Νόσος Κρόιτσφελντ-Γιάκομπ (Greek Wikipedia)

Analysis of information sources in references of the Wikipedia article "Νόσος Κρόιτσφελντ-Γιάκομπ" in Greek language version.

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ajnr.org

«Diffusion-weighted and fluid-attenuated inversion recovery imaging in Creutzfeldt-Jakob disease: high sensitivity and specificity for diagnosis». AJNR. American Journal of Neuroradiology 26 (6): 1551–62. June–July 2005. PMID 15956529. Αρχειοθετήθηκε από το πρωτότυπο στις 2008-09-07. https://web.archive.org/web/20080907152111/http://www.ajnr.org/cgi/content/full/26/6/1551.
«Thalamic involvement in sporadic Creutzfeldt-Jakob disease: a diffusion-weighted MR imaging study». AJNR. American Journal of Neuroradiology 24 (5): 908–15. May 2003. PMID 12748093. Αρχειοθετήθηκε από το πρωτότυπο στις 10 October 2008. https://web.archive.org/web/20081010214648/http://www.ajnr.org/cgi/content/full/24/5/908.

archive.org

«Creutzfeldt-Jakob disease: clinical analysis of a consecutive series of 230 neuropathologically verified cases». Annals of Neurology 20 (5): 597–602. November 1986. doi:10.1002/ana.410200507. PMID 3539001. https://archive.org/details/sim_annals-of-neurology_1986-11_20_5/page/597.
«Transmissible and non-transmissible neurodegenerative disease: similarities in age of onset and genetics in relation to aetiology». Psychological Medicine 16 (1): 199–207. February 1986. doi:10.1017/s0033291700002634. PMID 3961045. https://archive.org/details/sim_psychological-medicine_1986-02_16_1/page/199.
«Descriptive epidemiology of Creutzfeldt-Jakob disease in six European countries, 1993-1995. EU Collaborative Study Group for CJD». Annals of Neurology 43 (6): 763–7. June 1998. doi:10.1002/ana.410430611. PMID 9629846. https://archive.org/details/sim_annals-of-neurology_1998-06_43_6/page/763.
«Creutzfeldt-Jakob disease and lyophilised dura mater grafts: report of two cases». Journal of Neurology, Neurosurgery, and Psychiatry 56 (9): 999–1000. September 1993. doi:10.1136/jnnp.56.9.999. PMID 8410042. PMC 489736. https://archive.org/details/sim_journal-of-neurology-neurosurgery-and-psychiatry_1993-09_56_9/page/999.
Sattar, Hussain A. (2011). Fundamentals of Pathology. Chicago: Pathoma LLC. σελ. 187.
«Treatable neurological disorders misdiagnosed as Creutzfeldt-Jakob disease». Annals of Neurology 70 (3): 437–44. September 2011. doi:10.1002/ana.22454. PMID 21674591. PMC 3170496. https://archive.org/details/sim_annals-of-neurology_2011-09_70_3/page/437.
«MR imaging of Creutzfeldt-Jakob disease». Radiology 199 (3): 793–8. June 1996. doi:10.1148/radiology.199.3.8638007. PMID 8638007. https://archive.org/details/sim_radiology_1996-06_199_3/page/793.
«Serial diffusion-weighted MRI of Creutzfeldt-Jakob disease». AJR. American Journal of Roentgenology 184 (2): 560–6. February 2005. doi:10.2214/ajr.184.2.01840560. PMID 15671380. https://archive.org/details/sim_ajr-american-journal-of-roentgenology_2005-02_184_2/page/560.
«Variant Creutzfeldt-Jakob disease and bovine spongiform encephalopathy». Clinics in Laboratory Medicine 22 (4): 849–62, v-vi. December 2002. doi:10.1016/S0272-2712(02)00024-0. PMID 12489284. https://archive.org/details/sim_clinics-in-laboratory-medicine_2002-12_22_4/page/849.
«Panencephalopathic type of Creutzfeldt-Jakob disease: primary involvement of the cerebral white matter». Journal of Neurology, Neurosurgery, and Psychiatry 44 (2): 103–15. February 1981. doi:10.1136/jnnp.44.2.103. PMID 7012278. PMC 490840. https://archive.org/details/sim_journal-of-neurology-neurosurgery-and-psychiatry_1981-02_44_2/page/103.
«Sporadic and familial CJD: classification and characterisation». British Medical Bulletin 66: 213–39. 2003. doi:10.1093/bmb/66.1.213. PMID 14522861. https://archive.org/details/sim_british-medical-bulletin_2003_66/page/213.

