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Items: 1 to 20 of 77

1.

Health professions and risk of sporadic Creutzfeldt-Jakob disease, 1965 to 2010.

Alcalde-Cabero E, Almazan-Isla J, Brandel JP, Breithaupt M, Catarino J, Collins S, Hayback J, Hoftberger R, Kahana E, Kovacs GG, Ladogana A, Mitrova E, Molesworth A, Nakamura Y, Pocchiari M, Popovic M, Ruiz-Tovar M, Taratuto A, van Duijn C, Yamada M, Will RG, Zerr I, de Pedro Cuesta J.

Euro Surveill. 2012 Apr 12;17(15). pii: 20144. Review.

2.

Occupational risk factors for the sporadic form of Creutzfeldt-Jakob disease.

Cocco PL, Caperna A, Vinci F.

Med Lav. 2003 Jul-Aug;94(4):353-63.

PMID:
14526494
3.

Surgery and risk of sporadic Creutzfeldt-Jakob disease in Denmark and Sweden: registry-based case-control studies.

Mahillo-Fernandez I, de Pedro-Cuesta J, Bleda MJ, Cruz M, Mølbak K, Laursen H, Falkenhorst G, Martínez-Martín P, Siden A; EUROSURGYCJD Research Group.

Neuroepidemiology. 2008;31(4):229-40. doi: 10.1159/000163097. Epub 2008 Oct 9.

4.

Nosocomial transmission of sporadic Creutzfeldt-Jakob disease: results from a risk-based assessment of surgical interventions.

de Pedro-Cuesta J, Mahillo-Fernández I, Rábano A, Calero M, Cruz M, Siden A, Laursen H, Falkenhorst G, Mølbak K; EUROSURGYCJD Research Group.

J Neurol Neurosurg Psychiatry. 2011 Feb;82(2):204-12. doi: 10.1136/jnnp.2009.188425. Epub 2010 Jun 14.

5.

A case-control study of sporadic Creutzfeldt-Jakob disease in Switzerland: analysis of potential risk factors with regard to an increased CJD incidence in the years 2001-2004.

Ruegger J, Stoeck K, Amsler L, Blaettler T, Zwahlen M, Aguzzi A, Glatzel M, Hess K, Eckert T.

BMC Public Health. 2009 Jan 14;9:18. doi: 10.1186/1471-2458-9-18.

6.

Medical procedures and risk for sporadic Creutzfeldt-Jakob disease, Japan, 1999-2008.

Hamaguchi T, Noguchi-Shinohara M, Nozaki I, Nakamura Y, Sato T, Kitamoto T, Mizusawa H, Yamada M.

Emerg Infect Dis. 2009 Feb;15(2):265-71.

7.

Tissue classification for the epidemiological assessment of surgical transmission of sporadic Creutzfeldt-Jakob disease. A proposal on hypothetical risk levels.

Rábano A, de Pedro-Cuesta J, Mølbak K, Siden A, Calero M, Laursen H; EUROSURGYCJD Research Group.

BMC Public Health. 2005 Jan 24;5:9.

8.

The risk of iatrogenic Creutzfeldt-Jakob disease through medical and surgical procedures.

Hamaguchi T, Noguchi-Shinohara M, Nozaki I, Nakamura Y, Sato T, Kitamoto T, Mizusawa H, Yamada M.

Neuropathology. 2009 Oct;29(5):625-31. doi: 10.1111/j.1440-1789.2009.01023.x. Epub 2009 Jul 29. Review.

PMID:
19659942
9.

Quantification of surviving cerebellar granule neurones and abnormal prion protein (PrPSc) deposition in sporadic Creutzfeldt-Jakob disease supports a pathogenic role for small PrPSc deposits common to the various molecular subtypes.

Faucheux BA, Morain E, Diouron V, Brandel JP, Salomon D, Sazdovitch V, Privat N, Laplanche JL, Hauw JJ, Haïk S.

Neuropathol Appl Neurobiol. 2011 Aug;37(5):500-12. doi: 10.1111/j.1365-2990.2011.01179.x.

PMID:
21450052
10.

Preclinical sporadic Creutzfeldt-Jakob disease in French blood donors: an epidemiologic model-based study.

