Works matching Creutzfeldt-Jakob disease (CJD)

Results: 931

RARB and STMN2 polymorphisms are not associated with sporadic Creutzfeldt-Jakob disease (CJD) in the Korean population.

Published in:

Molecular Biology Reports, 2014, v. 41, n. 4, p. 2389, doi. 10.1007/s11033-014-3093-x

By:

Jeong, Byung-Hoon;
Kim, Hae-Jung;
Lee, Kyung-Hee;
Carp, Richard;
Kim, Yong-Sun

Publication type:

Article

Rare cause of rapidly progressive dementia - Creutzfeldt-Jakob disease (CJD) with negative 14-3-3 protein - Case Report.

Published in:

2019

By:

Bąk, Marcin;
Jamroz-Wiśniewska, Anna;
Nowakowska, Małgorzata;
Ciesielka, Marcin;
Sałek, Magdalena;
Rawska, Aleksandra;
Rejdak, Konrad

Publication type:

Case Study

The Creutzfeldt-Jakob disease (CJD) neurological status scale: a new tool for evaluation of disease severity and progression.

Published in:

Acta Neurologica Scandinavica, 2011, v. 124, n. 6, p. 368, doi. 10.1111/j.1600-0404.2011.01489.x

By:

Cohen, O. S.;
Prohovnik, I.;
Korczyn, A. D.;
Ephraty, L.;
Nitsan, Z.;
Tsabari, R.;
Appel, S.;
Rosenmann, H.;
Kahana, E.;
Chapman, J.

Publication type:

Article

The role of stress and anxiety in the onset of familial Creutzfeldt-Jakob Disease (CJD): Review.

Published in:

Stress: The International Journal on the Biology of Stress, 2009, v. 12, n. 5, p. 371, doi. 10.1080/10253890802508520

By:

Gigi, Ariela

Publication type:

Article

Elevated E200K Somatic Mutation of the Prion Protein Gene (PRNP) in the Brain Tissues of Patients with Sporadic Creutzfeldt–Jakob Disease (CJD).

Published in:

International Journal of Molecular Sciences, 2023, v. 24, n. 19, p. 14831, doi. 10.3390/ijms241914831

By:

Won, Sae-Young;
Kim, Yong-Chan;
Jeong, Byung-Hoon

Publication type:

Article

Correction: The natural history study of preclinical genetic Creutzfeldt-Jakob Disease (CJD): a prospective longitudinal study protocol.

Published in:

2023

By:

Bregman, Noa;
Shiner, Tamara;
Kavé, Gitit;
Alcalay, Roy;
Gana-Weisz, Mali;
Goldstein, Orly;
Glinka, Tal;
Aizenstein, Orna;
Ben Bashat, Dafna;
Alcalay, Yifat;
Mirelman, Anat;
Thaler, Avner;
Giladi, Nir;
Omer, Nurit

Publication type:

Correction Notice

The natural history study of preclinical genetic Creutzfeldt-Jakob Disease (CJD): a prospective longitudinal study protocol.

Published in:

BMC Neurology, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12883-023-03193-8

By:

Bregman, Noa;
Shiner, Tamara;
Kavé, Gitit;
Alcalay, Roy;
Gana-Weisz, Mali;
Goldstein, Orly;
Glinka, Tal;
Aizenstein, Orna;
Bashat, Dafna Ben;
Alcalay, Yifat;
Mirelman, Anat;
Thaler, Avner;
Giladi, Nir;
Omer, Nurit

Publication type:

Article

The natural history study of preclinical genetic Creutzfeldt-Jakob Disease (CJD): a prospective longitudinal study protocol.

Published in:

BMC Neurology, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12883-023-03193-8

By:

Noa, Bregman;
Tamara, Shiner;
Gitit, Kavé;
Roy, Alcalay;
Mali, Gana-Weisz;
Orly, Goldstein;
Tal, Glinka;
Orna, Aizenstein;
Dafna, Ben Bashat;
Yifat, Alcalay;
Anat, Mirelman;
Avner, Thaler;
Nir, Giladi;
Nurit, Omer

Publication type:

Article

The Role of Social Work in Supporting People Affected by Creutzfeldt–Jakob Disease (CJD): A Scoping Review.

Published in:

British Journal of Social Work, 2019, v. 49, n. 7, p. 1798, doi. 10.1093/bjsw/bcy116

By:

Manthorpe, Jill;
Simcock, Peter

Publication type:

Article

Immunohistochemical studies of the PrP[sup CJD] deposition in Creutzfeldt-Jakob disease.