books.google.com

Sattar, Husain A. (2017). Fundamentals of Pathology. σελ. 189. ISBN 9780983224631.

cdc.gov

«Creutzfeldt-Jakob Disease, Classic (CJD)». CDC. 2 Οκτωβρίου 2018. Ανακτήθηκε στις 21 Νοεμβρίου 2018.
«Creutzfeldt-Jakob Disease, Classic (CJD) | Prion Diseases | CDC». www.cdc.gov (στα Αγγλικά). 1 Φεβρουαρίου 2019. Ανακτήθηκε στις 17 Ιουνίου 2019. Classic CJD is a human prion disease
«About CJD | Creutzfeldt–Jakob Disease, Classic (CJD) | Prion Disease». CDC. 11 Φεβρουαρίου 2015. Αρχειοθετήθηκε από το πρωτότυπο στις 8 Αυγούστου 2017. Ανακτήθηκε στις 16 Ιουλίου 2017.
«Creutzfeldt–Jakob Disease, Classic (CJD) | Prion Diseases». CDC. 6 Φεβρουαρίου 2015. Αρχειοθετήθηκε από το πρωτότυπο στις 18 Ιουλίου 2017. Ανακτήθηκε στις 16 Ιουλίου 2017.
«Questions and Answers: Creutzfeldt–Jakob Disease Infection-Control Practices». Infection Control Practices/CJD (Creutzfeldt–Jakob Disease, Classic). Centers for Disease Control and Prevention. 4 Ιανουαρίου 2007. Αρχειοθετήθηκε από το πρωτότυπο στις 17 Οκτωβρίου 2007. Ανακτήθηκε στις 9 Ιουνίου 2007.
«vCJD (Variant Creutzfeldt–Jakob Disease)». Centers for Disease Control and Prevention. 4 Ιανουαρίου 2007. Αρχειοθετήθηκε από το πρωτότυπο στις 7 Μαΐου 2009. Ανακτήθηκε στις 20 Ιουνίου 2009.
«CJD (Creutzfeldt–Jakob Disease, Classic)». Centers for Disease Control and Prevention. 26 Φεβρουαρίου 2008. Αρχειοθετήθηκε από το πρωτότυπο στις 6 Μαΐου 2009. Ανακτήθηκε στις 20 Ιουνίου 2009.
"Occurrence and Transmission | Creutzfeldt-Jakob Disease, Classic (CJD) | Prion Disease | CDC". www.cdc.gov. 2019-05-08. Retrieved 2020-11-04.

clinicalkey.com

Uttley L, Carroll C, Wong R, Hilton DA, Stevenson M. Creutzfeldt-Jakob disease: a systematic review of global incidence, prevalence, infectivity, and incubation. Lancet Infect Dis. 2020 Jan;20(1):e2-e10. doi: 10.1016/S1473-3099(19)30615-2. PMID 31876504
Bosque, Patrick· Tyler, Kenneth (2020). Prions and Prion Disease of the Central Nervous System (Transmissible Neurodegenerative Diseases). www.clinicalkey.com: Elsevier, Inc. σελίδες 2288–2300.

