Works matching Variant Creutzfeldt-Jakob disease

Results: 678

Probable variant Creutzfeldt-Jakob disease in Asia: A case report from Taiwan and review of two prior cases.

Published in:

Psychiatry & Clinical Neurosciences, 2010, v. 64, n. 6, p. 652, doi. 10.1111/j.1440-1819.2010.02151.x

By:

Yang, Chih‐Wen;
Fuh, Jong‐Ling;
Wang, Shuu‐Jiun;
Lirng, Jiing‐Feng;
Yang, Chih‐Chao;
Cheng, Shih‐Jung

Publication type:

Article

Batch recall of French plasma-derived products due to variant Creutzfeldt-Jakob disease risk: the psychological impact on haemophilic patients, changes in their therapeutic demands and behaviour and ethical considerations.

Published in:

Haemophilia, 2015, v. 21, n. 1, p. 27, doi. 10.1111/hae.12515

By:

Aouba, A.;
Harroche, A.;
Frenzel, L.;
Torchet, M. ‐F.;
Rothschild, C.;
François, I.;
Mamzer‐Bruneel, M. ‐F.

Publication type:

Article

Risk reduction strategies for variant Creutzfeldt–Jakob disease transmission by UK plasma products and their impact on patients with inherited bleeding disorders.

Published in:

Haemophilia, 2010, v. 16, n. 2, p. 305, doi. 10.1111/j.1365-2516.2010.02220.x

By:

MILLAR, C. M.;
CONNOR, N.;
DOLAN, G.;
LEE, C. A.;
MAKRIS, M.;
WILDE, J.;
WINTER, M.;
IRONSIDE, J. W.;
GILL, N.;
HILL, F. G. H.

Publication type:

Article

Clinical implications of emerging pathogens in haemophilia: the variant Creutzfeldt–Jakob disease experience.

Published in:

Haemophilia, 2006, v. 12, p. 16, doi. 10.1111/j.1365-2516.2006.01196.x

By:

Dolan, G.

Publication type:

Article

Variant Creutzfeldt–Jakob disease: risk of transmission by blood transfusion and blood therapies.

Published in:

Haemophilia, 2006, v. 12, p. 8, doi. 10.1111/j.1365-2516.2006.01195.x

By:

Ironside, J. W.

Publication type:

Article

The first Japanese patient with variant Creutzfeldt-Jakob disease (vCJD).

Published in:

Neuropathology, 2009, v. 29, n. 6, p. 713, doi. 10.1111/j.1440-1789.2009.01006.x

By:

Shinde, Akiyo;
Kunieda, Takenobu;
Kinoshita, Yoshimi;
Wate, Reika;
Nakano, Satoshi;
Ito, Hidefumi;
Yamada, Masahito;
Kitamoto, Tetsuyuki;
Nakamura, Yosikazu;
Matsumoto, Sadayuki;
Kusaka, Hirofumi

Publication type:

Article

An application of hidden Markov models to the French variant Creutzfeldt-Jakob disease epidemic.

Published in:

Journal of the Royal Statistical Society: Series C (Applied Statistics), 2010, v. 59, n. 5, p. 839, doi. 10.1111/j.1467-9876.2010.00714.x

By:

Chadeau-Hyam, Marc;
Clarke, Paul S.;
Guihenneuc-Jouyaux, Chantal;
Cousens, Simon N.;
Will, Robert G.;
Ghani, Azra C.

Publication type:

Article

Variant Creutzfeldt-Jakob disease strain is identical in individuals of two PRNP codon 129 genotypes.

Published in:

2019

By:

Diack, Abigail B;
Boyle, Aileen;
Plinston, Christopher;
Hunt, Emma;
Bishop, Matthew T;
Will, Robert G;
Manson, Jean C

Publication type:

journal article

A case cluster of variant Creutzfeldt-Jakob disease linked to the Kingdom of Saudi Arabia.

Published in:

Brain: A Journal of Neurology, 2016, v. 139, n. 10, p. 2609, doi. 10.1093/brain/aww206

By:

Coulthart, Michael B.;
Geschwind, Michael D.;
Qureshi, Shireen;
Phielipp, Nicolas;
Demarsh, Alex;
Abrams, Joseph Y.;
Belay, Ermias;
Gambetti, Pierluigi;
Jansen, Gerard H.;
Lang, Anthony E.;
Schonberger, Lawrence B.

