob Syndrome/*epidemiology/transmission"
                },
                {
                    "tag": "Cross-Sectional Studies"
                },
                {
                    "tag": "England/epidemiology"
                },
                {
                    "tag": "Female"
                },
                {
                    "tag": "Humans"
                },
                {
                    "tag": "Incidence"
                },
                {
                    "tag": "Male"
                },
                {
                    "tag": "Middle Aged"
                },
                {
                    "tag": "Retrospective Studies"
                },
                {
                    "tag": "Risk Factors"
                },
                {
                    "tag": "Wales/epidemiology"
                }
            ],
            "collections": [
                "344H8INJ"
            ],
            "relations": {},
            "dateAdded": "2026-07-09T16:28:02Z",
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    },
    {
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            "creatorSummary": "Nakatani et al.",
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            "version": 206429,
            "itemType": "journalArticle",
            "title": "Temporal and regional variations in sporadic Creutzfeldt-Jakob disease in Japan, 2001-2010.",
            "creators": [
                {
                    "creatorType": "author",
                    "firstName": "E.",
                    "lastName": "Nakatani"
                },
                {
                    "creatorType": "author",
                    "firstName": "T.",
                    "lastName": "Nishimura"
                },
                {
                    "creatorType": "author",
                    "firstName": "B.",
                    "lastName": "Zhou"
                },
                {
                    "creatorType": "author",
                    "firstName": "H.",
                    "lastName": "Kaneda"
                },
                {
                    "creatorType": "author",
                    "firstName": "S.",
                    "lastName": "Teramukai"
                },
                {
                    "creatorType": "author",
                    "firstName": "Y.",
                    "lastName": "Nagai"
                },
                {
                    "creatorType": "author",
                    "firstName": "M.",
                    "lastName": "Fukushima"
                },
                {
                    "creatorType": "author",
                    "firstName": "Y.",
                    "lastName": "Kanatani"
                }
            ],
            "abstractNote": "The objective of this study was to examine temporal and regional variations of sporadic Creutzfeldt-Jakob disease (sCJD) in a retrospective study using Japanese  national surveillance data from 2001 to 2010. We calculated the incidence of sCJD  by age and sex, derived the standardized incidence in each of the 47 prefectures,  and performed spatial disease clustering analysis. The average annual incidence  of sCJD was 1.026 per million in men (637 patients) and 1.132 per million in  women (733 patients), a significant sex difference after adjustment for age (P =  0.001). The ratios of familial CJD to sCJD apparently increased between 2001-2005  and 2006-2010, possibly as a result of the nationwide introduction of genetic  testing after 2006. Based on the data of 2006-2010, certain geographical clusters  of sCJD were identified. The incidence of sCJD was higher in several specific  prefectures compared to the national average. Thus, sCJD appears to have regional  variations, suggesting the existence of genetic or region-specific factors  affecting the incidence of the disease.",
            "publicationTitle": "Epidemiology and infection",
            "publisher": "",
            "place": "England",
            "date": "2015 Apr",
            "volume": "143",
            "issue": "5",
            "section": "",
            "partNumber": "",
            "partTitle": "",
            "pages": "1073-1078",
            "series": "",
            "seriesTitle": "",
            "seriesText": "",
            "journalAbbreviation": "Epidemiol Infect",
            "DOI": "10.1017/S0950268814001605",
            "citationKey": "",
            "url": "",
            "accessDate": "",
            "PMID": "25034354",
            "PMCID": "PMC9507112",
            "ISSN": "1469-4409 0950-2688",
            "archive": "",
            "archiveLocation": "",
            "shortTitle": "",
            "language": "eng",
            "libraryCatalog": "",
            "callNumber": "",
            "rights": "",
            "extra": "",
            "tags": [
                {
                    "tag": "Adolescent"
                },
                {
                    "tag": "Adult"
                },
                {
                    "tag": "Age Distribution"
                },
                {
                    "tag": "Aged"
                },
                {
                    "tag": "Child"
                },
                {
                    "tag": "Child, Preschool"
                },
                {
                    "tag": "Creutzfeldt-Jakob Syndrome/*epidemiology"
                },
                {
                    "tag": "Female"
                },
                {
                    "tag": "Humans"
                },
                {
                    "tag": "Incidence"
                },
                {
                    "tag": "Infant"
                },
                {
                    "tag": "Infant, Newborn"
                },
                {
                    "tag": "Japan/epidemiology"
                },
                {
                    "tag": "Male"
                },
                {
                    "tag": "Middle Aged"
                },
                {
                    "tag": "Retrospective Studies"
                },
                {
                    "tag": "Sex Distribution"
                },
                {
                    "tag": "Time Factors"
                },
                {
                    "tag": "Young Adult"
                },
                {
                    "tag": "spatial modelling"
                }
            ],
            "collections": [
                "344H8INJ"
            ],
            "relations": {},
            "dateAdded": "2026-07-09T16:28:02Z",
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    },
    {
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        "library": {
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        },
        "meta": {
            "creatorSummary": "Cathala et al.",
            "parsedDate": "1986-02-22",