doi.org

dx.doi.org

Manix, Marc; Kalakoti, Piyush; Henry, Miriam; Thakur, Jai; Menger, Richard; Guthikonda, Bharat; Nanda, Anil (2015-11-01). «Creutzfeldt-Jakob disease: updated diagnostic criteria, treatment algorithm, and the utility of brain biopsy» (στα αγγλικά). Neurosurgical Focus 39 (5): E2. doi:10.3171/2015.8.FOCUS15328. ISSN 1092-0684. PMID 26646926.
«Creutzfeldt-Jakob disease: clinical analysis of a consecutive series of 230 neuropathologically verified cases». Annals of Neurology 20 (5): 597–602. November 1986. doi:10.1002/ana.410200507. PMID 3539001. https://archive.org/details/sim_annals-of-neurology_1986-11_20_5/page/597.
Atalay, Fatma Oz; Tolunay, Sahsine; Ozgun, Gonca; Bekar, Ahmet; Zarifoglu, Mehmet (2013). «Creutzfeldt-jakob disease: report of four cases and review of the literature». Turkish Journal of Pathology. doi:10.5146/tjpath.2013.01195. ISSN 1018-5615. PMID 24272930. http://www.turkjpath.org/text.php3?doi=10.5146/tjpath.2013.01195.
«The molecular biology of prion propagation». Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences 356 (1406): 185–95. February 2001. doi:10.1098/rstb.2000.0764. PMID 11260799.
«Transmissible and non-transmissible neurodegenerative disease: similarities in age of onset and genetics in relation to aetiology». Psychological Medicine 16 (1): 199–207. February 1986. doi:10.1017/s0033291700002634. PMID 3961045. https://archive.org/details/sim_psychological-medicine_1986-02_16_1/page/199.
«Descriptive epidemiology of Creutzfeldt-Jakob disease in six European countries, 1993-1995. EU Collaborative Study Group for CJD». Annals of Neurology 43 (6): 763–7. June 1998. doi:10.1002/ana.410430611. PMID 9629846. https://archive.org/details/sim_annals-of-neurology_1998-06_43_6/page/763.
«Risk of Creutzfeldt-Jakob disease transmission by ocular surgery and tissue transplantation». Eye 23 (10): 1926–30. October 2009. doi:10.1038/eye.2008.381. PMID 19136921.
«Creutzfeldt-Jakob disease and lyophilised dura mater grafts: report of two cases». Journal of Neurology, Neurosurgery, and Psychiatry 56 (9): 999–1000. September 1993. doi:10.1136/jnnp.56.9.999. PMID 8410042. PMC 489736. https://archive.org/details/sim_journal-of-neurology-neurosurgery-and-psychiatry_1993-09_56_9/page/999.
«Danger of accidental person-to-person transmission of Creutzfeldt-Jakob disease by surgery». Lancet 1 (8009): 478–9. February 1977. doi:10.1016/s0140-6736(77)91958-4. PMID 65575.
«Iatrogenic Creutzfeldt-Jakob disease, final assessment». Emerging Infectious Diseases 18 (6): 901–7. June 2012. doi:10.3201/eid1806.120116. PMID 22607808.
«Human spongiform encephalopathy: the National Institutes of Health series of 300 cases of experimentally transmitted disease». Annals of Neurology 35 (5): 513–29. May 1994. doi:10.1002/ana.410350504. PMID 8179297.
«Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD». Nature 383 (6602): 685–90. October 1996. doi:10.1038/383685a0. PMID 8878476. Bibcode: 1996Natur.383..685C.
«Kuru in the 21st century--an acquired human prion disease with very long incubation periods». Lancet 367 (9528): 2068–74. June 2006. doi:10.1016/s0140-6736(06)68930-7. PMID 16798390.
«The challenge of prion decontamination». Clinical Infectious Diseases 36 (9): 1152–4. May 2003. doi:10.1086/374668. PMID 12715310.
«A novel copper-hydrogen peroxide formulation for prion decontamination». The Journal of Infectious Diseases 194 (6): 865–9. September 2006. doi:10.1086/506947. PMID 16941355.
«An enzyme-detergent method for effective prion decontamination of surgical steel». The Journal of General Virology 86 (Pt 3): 869–78. March 2005. doi:10.1099/vir.0.80484-0. PMID 15722550.
«CJD mimics and chameleons». Practical Neurology 17 (2): 113–121. April 2017. doi:10.1136/practneurol-2016-001571. PMID 28153848.
«The 14-3-3 protein detectable in the cerebrospinal fluid of patients with prion-unrelated neurological diseases is expressed constitutively in neurons and glial cells in culture». European Neurology 41 (4): 216–25. 1999. doi:10.1159/000008054. PMID 10343153.
«Challenging the clinical utility of the 14-3-3 protein for the diagnosis of sporadic Creutzfeldt-Jakob disease». Archives of Neurology 60 (6): 813–6. June 2003. doi:10.1001/archneur.60.6.813. PMID 12810484.
«Treatable neurological disorders misdiagnosed as Creutzfeldt-Jakob disease». Annals of Neurology 70 (3): 437–44. September 2011. doi:10.1002/ana.22454. PMID 21674591. PMC 3170496. https://archive.org/details/sim_annals-of-neurology_2011-09_70_3/page/437.
