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ALLMedicine™ Creutzfeldt-jakob Disease Center

Research & Reviews  1,999 results

Biomarkers and diagnostic guidelines for sporadic Creutzfeldt-Jakob disease.
https://doi.org/10.1016/S1474-4422(20)30477-4
The Lancet. Neurology; Hermann P, Appleby B et. al.

Feb 20th, 2021 - Sporadic Creutzfeldt-Jakob disease is a fatal neurodegenerative disease caused by misfolded prion proteins (PrPSc). Effective therapeutics are currently not available and accurate diagnosis can be challenging. Clinical diagnostic criteria use a co...

Preclinical transmission of prions by blood transfusion is influenced by donor genotype...
https://doi.org/10.1371/journal.ppat.1009276
PLoS Pathogens; Salamat MKF, Blanco ARA et. al.

Feb 18th, 2021 - Variant Creutzfeldt-Jakob disease (vCJD) is a human prion disease resulting from zoonotic transmission of bovine spongiform encephalopathy (BSE). Documented cases of vCJD transmission by blood transfusion necessitate on-going risk reduction measur...

Lower motor neuron signs as part of the clinical spectrum of Creutzfeldt-Jakob disease:...
https://doi.org/10.1016/j.clineuro.2021.106535
Clinical Neurology and Neurosurgery; Serrazina F, Fernandes M et. al.

Feb 4th, 2021 - Lower motor neuron signs as part of the clinical spectrum of Creutzfeldt-Jakob disease: A histopathological correlation.|2021|Serrazina F,Fernandes M,Guimarães S,Caetano A,|

Wide distribution of prion infectivity in the peripheral tissues of vCJD and sCJD patie...
https://doi.org/10.1007/s00401-021-02270-x 10.1006/nbdi.2002.0558 10.1371/journal.ppat.1002782 10.1051/vetres:2008046 10.1128/JVI.66.4.2096-2101.1992 10.1128/JVI.68.12.7859-7868.1994 10.1073/pnas.1004688107 10.1126/scitranslmed.aag1257 10.3201/eid1806.120116 10.1002/ana.410350504 10.1128/mBio.00393-20 10.1038/ncomms6821 10.1007/s00705-002-0958-4 10.1101/cshperspect.a006833 10.3201/eid2306.161734 10.1128/JVI.02783-15 10.3201/eid2001.130353 10.1074/jbc.M407006200 10.1007/BF03401958 10.1016/0021-9975(73)90024-8 10.1016/0021-9975(68)90006-6 10.1007/s00401-020-02153-7 10.1136/bmj.f5675 10.1056/NEJMoa030351 10.1016/j.jhin.2014.06.002 10.1038/sj.bdj.4810536 10.1016/S0002-9440(10)63105-7 10.1016/S0140-6736(98)12075-5 10.1016/S0140-6736(97)24002-X 10.1002/path.4954 10.1128/JVI.01383-16 10.1007/s00401-010-0713-y 10.1371/journal.ppat.1004202 10.1111/j.1537-2995.2008.02044.x 10.1016/S0140-6736(04)15486-X 10.1001/jamaneurol.2016.3733 10.1308/003588408X261726 10.1002/sim.4780140812 10.1016/0092-8674(83)90207-6 10.1007/s00705-007-0956-7 10.1126/scitranslmed.aam7785 10.1371/journal.ppat.1001319 10.1002/ana.410390613 10.1111/j.1365-2516.2009.02181.x 10.1016/S0140-6736(04)16811-6 10.1136/jnnp-2018-318756 10.1126/science.6801762 10.1159/000503234 10.1128/JVI.75.21.10106-10112.2001 10.1016/j.ebiom.2016.08.033 10.1016/S1631-0691(02)01386-0 10.1016/j.jocn.2013.01.007 10.1016/S0268-960X(98)90007-8 10.1016/B978-0-444-63945-5.00009-X
Acta Neuropathologica; Douet JY, Huor A et. al.

Feb 3rd, 2021 - Sporadic Creutzfeldt-Jakob disease (sCJD) is the commonest human prion disease, occurring most likely as the consequence of spontaneous formation of abnormal prion protein in the central nervous system (CNS). Variant Creutzfeldt-Jakob disease (vCJ...

Palliative care in Creutzfeldt-Jakob disease: looking back, thinking ahead.
https://doi.org/10.1136/bmjspcare-2020-002799
BMJ Supportive & Palliative Care; De Vries K, Cousins E et. al.

Jan 23rd, 2021 - Creutzfeldt-Jakob disease (CJD) is a rare and fatal neurodegenerative disease for which there is no cure. However, it is difficult to diagnose and is unique in that it is both a genetic and transmissible disease. The disease is characterised by sy...

see more →

Clinicaltrials.gov  2,107 results

Biomarkers and diagnostic guidelines for sporadic Creutzfeldt-Jakob disease.
https://doi.org/10.1016/S1474-4422(20)30477-4
The Lancet. Neurology; Hermann P, Appleby B et. al.

Feb 20th, 2021 - Sporadic Creutzfeldt-Jakob disease is a fatal neurodegenerative disease caused by misfolded prion proteins (PrPSc). Effective therapeutics are currently not available and accurate diagnosis can be challenging. Clinical diagnostic criteria use a co...

Preclinical transmission of prions by blood transfusion is influenced by donor genotype...
https://doi.org/10.1371/journal.ppat.1009276
PLoS Pathogens; Salamat MKF, Blanco ARA et. al.

Feb 18th, 2021 - Variant Creutzfeldt-Jakob disease (vCJD) is a human prion disease resulting from zoonotic transmission of bovine spongiform encephalopathy (BSE). Documented cases of vCJD transmission by blood transfusion necessitate on-going risk reduction measur...