Publication type:

Article

Ultrastructural study of florid plaques in variant Creutzfeldt–Jakob disease: a comparison with amyloid plaques in kuru, sporadic Creutzfeldt–Jakob disease and Gerstmann–Sträussler–Scheinker disease.

Published in:

Neuropathology & Applied Neurobiology, 2009, v. 35, n. 1, p. 46, doi. 10.1111/j.1365-2990.2008.00959.x

By:

Sikorska, B.;
Liberski, P. P.;
Sobów, T.;
Budka, H.;
Ironside, J. W.

Publication type:

Article

A quantitative study of the pathological changes in the cerebellum in 15 cases of variant Creutzfeldt–Jakob disease (vCJD).

Published in:

Neuropathology & Applied Neurobiology, 2009, v. 35, n. 1, p. 36, doi. 10.1111/j.1365-2990.2008.00979.x

By:

Armstrong, R. A.;
Ironside, J. W.;
Lantos, P. L.;
Cairns, N. J.

Publication type:

Article

No Adaptation of the Prion Strain in a Heterozygous Case of Variant Creutzfeldt-Jakob Disease.

Published in:

2020

By:

Boyle, Aileen;
Plinston, Chris;
Laing, Fraser;
Mackenzie, Graeme;
Will, Robert G.;
Manson, Jean C.;
Diack, Abigail B.

Publication type:

journal article

Distribution and Quantitative Estimates of Variant Creutzfeldt-Jakob Disease Prions in Tissues of Clinical and Asymptomatic Patients.

Published in:

2017

By:

Douet, Jean Y.;
Lacroux, Caroline;
Aron, Naima;
Head, Mark W.;
Lugan, Séverine;
Tillier, Cécile;
Huor, Alvina;
Cassard, Hervé;
Arnold, Mark;
Beringue, Vincent;
Ironside, James W.;
Andréoletti, Olivier

Publication type:

journal article

Variant Creutzfeldt–Jakob disease: costs borne by families.

Published in:

Health & Social Care in the Community, 2002, v. 10, n. 2, p. 91, doi. 10.1046/j.1365-2524.2002.00346.x

By:

Myles, Susan;
Douglas, Margaret J.;
Ward, Hester J.T.;
Campbell, Harry;
Will, Robert G.

Publication type:

Article

Prion infectivity in the spleen of a PRNP heterozygous individual with subclinical variant Creutzfeldt–Jakob disease.

Published in:

Brain: A Journal of Neurology, 2013, v. 136, n. 4, p. 1139, doi. 10.1093/brain/awt032

By:

Bishop, Matthew T.;
Diack, Abigail B.;
Ritchie, Diane L.;
Ironside, James W.;
Will, Robert G.;
Manson, Jean C.

Publication type:

Article

Survival and Re-Operation Rates after Neurosurgical Procedures in Scotland: Implications for Targeted Surveillance of Sub-Clinical Variant Creutzfeldt-Jakob Disease.

Published in:

Neuroepidemiology, 2009, v. 33, n. 1, p. 1, doi. 10.1159/000209281

By:

Bird, Sheila M.;
Merrall, Elizabeth L.C.;
Ward, Hester J.T.;
Will, Robert G.

Publication type:

Article

Does Poor Dental Health Have a Role in the Emergence of Variant Creutzfeldt Jakob Disease in the United Kingdom?

Published in:

Dental Hypotheses, 2011, v. 2, p. 74, doi. 10.5436/j.dehy.2011.2.00030

By:

Burnie, Robert;
Salmon, Roland L.;
Thomas, Daniel R.;
Monaghan, Nigel

Publication type:

Article

Neuropathological changes in striate and extrastriate visual cortex in variant Creutzfeldt-Jakob disease (vCJD).

Published in:

Clinical Ophthalmology, 2007, v. 1, n. 2, p. 119

By:

Armstrong, Richard A.

Publication type:

Article

Size frequency distribution of prion protein (PrP) aggregates in variant Creutzfeldt-Jakob disease (vCJD).