«Early detection of abnormal prion protein in genetic human prion diseases now possible using real-time QUIC assay». PLOS ONE 8 (1): e54915. 2013-01-25. doi:10.1371/journal.pone.0054915. PMID 23372790. Bibcode: 2013PLoSO...854915S.
«Diagnostic and prognostic value of human prion detection in cerebrospinal fluid». Annals of Neurology 81 (1): 79–92. January 2017. doi:10.1002/ana.24833. PMID 27893164.
«Diagnosis of Human Prion Disease Using Real-Time Quaking-Induced Conversion Testing of Olfactory Mucosa and Cerebrospinal Fluid Samples». JAMA Neurology 74 (2): 155–162. February 2017. doi:10.1001/jamaneurol.2016.4614. PMID 27942718.
«CSF tests in the differential diagnosis of Creutzfeldt-Jakob disease». Neurology 67 (4): 637–43. August 2006. doi:10.1212/01.wnl.0000230159.67128.00. PMID 16924018.
«A highly sensitive immunoassay for the detection of prion-infected material in whole human blood without the use of proteinase K». Transfusion 50 (12): 2619–27. December 2010. doi:10.1111/j.1537-2995.2010.02731.x. PMID 20561299. http://discovery.ucl.ac.uk/146121/1/Tattum_et_al_A_highly_sensitive_immunoassay_for_the_detection_of_prion_infected_ELISA.pdf.
«Imaging of Creutzfeldt-Jakob Disease: Imaging Patterns and Their Differential Diagnosis». Radiographics 37 (1): 234–257. 2017-01-01. doi:10.1148/rg.2017160075. PMID 28076012.
«MR imaging of Creutzfeldt-Jakob disease». Radiology 199 (3): 793–8. June 1996. doi:10.1148/radiology.199.3.8638007. PMID 8638007. https://archive.org/details/sim_radiology_1996-06_199_3/page/793.
«Serial diffusion-weighted MRI of Creutzfeldt-Jakob disease». AJR. American Journal of Roentgenology 184 (2): 560–6. February 2005. doi:10.2214/ajr.184.2.01840560. PMID 15671380. https://archive.org/details/sim_ajr-american-journal-of-roentgenology_2005-02_184_2/page/560.
«An ominous radiographic feature: cortical ribbon sign». Internal and Emergency Medicine 11 (2): 281–3. March 2016. doi:10.1007/s11739-015-1287-4. PMID 26238299.
«The end of the BSE saga: do we still need surveillance for human prion diseases?». Swiss Medical Weekly 145: w14212. 12 November 2015. doi:10.4414/smw.2015.14212. PMID 26715203. http://www.zora.uzh.ch/id/eprint/115870/1/smw-2015-14212.pdf.
«Human prion diseases: surgical lessons learned from iatrogenic prion transmission». Neurosurgical Focus 41 (1): E10. July 2016. doi:10.3171/2016.5.FOCUS15126. PMID 27364252.
«Variant Creutzfeldt-Jakob disease and bovine spongiform encephalopathy». Clinics in Laboratory Medicine 22 (4): 849–62, v-vi. December 2002. doi:10.1016/S0272-2712(02)00024-0. PMID 12489284. https://archive.org/details/sim_clinics-in-laboratory-medicine_2002-12_22_4/page/849.
«Creutzfeldt-Jakob disease: updated diagnostic criteria, treatment algorithm, and the utility of brain biopsy». Neurosurgical Focus 39 (5): E2. November 2015. doi:10.3171/2015.8.FOCUS15328. PMID 26646926.
«Treating seizures in Creutzfeldt-Jakob disease». Epilepsy & Behavior Case Reports 2: 75–9. 2014-02-07. doi:10.1016/j.ebcr.2014.01.004. PMID 25667875.
«Panencephalopathic type of Creutzfeldt-Jakob disease: primary involvement of the cerebral white matter». Journal of Neurology, Neurosurgery, and Psychiatry 44 (2): 103–15. February 1981. doi:10.1136/jnnp.44.2.103. PMID 7012278. PMC 490840. https://archive.org/details/sim_journal-of-neurology-neurosurgery-and-psychiatry_1981-02_44_2/page/103.
«Klinische und genealogische Beobachtungen bei einem Fall von spastischer Pseudokosklerose Jakobs». Zeitschrift für die Gesamte Neurologie und Psychiatrie 128 (1–4): 337–41. 1930. doi:10.1007/bf02864269.
«Sporadic and familial CJD: classification and characterisation». British Medical Bulletin 66: 213–39. 2003. doi:10.1093/bmb/66.1.213. PMID 14522861. https://archive.org/details/sim_british-medical-bulletin_2003_66/page/213.
«Is Creutzfeldt-Jakob disease transmitted in blood?». Emerging Infectious Diseases 3 (2): 155–63. 1997. doi:10.3201/eid0302.970208. PMID 9204296.
«Update: Dura Mater Graft-Associated Creutzfeldt-Jakob Disease - Japan, 1975-2017». MMWR. Morbidity and Mortality Weekly Report 67 (9): 274–278. March 2018. doi:10.15585/mmwr.mm6709a3. PMID 29518068.
«Cells infected with scrapie and Creutzfeldt-Jakob disease agents produce intracellular 25-nm virus-like particles». Proceedings of the National Academy of Sciences of the United States of America 104 (6): 1965–70. February 2007. doi:10.1073/pnas.0610999104. PMID 17267596. Bibcode: 2007PNAS..104.1965M.

