Works matching Creutzfeldt-Jakob disease

Results: 3648

Overview and evaluation of 15 years of Creutzfeldt-Jakob disease surveillance in Belgium, 1998-2012.

Published in:

2015

By:

Litzroth, Amber;
Cras, Patrick;
De Vil, Bart;
Quoilin, Sophie

Publication type:

journal 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

Visual art therapy in sporadic Creutzfeldt-Jakob disease: a case study.

Published in:

2016

By:

Shrestha, Rajeet;
Trauger-Querry, Barbara;
Loughrin, Athena;
Appleby, Brian S.

Publication type:

journal article

Bilateral Vestibular Failure as an Early Sign in Creutzfeldt-Jakob Disease.

Published in:

Annals of the New York Academy of Sciences, 2009, v. 1164, p. 390, doi. 10.1111/j.1749-6632.2008.03741.x

By:

Jahn, Klaus;
Arbusow, Viktor;
Zingler, Vera C.;
Strupp, Michael;
Kretzschmar, Hans A.;
Brandt, Thomas

Publication type:

Article

Komorbidní Creutzfeldtova-Jakobova choroba jako diagnostická svízel: kazuistické sdělení kombinace čtyř různých neurodegenerací a pokročilých vaskulárních změn.

Published in:

Neurologie Pro Praxi, 2024, v. 25, n. 1, p. 41, doi. 10.36290/neu.2024.001

By:

Jankovská, Nikol;
Waishaupt, Jan;
Holada, Karel;
Matěj, Radoslav

Publication type:

Article

Identification of Novel Proteins for Creutzfeldt-Jakob Disease by Integrating Genome-wide Association Data and Human Brain Proteomes.

Published in:

Chinese Journal of Biochemistry & Molecular Biology, 2025, v. 41, n. 7, p. 1040, doi. 10.13865/j.enki.cjbmb.2025.06.1087

By:

ZHONG Wan-Ting;
YUAN Yi-Tong;
ZHANG Min;
DU Ruo-Chen;
ZHANG Ling-Yu;
WANG Chun-Fang

Publication type:

Article

Non-convulsive status epilepticus versus periodic EEG pattern in sporadic Creutzfeldt-Jakob disease: two sides of the same coin?

Published in:

2024

By:

Fanella, Martina;
Valente, Giada;
Borrello, Laura;
Marinelli, Fabiana;
Bracaglia, Martina;
Di Marco, Ottavio;
Costanzo, Filippo;
Apponi, Fabrizio;
De Simone, Roberto

Publication type:

Case Study

A case of MV2K subtype of sporadic Creutzfeldt–Jakob disease with florid‐like plaques: Similarities and differences to variant Creutzfeldt–Jakob disease.

Published in:

Neuropathology, 2020, v. 40, n. 4, p. 389, doi. 10.1111/neup.12652

By:

Bošnjak, Matic;
Zupan, Andrej;
Fiorini, Michele;
Popović, Katarina Š.;
Popović, Mara

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

Cerebral amyloid angiopathy with co-localization of prion protein and beta-amyloid in an 85-year-old patient with sporadic Creutzfeldt–Jakob disease.

Published in:

2008

By:

Paquet, Claire;
Privat, Nicolas;
Kaci, Rachid;
Polivka, Marc;
Dupont, Olivier;
Haïk, Stéphane;
Laplanche, Jean Louis;
Hauw, Jean Jacques;
Gray, Françoise

Publication type:

Report

Creutzfeldt–Jakob disease and ENT.

Published in:

Journal of Laryngology & Otology, 2013, v. 127, n. 11, p. 1050, doi. 10.1017/S002221511300234X

By:

Sethi, N;
Kane, J;
Condon, L

Publication type:

Article

A case of dementia with Lewy bodies that temporarily showed symptoms similar to Creutzfeldt-Jakob disease.

Published in:

Psychogeriatrics, 2010, v. 10, n. 4, p. 201, doi. 10.1111/j.1479-8301.2010.00336.x

By:

UKAI, Katsuyuki;
MATSUO, Koji;
NAKAMURA, Ryoichi;
SOBUE, Gen;
KOSAKA, Kenji;
SHIBAYAMA, Hiroto;
IRITANI, Shuji;
ISHIHARA, Ryoko;
OZAKI, Norio

Publication type:

Article

Right parietal lobe syndrome as a clinical variant of Creutzfeldt-Jakob disease.