Published in:

Neuropathology, 2000, v. 20, n. 2, p. 124, doi. 10.1046/j.1440-1789.2000.00285.x

By:

Tanaka, S.;
Saito, M.;
Morimatsu, M.;
Ohama, E.

Publication type:

Article

The first report of RPSA polymorphisms, also called 37/67 kDa LRP/LR gene, in sporadic Creutzfeldt-Jakob disease (CJD).

Published in:: BMC Medical Genetics, 2011, v. 12, n. 1, p. 108, doi. 10.1186/1471-2350-12-108
Publication type:: Article

Lack of association between 14-3-3 beta gene ( YWHAB) polymorphisms and sporadic Creutzfeldt-Jakob disease (CJD).

Published in:

Molecular Biology Reports, 2012, v. 39, n. 12, p. 10647, doi. 10.1007/s11033-012-1954-8

By:

Jeong, Byung-Hoon;
Jin, Hyoung-Tae;
Choi, Eun-Kyoung;
Carp, Richard;
Kim, Yong-Sun

Publication type:

Article

A Contemporary Risk Analysis of Iatrogenic Transmission of Creutzfeldt-Jakob Disease (CJD) via Corneal Transplantation in the United States.

Published in:

Ophthalmology & Therapy, 2020, v. 9, n. 3, p. 465, doi. 10.1007/s40123-020-00272-8

By:

Martheswaran, Tanisha;
Desautels, Jordan D.;
Moshirfar, Majid;
Shmunes, Kathryn M.;
Ronquillo, Yasmyne C.;
Hoopes, Phillip C.

Publication type:

Article

Implications for Creutzfeldt-Jakob Disease (CJD) in Dentistry: a Review of Current Knowledge.

Published in:

Journal of Dental Research, 2008, v. 87, n. 6, p. 511, doi. 10.1177/154405910808700613

By:

Walker, J. T.;
Dickinson, J.;
Sutton, J. M.;
Marsh, P. D.;
Raven, N. D. H.

Publication type:

Article

Counselling people with Creutzfeldt-Jakob Disease (CJD) and their families.

Published in:

2010

By:

Morris C

Publication type:

Journal Article

Neuronal expression of phosphorylated RNA-dependent protein kinase (pkr) in Creutzfeldt-Jakob Disease (CJD).

Published in:: Clinical Neuropathology, 2008, v. 27, n. 3, p. 160
Publication type:: Article

A polymorphism in the YWHAH gene encoding 14-3-3 eta that is not associated with sporadic Creutzfeldt-Jakob disease (CJD).

Published in:

Molecular Biology Reports, 2012, v. 39, n. 4, p. 3619, doi. 10.1007/s11033-011-1136-0

By:

Yun, Jisuk;
Jeong, Byung-Hoon;
Kim, Hae-Jung;
Park, Young-Jae;
Lee, Yun-Jung;
Choi, Eun-Kyoung;
Carp, Richard;
Kim, Yong-Sun

Publication type:

Article

PrP<sup>res</sup> deposition in the retina is a common finding of sporadic, familial and iatrogenic Creutzfeldt-Jakob diseases (CJD).

Published in:

2018

By:

Takao, Masaki;
Kimura, Hiroaki;
Kitamoto, Tetsuyuki;
Mihara, Ban

Publication type:

Letter

Creutzfeldt-Jakob disease (CJD) and assisted reproductive technology (ART). Quantification of risks as part of informed consent.

Published in:

1998

By:

Kemmann, E

Publication type:

journal article

Debate. Creutzfeldt-Jakob disease (CJD) and assisted reproductive technology (ART). Quantification of risks as part of informed consent.

Published in:

Human Reproduction, 1998, v. 13, n. 7, p. 1777, doi. 10.1093/humrep/13.7.1777

By:

Kemmann, E

Publication type:

Article

Familial Creutzfeldt--Jakob Disease (CJD) Kindred -- An Unusual Case Report from India.

Published in:

2024

By:

Sharma, Bhawna;
Chiddarwar, Deepali;
Sharma, Pankaj Kumar;
Gupta, Ashish;
Sharma, Pranjal

Publication type:

Case Study

A case of V180I genetic mutation Creutzfeldt Jakob disease (CJD) with delusional misidentification as an initial symptom.