harvard.edu

adsabs.harvard.edu

«Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD». Nature 383 (6602): 685–90. October 1996. doi:10.1038/383685a0. PMID 8878476. Bibcode: 1996Natur.383..685C.
«Early detection of abnormal prion protein in genetic human prion diseases now possible using real-time QUIC assay». PLOS ONE 8 (1): e54915. 2013-01-25. doi:10.1371/journal.pone.0054915. PMID 23372790. Bibcode: 2013PLoSO...854915S.
«Cells infected with scrapie and Creutzfeldt-Jakob disease agents produce intracellular 25-nm virus-like particles». Proceedings of the National Academy of Sciences of the United States of America 104 (6): 1965–70. February 2007. doi:10.1073/pnas.0610999104. PMID 17267596. Bibcode: 2007PNAS..104.1965M.

medscape.com

reference.medscape.com

«A 49-Year-Old Man With Forgetfulness and Gait Impairment». reference.medscape.com/viewarticle/881806_3. Αρχειοθετήθηκε από το πρωτότυπο στις 6 Ιουλίου 2017. Ανακτήθηκε στις 9 Ιουλίου 2017.

merckmanuals.com

Gambetti, Pierluigi. «Creutzfeldt–Jakob Disease (CJD)». The Merck Manuals: Online Medical Library. Αρχειοθετήθηκε από το πρωτότυπο στις 4 Ιουνίου 2011. Ανακτήθηκε στις 4 Ιουνίου 2011.