Published in:

Psychogeriatrics, 2006, v. 6, n. 2, p. 74, doi. 10.1111/j.1479-8301.2006.00154.x

By:

Komuro, Ryutaro;
Kobayashi, Katsuji;
Shimazaki, Masao;
Sugimori, Kaoru;
Koshino, Yoshifumi;
Satou, Katsuaki;
Oda, Yoshio

Publication type:

Article

Assessing the newly proposed MRI criteria for diagnosing sporadic Creutzfeldt-Jakob disease.

Published in:

Neuroradiology, 2024, v. 66, n. 11, p. 1907, doi. 10.1007/s00234-024-03440-w

By:

Barber, Daniel;
Trost, Nicholas;
Stehmann, Christiane;
Lewis, Victoria;
Doecke, James;
Jhamb, Ash;
Winata, Shin-han Leon;
Collins, Steven

Publication type:

Article

Incidence of Creutzfeldt-Jakob disease in Taiwan: a prospective 10-year surveillance.

Published in:

European Journal of Epidemiology, 2010, v. 25, n. 5, p. 341, doi. 10.1007/s10654-010-9446-4

By:

Chien-Jung Lu;
Yu Sun;
Shun-Sheng Chen

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

Coexistence of Creutzfeldt-Jakob disease, Lewy body disease, and Alzheimer's disease pathology: An autopsy case showing typical clinical features of Creutzfeldt-Jakob disease.

Published in:

Neuropathology, 2009, v. 29, n. 4, p. 454, doi. 10.1111/j.1440-1789.2008.00964.x

By:

Haraguchi, Takashi;
Terada, Seishi;
Ishizu, Hideki;
Sakai, Kenichi;
Tanabe, Yasuyuki;
Nagai, Taiji;
Takata, Hiroshi;
Nobukuni, Keigo;
Ihara, Yuetsu;
Kitamoto, Tetsuyuki;
Kuroda, Shigetoshi

Publication type:

Article

Clinicopathologic characteristics of five autopsied cases of dura mater-associated Creutzfeldt-Jakob disease.

Published in:

Neuropathology, 2008, v. 28, n. 1, p. 51, doi. 10.1111/j.1440-1789.2007.00847.x

By:

Iwasaki, Yasushi;
Mimuro, Maya;
Yoshida, Mari;
Hashizume, Yoshio;
Kitamoto, Tetsuyuki;
Sobue, Gen

Publication type:

Article

A sporadic case of Creutzfeldt–Jakob disease with beta-amyloid deposits and alpha-synuclein inclusions.

Published in:

Neuropathology, 2007, v. 27, n. 3, p. 273, doi. 10.1111/j.1440-1789.2007.00755.x

By:

Vital, Anne;
Canron, Marie-Hélène;
Gil, Roger;
Hauw, Jean-Jacques;
Vital, Claude

Publication type:

Article

Severe cortical involvement in MV2 Creutzfeldt–Jakob disease: An autopsy case report.

Published in:

Neuropathology, 2006, v. 26, n. 5, p. 433, doi. 10.1111/j.1440-1789.2006.00705.x

By:

Ishihara, Kenji;
Sugie, Masayuki;
Shiota, Jun-ichi;
Kawamura, Mitsuru;
Kitamoto, Tetsuyuki;
Nakano, Imaharu

Publication type:

Article

Creutzfeldt–Jakob disease risk and PRNP codon 129 polymorphism: necessity to revalue current data.

Published in:

European Journal of Neurology, 2005, v. 12, n. 12, p. 998, doi. 10.1111/j.1468-1331.2005.01110.x

By:

Mitrová, E.;
Mayer, V.;
Jovankoviçová, V.;
Slivarichová, D.;
Wsólová, L.

Publication type:

Article

Sporadic Creutzfeldt-Jakob disease in Northern Tasmania.

Published in:

Journal of the Royal College of Physicians of Edinburgh, 2023, v. 53, n. 1, p. 35, doi. 10.1177/14782715221150580

By:

Rajalingam, Priyanka;
de Souza, Aaron;
Lee-Archer, Matthew;
Dhakal, Mahesh

Publication type:

Article

MRI Detection of the Cerebellar Syndrome in Creutzfeldt–Jakob Disease.

Published in:

Cerebellum, 2009, v. 8, n. 3, p. 373, doi. 10.1007/s12311-009-0106-8

By:

Cohen, Oren S.;
Hoffmann, Chen;
Lee, Hedok;
Chapman, Joab;
Fulbright, Robert K.;
Prohovnik, Isak

Publication type:

Article

The first reported case of Creutzfeldt‐Jakob disease from Nepal.