Published in:

2022

By:

Nagata, Tomoyuki;
Shinagawa, Shunichiro;
Kobayashi, Nobuyuki;
Kondo, Kazuhiro;
Shigeta, Masahiro

Publication type:

Report

P.220: Decoding differences in the replication of sporadic and variant Creutzfeldt-Jakob disease (CJD) in transgenic mice over-expressing human prion protein (TgRM).

Published in:

Prion, 2014, v. 8, p. 131

By:

Yakovleva, Oksana;
Saá, Paula;
Piccardo, Pedro;
de Castro, Jorge;
Vasilyeva, Irina;
Cervenak, Anton;
Cervenakova, Larisa

Publication type:

Article

P.209: Diagnostic value of surrogate cerebrospinal fluid biomarkers for the clinical diagnosis of Creutzfeldt-Jakob disease: A 10-year review from a CJD referral laboratory.

Published in:

Prion, 2014, v. 8, p. 125

By:

Poaaiolini, Ilaria;
Capellari, Sabina;
Ladogana, Anna;
McGuire, Lynne l.;
Green, Alison J. E.;
Pocchiari, Maurizio;
Parchi, Piero

Publication type:

Article

Neuropathological Diagnostic Criteria for Creutzfeldt-Jakob Disease (CJD) and Other Human Spongiform Encephalopathies (Prion Diseases).

Published in:

Brain Pathology, 1995, v. 5, n. 4, p. 459, doi. 10.1111/j.1750-3639.1995.tb00625.x

By:

Budka, Herbert;
Aguzzi, Adriano;
Brown, Paul;
Brucher, Jean-Marie;
Bugiani, Orso;
Gullotta, Filippo;
Haltia, Matti;
Hauw, Jean-Jacques;
Ironside, James W.;
Jellinger, Kurt;
Kretzschmar, Hans A.;
Lantos, Peter L.;
Masullo, Carlo;
Schlote, Wolfgang;
Tateishi, Jun;
Weller, Roy O.

Publication type:

Article

Tissue Handling in Suspected Creutzfeldt-Jakob Disease (CJD) and Other Human Spongiform Encephalopathies (Prion Diseases).

Published in:

Brain Pathology, 1995, v. 5, n. 3, p. 319, doi. 10.1111/j.1750-3639.1995.tb00609.x

By:

Budka, Herbert;
Aguzzi, Adriano;
Brown, Paul;
Brucher, Jean-Marie;
Bugiani, Orso;
Collinge, John;
Diringer, Heino;
Gullotta, Filippo;
Haltia, Matti;
Hauw, Jean-Jacques;
Ironside, James W.;
Kretzschmar, Hans A.;
Lantos, Peter L.;
Masullo, Carlo;
Pocchiari, Maurizio;
Schlote, Wolfgang;
Tateishi, Jun;
Will, Robert G.

Publication type:

Article

Positron emission tomography with [<sup>18</sup>F]FDG in the diagnosis of Creutzfeldt-Jakob disease (CJD).

Published in:

Journal of Neurology, 2002, v. 249, n. 6, p. 699, doi. 10.1007/s00415-002-0695-3

By:

Henkel, Karsten;
Zerr, Inga;
Hertel, Andreas;
Gratz, Klaus-F.;
Schröter, Andreas;
Tschampa, Henriette J.;
Bihl, Heiner;
Büll, Udalrich;
Grünwald, Frank;
Drzezga, Alexander;
Spitz, Jürg;
Poser, Sigrid

Publication type:

Article

The Various Faces of Creutzfeldt-Jakob Disease (CJD); a Case of CJD Presenting as Psychosis in a Middle-Aged Woman.

Published in:

2022

By:

Sodiya, Olusegun;
Odutola, Akinkunmi;
Hakeem, Michel

Publication type:

Abstract

Creutzfeldt‐Jakob Disease (CJD): Time from Symptom Onset Until Subnormal Magnetic Resonance Imaging (MRI) of brain.

Published in:

Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.064992

By:

Shergelashvili, Tea;
Chabrashvili, Tinatin

Publication type:

Article

O1-04-03: Creutzfeldt-Jakob Disease (CJD) surveillance in Japan: Two distinct subtypes of CJD associated with cadaveric dura mater graft and the first Japanese case of variant CJD

Published in:

2006

By:

Yamada, Masahito;
Shinohara-Noguchi, Moeko;
Hamaguchi, Tsuyoshi;
Nakamura, Yosikazu;
Kitamoto, Tetsuyuki;
Sato, Takeshi;
Mizusawa, Hidehiro

Publication type:

Abstract

O1-04-03: Creutzfeldt-Jakob Disease (CJD) surveillance in Japan: Two distinct subtypes of CJD associated with cadaveric dura mater graft and the first Japanese case of variant CJD

Published in:

2006

By:

Yamada, Masahito;
Shinohara-Noguchi, Moeko;
Hamaguchi, Tsuyoshi;
Nakamura, Yosikazu;
Kitamoto, Tetsuyuki;
Sato, Takeshi;
Mizusawa, Hidehiro

Publication type:

Abstract

Parkinsonism as an initial presentation of Creutzfeldt‐Jakob disease: A case report and review of literature.