Published in:

Journal of Neural Transmission, 2005, v. 112, n. 11, p. 1565, doi. 10.1007/s00702-005-0296-2

By:

Armstrong, R. A.;
Cairns, N. J.;
Ironside, J. W.;
Lantos, P. L.

Publication type:

Article

Spatial correlations between the vacuolation, prion protein deposition and surviving neurons in variant Creutzfeldt-Jakob Disease (vCJD).

Published in:

Journal of Neural Transmission, 2003, v. 110, n. 11, p. 1303, doi. 10.1007/s00702-003-0039-1

By:

Armstrong, R. A.;
Lantos, P. L.;
Ironside, J. W.;
Cairns, N. J.

Publication type:

Article

Dealing with the uncertain risk of variant Creutzfeldt- Jakob disease transmission by coagulation replacement products.

Published in:

British Journal of Haematology, 2012, v. 158, n. 4, p. 442, doi. 10.1111/j.1365-2141.2012.09201.x

By:

Millar, Carolyn M.;
Makris, Mike

Publication type:

Article

Smallde novoduplication in the repeat region of the TATA-box-binding protein gene manifest with a phenotype similar to variant Creutzfeldt-Jakob disease.

Published in:

Clinical Genetics, 2004, v. 66, n. 6, p. 496, doi. 10.1111/j.1399-0004.2004.00356.x

By:

Shatunov, A.;
Fridman, E. A.;
Pagan, F. I.;
Leib, J.;
Singleton, A.;
Hallett, M.;
Goldfarb, L. G.

Publication type:

Article

Variant Creutzfeldt-Jakob disease: an unfolding epidemic of misfolded proteins.

Published in:

2002

By:

Horby, P

Publication type:

journal article

The spatial patterns of prion protein deposits in cases of variant Creutzfeldt-Jakob disease.

Published in:

Acta Neuropathologica, 2002, v. 104, n. 6, p. 665, doi. 10.1007/s00401-002-0598-5

By:

Armstrong, R. A.;
Cairns, N. J.;
Ironside, J. W.;
Lantos, P. L.

Publication type:

Article

Electron microsocopy of brain amyloid plaques from a patient with new variant Creutzfeldt-Jakob disease.

Published in:

Acta Neuropathologica, 2000, v. 99, n. 6, p. 637, doi. 10.1007/s004010051174

By:

Fournier, Jean-Guy;
Kopp, Nicolas;
Streichenberger, Nathalie;
Escaig-Haye, Françoise;
Langeveld, Jan;
Brown, Paul

Publication type:

Article

Size frequency distributions of the florid prion protein aggregates in variant Creutzfeldt-Jakob disease follow a power-law function.

Published in:

2006

By:

Armstrong, R.;
Cairns, N.;
Ironside, J.;
Armstrong, R A;
Cairns, N J;
Ironside, J W

Publication type:

journal article

Comparison of the neuropathological characteristics of bovine spongiform encephalopathy (BSE) and variant Creutzfeldt–Jakob disease (vCJD) in mice.

Published in:

Neuropathology & Applied Neurobiology, 2003, v. 29, n. 3, p. 262, doi. 10.1046/j.1365-2990.2003.00462.x

By:

Brown, D. A.;
Bruce, M. E.;
Fraser, J. R.

Publication type:

Article

Quantification of vacuolation (‘spongiform change’), surviving neurones and prion protein deposition in eleven cases of variant Creutzfeldt–Jakob disease.

Published in:

Neuropathology & Applied Neurobiology, 2002, v. 28, n. 2, p. 129, doi. 10.1046/j.1365-2990.2002.00386.x

By:

Armstrong, R. A;
Cairns, N. J;
Ironside, J. W;
Lantos, P. L

Publication type:

Article

Preclinical Detection of Prions in Blood of Nonhuman Primates Infected with Variant Creutzfeldt-Jakob Disease.

Published in:

2020

By:

Concha-Marambio, Luis;
Chacon, Marcelo A.;
Soto, Claudio

Publication type:

journal article

Diagnosis of Methionine/Valine Variant Creutzfeldt-Jakob Disease by Protein Misfolding Cyclic Amplification.