Lower motor neuron signs as part of the clinical spectrum of Creutzfeldt-Jakob disease:...
https://doi.org/10.1016/j.clineuro.2021.106535
Clinical Neurology and Neurosurgery; Serrazina F, Fernandes M et. al.

Feb 4th, 2021 - Lower motor neuron signs as part of the clinical spectrum of Creutzfeldt-Jakob disease: A histopathological correlation.|2021|Serrazina F,Fernandes M,Guimarães S,Caetano A,|

Wide distribution of prion infectivity in the peripheral tissues of vCJD and sCJD patie...
https://doi.org/10.1007/s00401-021-02270-x 10.1006/nbdi.2002.0558 10.1371/journal.ppat.1002782 10.1051/vetres:2008046 10.1128/JVI.66.4.2096-2101.1992 10.1128/JVI.68.12.7859-7868.1994 10.1073/pnas.1004688107 10.1126/scitranslmed.aag1257 10.3201/eid1806.120116 10.1002/ana.410350504 10.1128/mBio.00393-20 10.1038/ncomms6821 10.1007/s00705-002-0958-4 10.1101/cshperspect.a006833 10.3201/eid2306.161734 10.1128/JVI.02783-15 10.3201/eid2001.130353 10.1074/jbc.M407006200 10.1007/BF03401958 10.1016/0021-9975(73)90024-8 10.1016/0021-9975(68)90006-6 10.1007/s00401-020-02153-7 10.1136/bmj.f5675 10.1056/NEJMoa030351 10.1016/j.jhin.2014.06.002 10.1038/sj.bdj.4810536 10.1016/S0002-9440(10)63105-7 10.1016/S0140-6736(98)12075-5 10.1016/S0140-6736(97)24002-X 10.1002/path.4954 10.1128/JVI.01383-16 10.1007/s00401-010-0713-y 10.1371/journal.ppat.1004202 10.1111/j.1537-2995.2008.02044.x 10.1016/S0140-6736(04)15486-X 10.1001/jamaneurol.2016.3733 10.1308/003588408X261726 10.1002/sim.4780140812 10.1016/0092-8674(83)90207-6 10.1007/s00705-007-0956-7 10.1126/scitranslmed.aam7785 10.1371/journal.ppat.1001319 10.1002/ana.410390613 10.1111/j.1365-2516.2009.02181.x 10.1016/S0140-6736(04)16811-6 10.1136/jnnp-2018-318756 10.1126/science.6801762 10.1159/000503234 10.1128/JVI.75.21.10106-10112.2001 10.1016/j.ebiom.2016.08.033 10.1016/S1631-0691(02)01386-0 10.1016/j.jocn.2013.01.007 10.1016/S0268-960X(98)90007-8 10.1016/B978-0-444-63945-5.00009-X
Acta Neuropathologica; Douet JY, Huor A et. al.

Feb 3rd, 2021 - Sporadic Creutzfeldt-Jakob disease (sCJD) is the commonest human prion disease, occurring most likely as the consequence of spontaneous formation of abnormal prion protein in the central nervous system (CNS). Variant Creutzfeldt-Jakob disease (vCJ...

Palliative care in Creutzfeldt-Jakob disease: looking back, thinking ahead.
https://doi.org/10.1136/bmjspcare-2020-002799
BMJ Supportive & Palliative Care; De Vries K, Cousins E et. al.

Jan 23rd, 2021 - Creutzfeldt-Jakob disease (CJD) is a rare and fatal neurodegenerative disease for which there is no cure. However, it is difficult to diagnose and is unique in that it is both a genetic and transmissible disease. The disease is characterised by sy...

see more →

News  107 results

Fast Five Quiz: Alzheimer Disease Differential Diagnosis and Workup
https://reference.medscape.com/viewarticle/912046_2

May 22nd, 2019 - Answer 1/5 Memory-sparing can be observed with which of the following in the early stages of dementia? Your peers chose: Alzheimer disease and frontotemporal dementia (FTD) 0% Chronic traumatic encephalopathy (CTE) and FTD 0% Dementia with Lewy bo...

CSF and plasma biomarkers predict survival in sporadic Creutzfeldt-Jakob disease
https://www.mdedge.com/neurology/article/200209/rare-diseases/csf-and-plasma-biomarkers-predict-survival-sporadic/page/0/1?channel=27970

May 6th, 2019 - Plasma total tau was associated with survival In all, 188 patients were included in the analysis. The population’s mean age was 63.

Fast Five Quiz: Organ Donation and Transplant
https://reference.medscape.com/viewarticle/905709_2

Dec 5th, 2018 - Answer 1/5 Although regional transplant centers have varying sets of absolute and relative criteria for excluding potential donors, which of the following is currently considered an absolute contraindication in a deceased donor, according to the N...

Eye Testing May Aid Early Diagnosis of Creutzfeldt-Jakob Disease
https://www.medscape.com/viewarticle/905720

Nov 27th, 2018 - Eye examinations may aid clinicians in the diagnosis of sporadic Creutzfeldt-Jacob disease (sCJD), results of a small postmortem study show. In an evaluation of the eyes and brains of 11 sCJD patients, investigators found prion seeding in all eyes...

Eye Testing May Aid Early Diagnosis of Creutzfeldt-Jakob Disease
https://www.staging.medscape.com/viewarticle/905720

Nov 27th, 2018 - Eye examinations may aid clinicians in the diagnosis of sporadic Creutzfeldt-Jacob disease (sCJD), results of a small postmortem study show. In an evaluation of the eyes and brains of 11 sCJD patients, investigators found prion seeding in all eyes...

see more →

Patient Education  13 results see all →