Published in:

2024

By:

Bahrami, Sahar Nikkhah;
Karimi, Asal Sadat;
Khosravi, Sepehr;
Almasi‐Dooghaee, Mostafa

Publication type:

Case Study

Transmission of Creutzfeldt-Jakob Disease to the Patas Monkey (Erythrocebus patas) with Cytopathological Changes in in vitro Cultivated Brain Cells.

Published in:

Intervirology, 1975, v. 6, n. 3, p. 150, doi. 10.1159/000149467

By:

Espana, Carlos;
Gajdusek, Carleton;
Gibbs, jr., Clarence J.;
Lock, Katńerine

Publication type:

Article

Cases of Creutzfeldt-Jakob disease in young individuals: open questions regarding aetiology.

Published in:

Frontiers in Cellular Neuroscience, 2025, p. 1, doi. 10.3389/fncel.2025.1571662

By:

Baskakov, Ilia V.

Publication type:

Article

Case report: Atypical young case of MV1 Creutzfeldt-Jakob disease with unusually long survival.

Published in:

Frontiers in Cellular Neuroscience, 2025, p. 1, doi. 10.3389/fncel.2024.1518542

By:

Ahn, Lucie Yeongran;
Cohen, Mark L.;
Cali, Ignazio;
Russell, Tia;
Ludwig, Jessica;
Jia, Xun;
Bizzi, Alberto;
Schonberger, Lawrence B.;
Maddox, Ryan A.;
Paul, Rohini;
Ghazarian, Tania C.;
Garcha, Jaspreet;
Hammoudi, Mostafa;
Appleby, Brian Stephen

Publication type:

Article

An atypical phenotype of CJD associated with the E200K mutation in the prion protein gene.

Published in:

Neurological Sciences, 2010, v. 31, n. 6, p. 837, doi. 10.1007/s10072-010-0388-0

By:

Masullo, Carlo;
Bizzarro, Alessandra;
Guglielmi, Valeria;
Iannaccone, Elisabetta;
Minicuci, Giacomo;
Vita, Maria Gabriella;
Capellari, Sabina;
Parchi, Piero;
Servidei, Serenella

Publication type:

Article

Elevation of neuron‐specific enolase in serum and cerebrospinal fluid of early stage Creutzfeldt–Jakob disease.

Published in:

Acta Neurologica Scandinavica, 2000, v. 102, n. 6, p. 385, doi. 10.1034/j.1600-0404.2000.102006385.x

By:

Kohira, I.;
Tsuji, T.;
Ishizu, H.;
Takao, Y.;
Wake, A.;
Abe, K.;
Kuroda, S.

Publication type:

Article

Prion Mutations in Republic of Republic of Korea, China, and Japan.

Published in:

2023

By:

Kim, Dan Yeong;
Shim, Kyu Hwan;
Bagyinszky, Eva;
An, Seong Soo A.

Publication type:

Literature Review

Neuronal and astrocytic responses involving the serotonergic system in human spongiform encephalopathies.

Published in:

Neuropathology & Applied Neurobiology, 2003, v. 29, n. 5, p. 482, doi. 10.1046/j.1365-2990.2003.00486.x

By:

Fraser, E.;
McDonagh, A.M.;
Head, M.;
Bishop, M.;
Ironside, J.W.;
Mann, D.M.A.

Publication type:

Article

The allograft inflammatory factor-1 in Creutzfeldt–Jakob disease brains.

Published in:

Neuropathology & Applied Neurobiology, 2003, v. 29, n. 4, p. 389, doi. 10.1046/j.1365-2990.2003.00476.x

By:

Deininger, M. H.;
Weinschenk, T.;
Meyermann, R.;
Schluesener, H. J.

Publication type:

Article

Prion disease with a 144 base pair insertion: unusual cerebellar prion protein immunoreactivity.