            "numChildren": 0
        },
        "data": {
            "key": "TU5BC2B8",
            "version": 206428,
            "itemType": "journalArticle",
            "title": "[Creutzfeldt-Jakob disease in France. Value of familial forms. Is there a gene controlling the length of the incubation period?].",
            "creators": [
                {
                    "creatorType": "author",
                    "firstName": "F.",
                    "lastName": "Cathala"
                },
                {
                    "creatorType": "author",
                    "firstName": "P.",
                    "lastName": "Brown"
                },
                {
                    "creatorType": "author",
                    "firstName": "J.",
                    "lastName": "Chatelain"
                },
                {
                    "creatorType": "author",
                    "firstName": "P.",
                    "lastName": "Castaigne"
                },
                {
                    "creatorType": "author",
                    "firstName": "C.",
                    "lastName": "Gajdusek"
                }
            ],
            "abstractNote": "An extensive search for patients who died of Creutzfeld-Jakob disease in France between 1968 and 1982 resulted in the discovery of 327 cases, 233 of which were  histologically proven and 29 transmitted to animals; 17 patients belonged to 6  families. Further investigations among members of these 6 families yielded 21  additional cases, i.e. a total of 38 familial cases. Studies among sibships  suggested an autosomal dominant pattern of transmission but did not exclude  lateral contamination infancy. The patients' age at death was 10 to 15 years  lower than that of the total of French cases and seemed to be a characteristic of  each individual family. This suggests that, as in scrapie, a gene may control the  length of the incubation period.",
            "publicationTitle": "Presse medicale (Paris, France : 1983)",
            "publisher": "",
            "place": "France",
            "date": "1986 Feb 22",
            "volume": "15",
            "issue": "8",
            "section": "",
            "partNumber": "",
            "partTitle": "",
            "pages": "379-382",
            "series": "",
            "seriesTitle": "",
            "seriesText": "",
            "journalAbbreviation": "Presse Med",
            "DOI": "",
            "citationKey": "",
            "url": "",
            "accessDate": "",
            "PMID": "2938156",
            "PMCID": "",
            "ISSN": "0755-4982",
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            "archiveLocation": "",
            "shortTitle": "",
            "language": "fre",
            "libraryCatalog": "",
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            "tags": [
                {
                    "tag": "Adult"
                },
                {
                    "tag": "Aged"
                },
                {
                    "tag": "Animals"
                },
                {
                    "tag": "Creutzfeldt-Jakob Syndrome/epidemiology/*genetics/transmission"
                },
                {
                    "tag": "Female"
                },
                {
                    "tag": "France"
                },
                {
                    "tag": "Genes"
                },
                {
                    "tag": "Humans"
                },
                {
                    "tag": "Male"
                },
                {
                    "tag": "Middle Aged"
                },
                {
                    "tag": "Time Factors"
                }
            ],
            "collections": [
                "344H8INJ"
            ],
            "relations": {},
            "dateAdded": "2026-07-09T16:28:02Z",
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    {
        "key": "DUBQET2H",
        "version": 206427,
        "library": {
            "type": "user",
            "id": 6212901,
            "name": "Nick Petosky",
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        },
        "meta": {
            "creatorSummary": "Mitrová",
            "parsedDate": "1991-09",
            "numChildren": 0
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        "data": {
            "key": "DUBQET2H",
            "version": 206427,
            "itemType": "journalArticle",
            "title": "Some new aspects of CJD epidemiology in Slovakia.",
            "creators": [
                {
                    "creatorType": "author",
                    "firstName": "E.",
                    "lastName": "Mitrová"
                }
            ],
            "abstractNote": "Descriptive epidemiological and genealogical data obtained by prospective and retrospective studies on CJD in Slovakia and in patients emigrating from CJD  clusters were analysed. Observations contradictory to an exclusively genetic  etiology of temporo-spatial accumulation of CJD are presented. Data indicating a  genetically increased susceptibility to the disease and its coincidence with  environmental risk in clustering patients are discussed.",
            "publicationTitle": "European journal of epidemiology",
            "publisher": "",
            "place": "Netherlands",
            "date": "1991 Sep",
            "volume": "7",
            "issue": "5",
            "section": "",
            "partNumber": "",
            "partTitle": "",
            "pages": "439-449",
            "series": "",
            "seriesTitle": "",
            "seriesText": "",
            "journalAbbreviation": "Eur J Epidemiol",
            "DOI": "10.1007/BF00143119",
            "citationKey": "",
            "url": "",
            "accessDate": "",
            "PMID": "1761100",
            "PMCID": "",
            "ISSN": "0393-2990",
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            "shortTitle": "",
            "language": "eng",
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                    "tag": "Creutzfeldt-Jakob Syndrome/*epidemiology/genetics"
                },
                {
                    "tag": "Czechoslovakia/epidemiology"
                },
                {
                    "tag": "Disease Susceptibility"
                },
                {
                    "tag": "Female"
                },
                {
                    "tag": "Humans"
                },
                {
                    "tag": "Male"
                },
                {
                    "tag": "Middle Aged"
                },
                {
                    "tag": "Pedigree"
                },
                {
                    "tag": "Prospective Studies"
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                {
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