nhs.uk

«Treatment». nhs.uk. 23 Οκτωβρίου 2017. Ανακτήθηκε στις 17 Απριλίου 2018.

nih.gov

nobelprize.org

«The Nobel Prize in Physiology or Medicine 1997: Stanley B. Prusiner». NobelPrize.org. Αρχειοθετήθηκε από το πρωτότυπο στις 20 Φεβρουαρίου 2011. Ανακτήθηκε στις 21 Φεβρουαρίου 2011.

turkjpath.org

Atalay, Fatma Oz; Tolunay, Sahsine; Ozgun, Gonca; Bekar, Ahmet; Zarifoglu, Mehmet (2013). «Creutzfeldt-jakob disease: report of four cases and review of the literature». Turkish Journal of Pathology. doi:10.5146/tjpath.2013.01195. ISSN 1018-5615. PMID 24272930. http://www.turkjpath.org/text.php3?doi=10.5146/tjpath.2013.01195.

ucl.ac.uk

discovery.ucl.ac.uk

«A highly sensitive immunoassay for the detection of prion-infected material in whole human blood without the use of proteinase K». Transfusion 50 (12): 2619–27. December 2010. doi:10.1111/j.1537-2995.2010.02731.x. PMID 20561299. http://discovery.ucl.ac.uk/146121/1/Tattum_et_al_A_highly_sensitive_immunoassay_for_the_detection_of_prion_infected_ELISA.pdf.

umn.edu

cidrap.umn.edu

New form of BSE resembles sporadic CJD

utah.edu

library.med.utah.edu

«Pathology of Degenerative CNS Diseases». library.med.utah.edu.

uzh.ch

zora.uzh.ch

«The end of the BSE saga: do we still need surveillance for human prion diseases?». Swiss Medical Weekly 145: w14212. 12 November 2015. doi:10.4414/smw.2015.14212. PMID 26715203. http://www.zora.uzh.ch/id/eprint/115870/1/smw-2015-14212.pdf.