Published in:

Clinical Case Reports, 2020, v. 8, n. 1, p. 198, doi. 10.1002/ccr3.2609

By:

Kharel, Himal;
Adhikari, Pabitra;
Pokhrel, Nishan B.;
Kharel, Zeni;
Nepal, Gaurav

Publication type:

Article

Intestinal pseudo-obstruction in Creutzfeldt-Jakob disease.

Published in:

2021

By:

Videira, Gonçalo;
Ferro, Daniela;
Guimarães, Susana;
Pinto, Madalena;
Santos, Ernestina

Publication type:

Letter

Creutzfeldt-Jakob disease: a single institution case series.

Published in:

International Journal of Palliative Nursing, 2024, v. 30, n. 12, p. 630, doi. 10.12968/ijpn.2024.30.12.630

By:

Waran, Eswaran;
Bach, Danielle;
Amos, Jo-Anne

Publication type:

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

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

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

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

Ophthalmic manifestation of Creutzfeldt-Jakob disease in the Heidenhain variant - a case report.

Published in:

2020

By:

Linke, Anna;
Cisiecki, Sławomir;
Bonińska, Karolina;
Bednarski, Maciej

Publication type:

Case Study

Sporadic Creutzfeldt-Jakob Disease with Psychiatric Symptoms: A Case Report.

Published in:

Turk Psikiyatri Dergisi, 2015, v. 26, n. 3, p. 1

By:

ÖZKAN, Adile;
AYDIN CANTÜRK, İlknur;
CANDAN, Fatma;
IŞIK, Nihal;
ÖZISIK KAHRAMAN, Handan Isin

Publication type:

Article

Enhanced Creutzfeldt‐Jakob disease surveillance in the older population: Assessment of a protocol for screening brain tissue donations for prion disease.

Published in:

Brain Pathology, 2024, v. 34, n. 2, p. 1, doi. 10.1111/bpa.13214

By:

Peden, Alexander H.;
Libori, Adriana;
Ritchie, Diane L.;
Yull, Helen;
Smith, Colin;
Kanguru, Lovney;
Molesworth, Anna;
Knight, Richard;
Barria, Marcelo A.

Publication type:

Article

Tau pathology in Creutzfeldt-Jakob disease revisited.

Published in:

Brain Pathology, 2017, v. 27, n. 3, p. 332, doi. 10.1111/bpa.12411

By:

Kovacs, Gabor G.;
Rahimi, Jasmin;
Ströbel, Thomas;
Lutz, Mirjam I.;
Regelsberger, Günther;
Streichenberger, Nathalie;
Perret‐Liaudet, Armand;
Höftberger, Romana;
Liberski, Pawel P.;
Budka, Herbert;
Sikorska, Beata

Publication type:

Article

Sporadic Creutzfeldt-Jakob Disease MM1+2C and MM1 are Identical in Transmission Properties.

Published in:

Brain Pathology, 2016, v. 26, n. 1, p. 95, doi. 10.1111/bpa.12264

By:

Kobayashi, Atsushi;
Matsuura, Yuichi;
Iwaki, Toru;
Iwasaki, Yasushi;
Yoshida, Mari;
Takahashi, Hitoshi;
Murayama, Shigeo;
Takao, Masaki;
Kato, Shinsuke;
Yamada, Masahito;
Mohri, Shirou;
Kitamoto, Tetsuyuki

Publication type:

Article

Symptomatic aggravation after corticosteroid pulse therapy in definite sporadic Creutzfeldt-Jakob disease with the feature of Hashimoto's encephalopathy.

Published in:

BMC Neurology, 2014, v. 14, n. 1, p. 1, doi. 10.1186/s12883-014-0179-y

By:

Jae-Won Jang;
So Young Park;
Young Ho Park;
Jung E Kim;
SangYun Kim

Publication type:

Article

Creutzfeldt-Jakob Disease After the Coronavirus Disease-2019 Vaccination.

Published in:

2022

By:

Kuvandık, Anıl;
Özcan, Ecenur;
Karaduman, Simay;
Sungurtekin, Hülya

Publication type:

Case Study

The Role of Neuroimaging in Evaluating Patients Affected by Creutzfeldt-Jakob Disease: A Systematic Review of the Literature.

Published in:

Journal of Neuroimaging, 2015, v. 25, n. 1, p. 2, doi. 10.1111/jon.12098

By:

Caobelli, Federico;
Cobelli, Milena;
Pizzocaro, Claudio;
Pavia, Marco;
Magnaldi, Silvia;
Guerra, Ugo Paolo

Publication type:

Article

Variability in Diagnosing Creutzfeldt-Jakob Disease Using Standard and Proposed Diagnostic Criteria.