Published in:

2018

By:

Bougard, Daisy;
Bélondrade, Maxime;
Mayran, Charly;
Bruyère-Ostells, Lilian;
Lehmann, Sylvain;
Fournier-Wirth, Chantal;
Knight, Richard S.;
Will, Robert G.;
Green, Alison J. E.

Publication type:

journal article

Protective Effect of Val<sub>129</sub>-PrP against Bovine Spongiform Encephalopathy but not Variant Creutzfeldt-Jakob Disease.

Published in:

2017

By:

Fernández-Borges, Natalia;
Espinosa, Juan Carlos;
Marín-Moreno, Alba;
Aguilar-Calvo, Patricia;
Asante, Emmanuel A.;
Tetsuyuki Kitamoto;
Shirou Mohri;
Andréoletti, Olivier;
Torres, Juan María;
Kitamoto, Tetsuyuki;
Mohri, Shirou

Publication type:

journal article

Has the frequency of ABO RhD blood groups in Australian blood donors changed as a result of the removal of the variant Creutzfeldt–Jakob disease‐based deferral?

Published in:

Vox Sanguinis, 2024, v. 119, n. 6, p. 619, doi. 10.1111/vox.13614

By:

Hirani, Rena;
Hoad, Veronica C.;
Gosbell, Iain B.;
Irving, David O.

Publication type:

Article

Risk of variant Creutzfeldt–Jakob disease transmission by blood transfusion in Australia.

Published in:

Vox Sanguinis, 2022, v. 117, n. 8, p. 1016, doi. 10.1111/vox.13290

By:

McManus, Hamish;
Seed, Clive R.;
Hoad, Veronica C.;
Kiely, Philip;
Kaldor, John M.;
Styles, Claire E.;
Yang, Hong;
Law, Matthew;
Gosbell, Iain B.

Publication type:

Article

Risks of transmission of variant Creutzfeldt-Jakob disease by blood transfusion.

Published in:

Folia Neuropathologica, 2005, v. 43, n. 4, p. 271

By:

Peden, Alexander H.;
Ritchie, Diane L.;
Ironside, James W.

Publication type:

Article

Diagnostic accuracy of diffusion-weighted imaging in variant Creutzfeldt–Jakob disease.

Published in:

Neuroradiology, 2023, v. 65, n. 12, p. 1715, doi. 10.1007/s00234-023-03230-w

By:

Mackenzie, G.;
Summers, D.;
Mackenzie, J.;
Knight, R.

Publication type:

Article

Sensory features of variant Creutzfeldt-Jakob disease.

Published in:

Journal of Neurology, 2002, v. 249, n. 6, p. 706, doi. 10.1007/s00415-002-0696-2

By:

Macleod, M.-A.;
Stewart, G. E.;
Zeidler, M.;
Will, R.;
Knight, R.

Publication type:

Article

Variant Creutzfeldt–Jakob disease: first two indigenous cases in Republic of Ireland. Case report and perspective.

Published in:

European Journal of Neurology, 2007, v. 14, n. 4, p. 467, doi. 10.1111/j.1468-1331.2007.01643.x

By:

McHugh, J. C.;
Bradley, D.;
Hutchinson, M.;
Brett, F.;
Heffernan, J.;
Howley, R.;
Farrell, M.;
Tubridy, N.

Publication type:

Article

Heidenhain variant of Creutzfeldt–Jakob disease resembles dementia with Lewy bodies.

Published in:

Psychogeriatrics, 2021, v. 21, n. 1, p. 121, doi. 10.1111/psyg.12640

By:

Tokumitsu, Keita;
Oyama, Shigeto;
Takeuchi, Junko;
Yachimori, Koji;
Sugawara, Norio;
Yasui‐Furukori, Norio;
Shimoda, Kazutaka

Publication type:

Article

Universal leucodepletion to reduce the risk of transmission of new-variant creutzfeldt–jakob disease.

Published in:

British Journal of Haematology, 2000, v. 110, n. 1, p. 234, doi. 10.1046/j.1365-2141.2000.02072.x

By:

Sivakumaran, M.

Publication type:

Article

Heidenhain variant of Creutzfeldt-Jakob disease in a patient who had bovine bioprosthetic valve implantation.