web.archive.org

«Creutzfeldt–Jakob Disease Fact Sheet | National Institute of Neurological Disorders and Stroke». NINDS. Μαρτίου 2003. Αρχειοθετήθηκε από το πρωτότυπο στις 4 Ιουλίου 2017. Ανακτήθηκε στις 16 Ιουλίου 2017.
«About CJD | Creutzfeldt–Jakob Disease, Classic (CJD) | Prion Disease». CDC. 11 Φεβρουαρίου 2015. Αρχειοθετήθηκε από το πρωτότυπο στις 8 Αυγούστου 2017. Ανακτήθηκε στις 16 Ιουλίου 2017.
«Creutzfeldt–Jakob Disease, Classic (CJD) | Prion Diseases». CDC. 6 Φεβρουαρίου 2015. Αρχειοθετήθηκε από το πρωτότυπο στις 18 Ιουλίου 2017. Ανακτήθηκε στις 16 Ιουλίου 2017.
«A 49-Year-Old Man With Forgetfulness and Gait Impairment». reference.medscape.com/viewarticle/881806_3. Αρχειοθετήθηκε από το πρωτότυπο στις 6 Ιουλίου 2017. Ανακτήθηκε στις 9 Ιουλίου 2017.
Gambetti, Pierluigi. «Creutzfeldt–Jakob Disease (CJD)». The Merck Manuals: Online Medical Library. Αρχειοθετήθηκε από το πρωτότυπο στις 4 Ιουνίου 2011. Ανακτήθηκε στις 4 Ιουνίου 2011.
«Questions and Answers: Creutzfeldt–Jakob Disease Infection-Control Practices». Infection Control Practices/CJD (Creutzfeldt–Jakob Disease, Classic). Centers for Disease Control and Prevention. 4 Ιανουαρίου 2007. Αρχειοθετήθηκε από το πρωτότυπο στις 17 Οκτωβρίου 2007. Ανακτήθηκε στις 9 Ιουνίου 2007.
«WHO Infection Control Guidelines for Transmissible Spongiform Encephalopathies». World Health Organization: Communicable Disease Surveillance and Control. 26 Μαρτίου 1999. Αρχειοθετήθηκε από το πρωτότυπο στις 18 Μαΐου 2007. Ανακτήθηκε στις 9 Ιουνίου 2007.
«Diffusion-weighted and fluid-attenuated inversion recovery imaging in Creutzfeldt-Jakob disease: high sensitivity and specificity for diagnosis». AJNR. American Journal of Neuroradiology 26 (6): 1551–62. June–July 2005. PMID 15956529. Αρχειοθετήθηκε από το πρωτότυπο στις 2008-09-07. https://web.archive.org/web/20080907152111/http://www.ajnr.org/cgi/content/full/26/6/1551.
«Thalamic involvement in sporadic Creutzfeldt-Jakob disease: a diffusion-weighted MR imaging study». AJNR. American Journal of Neuroradiology 24 (5): 908–15. May 2003. PMID 12748093. Αρχειοθετήθηκε από το πρωτότυπο στις 10 October 2008. https://web.archive.org/web/20081010214648/http://www.ajnr.org/cgi/content/full/24/5/908.
«who.int: "Fact sheets no 180: Variant Creutzfeldt–Jakob disease" Feb 2012 ed». Αρχειοθετήθηκε από το πρωτότυπο στις 4 Φεβρουαρίου 2016.
«vCJD (Variant Creutzfeldt–Jakob Disease)». Centers for Disease Control and Prevention. 4 Ιανουαρίου 2007. Αρχειοθετήθηκε από το πρωτότυπο στις 7 Μαΐου 2009. Ανακτήθηκε στις 20 Ιουνίου 2009.
«CJD (Creutzfeldt–Jakob Disease, Classic)». Centers for Disease Control and Prevention. 26 Φεβρουαρίου 2008. Αρχειοθετήθηκε από το πρωτότυπο στις 6 Μαΐου 2009. Ανακτήθηκε στις 20 Ιουνίου 2009.
«The Nobel Prize in Physiology or Medicine 1997: Stanley B. Prusiner». NobelPrize.org. Αρχειοθετήθηκε από το πρωτότυπο στις 20 Φεβρουαρίου 2011. Ανακτήθηκε στις 21 Φεβρουαρίου 2011.

who.int

«WHO Infection Control Guidelines for Transmissible Spongiform Encephalopathies». World Health Organization: Communicable Disease Surveillance and Control. 26 Μαρτίου 1999. Αρχειοθετήθηκε από το πρωτότυπο στις 18 Μαΐου 2007. Ανακτήθηκε στις 9 Ιουνίου 2007.
«who.int: "Fact sheets no 180: Variant Creutzfeldt–Jakob disease" Feb 2012 ed». Αρχειοθετήθηκε από το πρωτότυπο στις 4 Φεβρουαρίου 2016.

worldcat.org

Manix, Marc; Kalakoti, Piyush; Henry, Miriam; Thakur, Jai; Menger, Richard; Guthikonda, Bharat; Nanda, Anil (2015-11-01). «Creutzfeldt-Jakob disease: updated diagnostic criteria, treatment algorithm, and the utility of brain biopsy» (στα αγγλικά). Neurosurgical Focus 39 (5): E2. doi:10.3171/2015.8.FOCUS15328. ISSN 1092-0684. PMID 26646926.
Atalay, Fatma Oz; Tolunay, Sahsine; Ozgun, Gonca; Bekar, Ahmet; Zarifoglu, Mehmet (2013). «Creutzfeldt-jakob disease: report of four cases and review of the literature». Turkish Journal of Pathology. doi:10.5146/tjpath.2013.01195. ISSN 1018-5615. PMID 24272930. http://www.turkjpath.org/text.php3?doi=10.5146/tjpath.2013.01195.

Νόσος Κρόιτσφελντ-Γιάκομπ (Greek Wikipedia)

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