Published in:

Journal of Neuroimaging, 2013, v. 23, n. 1, p. 58, doi. 10.1111/j.1552-6569.2012.00763.x

By:

Newey, C. R.;
Sarwal, A.;
Wisco, D.;
Alam, S.;
Lederman, R. J.

Publication type:

Article

A Case of Creutzfeldt–Jakob disease with psychiatric presentation.

Published in:

Journal of Geriatric Mental Health, 2024, v. 11, n. 1, p. 60, doi. 10.4103/jgmh.jgmh_15_24

By:

Dutta, Anirban;
Das, Sameeksha;
Harbishettar, Vijaykumar

Publication type:

Article

Sporadic Creutzfeldt-Jakob Disease: Diagnosing Typical and Atypical Presentations under Limited Circumstances.

Published in:

Dementia & Geriatric Cognitive Disorders, 2021, v. 50, n. 1, p. 36, doi. 10.1159/000514470

By:

Khan, Shazma;
Khan, Sara

Publication type:

Article

D178N, 129Val and N171S, 129Val Genotype in a Family with Creutzfeldt-Jakob Disease.

Published in:

Dementia & Geriatric Cognitive Disorders, 2010, v. 30, n. 5, p. 424, doi. 10.1159/000321472

By:

Appleby, Brian S.;
Appleby, Kristin K.;
Hall, Ryan C. W.;
Wallin, Mitchell T.

Publication type:

Article

Prospective Study Demonstrates Utility of EP-QuIC in Creutzfeldt–Jakob Disease Diagnoses.

Published in:

Canadian Journal of Neurological Sciences, 2021, v. 48, n. 1, p. 127, doi. 10.1017/cjn.2020.139

By:

Simon, Sharon L. R.;
Peterson, Anne;
Phillipson, Clark;
Walker, Jonathan M.;
Richmond, Meika;
Jansen, Gerard H.;
Knox, J. David

Publication type:

Article

Creutzfeldt-Jakob disease surveillance in Eastern Slovakia from 2004 to 2016.

Published in:

2018

By:

Feketeová, Eva;
Jarčušková, Dominika;
Janáková, Alžbeta;
Rozprávková, Eva;
Cifráková, Zlatica;
Farkašová-Inaccone, Silvia;
Rimárová, Kvetoslava;
Dorko, Erik;
Gdovinová, Zuzana

Publication type:

journal article

Hepatic Encephalopathy Mimicking Creutzfeldt-Jakob Disease on Laboratory, Physiological, and Imaging Evaluations.

Published in:

American Journal of Case Reports, 2021, v. 22, p. 1, doi. 10.12659/AJCR.932958

By:

Masamune Kimura;
Hideki Kimura;
Hiroki Ishikawa;
Hisayasu Matsuo;
Masahiko Takada;
Koushun Matsuo

Publication type:

Article

Sporadic Creutzfeldt-Jakob disease in adults over 80 years: a 10-year review of United Kingdom surveillance.

Published in:

Age & Ageing, 2024, v. 53, n. 5, p. 1, doi. 10.1093/ageing/afae086

By:

McDermott, Eugene Ace;
Watson, Neil;
Tam, Johnny;
Centola, John;
King, Hatice Kurucu;
Mackenzie, Jan;
Summers, David;
Green, Alison;
Barria, Marcelo A;
Smith, Colin;
Pal, Suvankar

Publication type:

Article

Muhtemel Sporadik Creutzfeldt-Jakob Hastalığı Heidenhain Varyantının Tanısında EEG.

Published in:

Archives of Neuropsychiatry / Nöropsikiyatri Arşivi, 2011, v. 48, n. 1, p. 71, doi. 10.4274/npa.y5540

By:

Akçali, Aylin;
Saygili, Oğuzhan;
Karaoğlan, İlkay;
Neyal, Münife

Publication type:

Article

Late-in-life surgery associated with Creutzfeldt-Jakob disease: a methodological outline for evidence-based guidance.

Published in:

Emerging Themes in Epidemiology, 2013, v. 10, p. 5

By:

Cruz, Mabel;
Mahillo-Fernandez, Ignacio;
Rábano, Alberto;
Siden, Åke;
Calero, Miguel;
Laursen, Henning;
Mølbak, Kåre;
Almazán, Javier;
de Pedro-Cuesta, Jesus

Publication type:

Article