Pillonel J, Brandel JP, Léon L, Salomon D, Haïk S, Capek I, Vaillant V, Coste J, Alpérovitch A.

Transfusion. 2012 Jun;52(6):1290-5. doi: 10.1111/j.1537-2995.2011.03459.x. Epub 2011 Dec 1.

PMID:
22128904
11.

Creutzfeldt-Jakob disease in Slovenia from 1985 to 2003.

Popović M, Glavac D, Smerkolj S, Svigelj V, Kalan G, Galvani V, Cernilec M, Bresjanac M.

Wien Klin Wochenschr. 2004 Aug 31;116(15-16):524-9.

PMID:
15471179
12.
13.

Creutzfeldt-Jakob disease in Ireland: epidemiological aspects 1980-2002.

Horan G, Keohane C, Molloy S, Howley R, Harney M, Heffernan J, McGuigan C, Hutchinson M, Brett F, Farrell M.

Eur Neurol. 2004;51(3):132-7. Epub 2004 Feb 26.

PMID:
14988606
14.

Creutzfeldt-Jakob disease surveillance in Argentina, 1997-2008.

Begué C, Martinetto H, Schultz M, Rojas E, Romero C, D'Giano C, Sevlever G, Somoza M, Taratuto AL.

Neuroepidemiology. 2011;37(3-4):193-202. doi: 10.1159/000331907. Epub 2011 Nov 5.

PMID:
22067221
15.

Classification of surgical procedures for epidemiologic assessment of sporadic Creutzfeldt-Jakob disease transmission by surgery.

de Pedro-Cuesta J, Bleda MJ, Rábano A, Cruz M, Laursen H, Mølbak K, Siden A.

Eur J Epidemiol. 2006;21(8):595-604. Epub 2006 Sep 20.

PMID:
17031517
16.

Prospective 10-year surveillance of human prion diseases in Japan.

Nozaki I, Hamaguchi T, Sanjo N, Noguchi-Shinohara M, Sakai K, Nakamura Y, Sato T, Kitamoto T, Mizusawa H, Moriwaka F, Shiga Y, Kuroiwa Y, Nishizawa M, Kuzuhara S, Inuzuka T, Takeda M, Kuroda S, Abe K, Murai H, Murayama S, Tateishi J, Takumi I, Shirabe S, Harada M, Sadakane A, Yamada M.

Brain. 2010 Oct;133(10):3043-57. doi: 10.1093/brain/awq216. Epub 2010 Sep 20.

PMID:
20855418
17.

Geographical analysis of the sporadic Creutzfeldt-Jakob disease distribution in the autonomous community of the Basque Country for the period 1995-2008.

Chamosa S, Tamayo I, Arteagoitia-Axpe JM, Juste RA, Rodríguez-Martínez AB, Zarranz-Imirizaldu JJ, Arriola L.

Eur Neurol. 2014;72(1-2):20-5. doi: 10.1159/000358298. Epub 2014 May 8.

PMID:
24819667
18.

Diagnostic profiles of patients with late-onset Creutzfeldt-Jakob disease differ from those of younger Creutzfeldt-Jakob patients: a historical cohort study using data from the German National Reference Center.

Karch A, Raddatz LM, Ponto C, Hermann P, Summers D, Zerr I.

J Neurol. 2014 May;261(5):877-83. doi: 10.1007/s00415-014-7283-1. Epub 2014 Feb 26.

PMID:
24570280
19.

Enhanced geographically restricted surveillance simulates sporadic Creutzfeldt-Jakob disease cluster.

Klug GM, Wand H, Boyd A, Law M, Whyte S, Kaldor J, Masters CL, Collins S.

Brain. 2009 Feb;132(Pt 2):493-501. doi: 10.1093/brain/awn303. Epub 2008 Nov 28.

PMID:
19042933
20.

Analysis of prion strains by PrPSc profiling in sporadic Creutzfeldt-Jakob disease.

Schoch G, Seeger H, Bogousslavsky J, Tolnay M, Janzer RC, Aguzzi A, Glatzel M.

PLoS Med. 2006 Feb;3(2):e14. Epub 2005 Dec 20.

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