Published in:

2016

By:

Hashoul, Jehard;
Saliba, Waleed;
Bloch, Irina;
Jabaly-Habib, Haneen

Publication type:

journal article

Unusual Dopaminergic Depletion in Variant Creutzfeldt-Jakob Disease with Early and Rapid Cognitive Decline.

Published in:

European Neurology, 2011, v. 65, n. 6, p. 368, doi. 10.1159/000328670

By:

Magnin, Eloi;
Chopard, Gilles;
Galmiche, Jean;
Brandel, Jean-Philippe;
Rumbach, Lucien

Publication type:

Article

Prion protein heterogeneity in sporadic but not variant Creutzfeldt-Jakob disease: U.K. cases 1991-2002.

Published in:

2004

By:

Head MW;
Bunn TJR;
Bishop MT;
McLoughlin V;
Lowrie S;
McKimmie CS;
Williams MC;
McCardle L;
MacKenzie J;
Knight R;
Will RG;
Ironside JW

Publication type:

Journal Article

Prion protein heterogeneity in sporadic but not variant CreutzfeldtJakob disease: U.K. cases 19912002.

Published in:

Annals of Neurology, 2004, v. 55, n. 6, p. 851

By:

Mark W. Head;
Tristan J. R. Bunn;
Matthew T. Bishop;
Victoria McLoughlin;
Suzanne Lowrie;
Clive S. McKimmie;
Michelle C. Williams;
Linda McCardle;
Jan MacKenzie;
Richard Knight;
Robert G. Will;
James W. Ironside

Publication type:

Article

Clearance of variant Creutzfeldt-Jakob disease prions in vivo by the Hsp70 disaggregase system.

Published in:

2022

By:

Thackray, Alana M;
Lam, Brian;
McNulty, Erin E;
Nalls, Amy V;
Mathiason, Candace K;
Magadi, Srivathsa Subramanya;
Jackson, Walker S;
Andréoletti, Olivier;
Marrero-Winkens, Cristóbal;
Schätzl, Hermann;
Bujdoso, Raymond

Publication type:

journal article

RNA integrity in post mortem human variant Creutzfeldt-Jakob disease (vCJD) and control brain tissue.

Published in:

Neuropathology & Applied Neurobiology, 2011, v. 37, n. 6, p. 633, doi. 10.1111/j.1365-2990.2011.01162.x

By:

Sherwood, K. R.;
Head, M. W.;
Walker, R.;
Smith, C.;
Ironside, J. W.;
Fazakerley, J. K.

Publication type:

Article

Reduplicative paramnesia as an atypical form of presentation of a Heidenhain variant of Creutzfeldt-Jakob disease: A case report.

Published in:

Journal of the International Neuropsychological Society, 2023, v. 29, n. 6, p. 615, doi. 10.1017/S1355617722000583

By:

Martinez-Horta, Saul;
Marzal-Espí, Clara Naima;
Cusó-García, Silvia;
Aracil-Bolaños, Ignacio;
Kulisevsky, Jaime

Publication type:

Article

Correlation of Polydispersed Prion Protein and Characteristic Pathology in the Thalamus in Variant Creutzfeldt-Jakob Disease: Implication of Small Oligomeric Species.

Published in:

Brain Pathology, 2011, v. 21, n. 3, p. 298, doi. 10.1111/j.1750-3639.2010.00446.x

By:

Choi, Young Pyo;
Gröner, Albrecht;
Ironside, James W.;
Head, Mark W.

Publication type:

Article

Splice site SNPs of phospholipase PLCXD3 are significantly associated with variant and sporadic Creutzfeldt-Jakob disease.

Published in:

BMC Medical Genetics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2350-14-91

By:

Bishop, Matthew T.;
Sanchez-Juan, Pascual;
Knight, Richard S. G.

Publication type:

Article

Prion infectivity in the spleen of a PRNP heterozygous individual with subclinical variant Creutzfeldt-Jakob disease.

Published in:

2013

By:

Bishop, Matthew T;
Diack, Abigail B;
Ritchie, Diane L;
Ironside, James W;
Will, Robert G;
Manson, Jean C

Publication type:

journal article

The Heidenhain variant of Creutzfeldt–Jakob disease.

Published in:

2018

By:

Hunt, Alex;
Ibrahim, Kasim;
Rahmani, Muhammad JH

Publication type:

Case Study