Published in:

Acta Neuropathologica, 2005, v. 110, n. 5, p. 513, doi. 10.1007/s00401-005-1073-x

By:

Gelpi, Ellen;
Kovacs, Gabor G.;
Ströbel, Thomas;
Koperek, Oskar;
Voigtländer, Till;
Liberski, Pawel P.;
Budka, Herbert

Publication type:

Article

Development of an Ultra-Rapid Diagnostic Method Based on Heart-Type Fatty Acid Binding Protein Levels in the CSF of CJD Patients.

Published in:

Cellular & Molecular Neurobiology, 2010, v. 30, n. 7, p. 991, doi. 10.1007/s10571-010-9529-5

By:

Matsui, Yuki;
Satoh, Katsuya;
Mutsukura, Kazuo;
Watanabe, Takuya;
Nishida, Noriyuki;
Matsuda, Hideo;
Sugino, Masaichi;
Shirabe, Susumu;
Eguchi, Katsumi;
Kataoka, Yasufumi

Publication type:

Article

Case Report: A Case of Creutzfeldt–Jakob Heidenhain Variant Simulating PRES.

Published in:

Diagnostics (2075-4418), 2022, v. 12, n. 7, p. N.PAG, doi. 10.3390/diagnostics12071558

By:

Antonioni, Annibale;
Raho, Emanuela Maria;
Gozzi, Andrea;
Cotta Ramusino, Niccolò;
Cesnik, Edward;
Padroni, Marina;
De Vito, Alessandro;
Pugliatti, Maura;
Tugnoli, Valeria

Publication type:

Article

Further Characterization of Glycoform-Selective Prions of Variably Protease-Sensitive Prionopathy.

Published in:

Pathogens, 2021, v. 10, n. 5, p. 513, doi. 10.3390/pathogens10050513

By:

Zhang, Weiguanliu;
Xiao, Xiangzhu;
Ding, Mingxuan;
Yuan, Jue;
Foutz, Aaron;
Moudjou, Mohammed;
Kitamoto, Tetsuyuki;
Langeveld, Jan P. M.;
Cui, Li;
Zou, Wen-Quan;
Young, Lawrence S.

Publication type:

Article

Comparison of cerebrospinal fluid tau, ptau(181), synuclein, and 14-3-3 for the detection of Creutzfeldt–Jakob disease in clinical practice.

Published in:

Journal of Neural Transmission, 2022, v. 129, n. 2, p. 133, doi. 10.1007/s00702-021-02443-8

By:

Fayolle, Martin;
Lehmann, Sylvain;
Delaby, Constance

Publication type:

Article

Clinical Use of Improved Diagnostic Testing for Detection of Prion Disease.

Published in:

Viruses (1999-4915), 2021, v. 13, n. 5, p. 789, doi. 10.3390/v13050789

By:

Figgie Jr., Mark P.;
Appleby, Brian S.;
Caughey, Byron

Publication type:

Article

Tumor frontal, trastorno afectivo y encefalopatía. Discusión del caso clínico presentado en el volumen 6, número 2.

Published in:

Revista Ciencias de la Salud, 2009, v. 7, n. 1, p. 100

By:

Hurtado, Fernando Velandia;
Cardozo, Juan Pablo Salgado

Publication type:

Article

An autopsy case of MV 2K + C subtype of Creutzfeldt–Jakob disease.

Published in:

Neuropathology, 2024, v. 44, n. 4, p. 304, doi. 10.1111/neup.12964

By:

Uchino, Akiko;
Saito, Yuko;
Tokuda, Sho;
Saburo, Yagishita;
Murayama, Shigeo;
Hasegawa, Kazuko

Publication type:

Article

Continuous intraventricular infusion of pentosan polysulfate: Clinical trial against prion diseases.

Published in:

Neuropathology, 2009, v. 29, n. 5, p. 632, doi. 10.1111/j.1440-1789.2009.01058.x

By:

Tsuboi, Yoshio;
Doh-ura, Katsumi;
Yamada, Tatsuo

Publication type:

Article

Miliary brain metastases presenting as rapidly progressive dementia.

Published in:

Neuropathology, 2005, v. 25, n. 2, p. 153, doi. 10.1111/j.1440-1789.2005.00595.x

By:

Rivas, Eloy;
Sanchez-Herrero, Joaquin;
Alonso, Miguel;
Alvarez, Maria J.;
Teijeira, Susana;
Ballestín, Claudio;
Tardio, Antoni;
Navarro, Carmen

Publication type:

Article