Works matching Prion diseases

Results: 5000

A CONTRIBUIÇÃO GENÉTICA NO DESENVOLVIMENTO DE DOENÇAS PRIÔNICAS: REVISÃO SISTEMÁTICA.

Published in:

Revista Foco (Interdisciplinary Studies Journal), 2023, v. 16, n. 6, p. 1, doi. 10.54751/revistafoco.v16n6-096

By:

Bitu de Freitas, Yuri Borges;
Ribeiro Pimentel, Ana Luiza Machado;
Albuquerque Amorim Ayres, Celina Kalena;
Siqueira Bocchi, Giovanna;
Costa Diniz, Henrique;
Rezende Albernaz, Vítor;
Veloso Correia, Davi;
Costa Alves, Bruna

Publication type:

Article

Lidské prionové nemoci v ČR: 22 let zkušeností Národní referenční laboratoře pro diagnostiku lidských prionových chorob.

Published in:

Neurologie Pro Praxi, 2024, v. 25, n. 1, p. 9, doi. 10.36290/neu.2024.002

By:

Jankovská, Nikol;
Matěj, Radoslav

Publication type:

Article

Toll-like receptor 2 confers partial neuroprotection during prion disease.

Published in:

PLoS ONE, 2018, v. 13, n. 12, p. 1, doi. 10.1371/journal.pone.0208559

By:

Carroll, James A.;
Race, Brent;
Williams, Katie;
Chesebro, Bruce

Publication type:

Article

Seeded Fibrillation as Molecular Basis of the Species Barrier in Human Prion Diseases.

Published in:

PLoS ONE, 2013, v. 8, n. 8, p. 1, doi. 10.1371/journal.pone.0072623

By:

Luers, Lars;
Bannach, Oliver;
Stöhr, Jan;
Wördehoff, Michael Marius;
Wolff, Martin;
Nagel-Steger, Luitgard;
Riesner, Detlev;
Willbold, Dieter;
Birkmann, Eva

Publication type:

Article

Diagnostic accuracy of cerebrospinal fluid biomarkers in genetic prion diseases.

Published in:

2022

By:

Schmitz, Matthias;
Villar-Piqué, Anna;
Hermann, Peter;
Escaramís, Geòrgia;
Calero, Miguel;
Chen, Cao;
Kruse, Niels;
Cramm, Maria;
Golanska, Ewa;
Sikorska, Beata;
Liberski, Pawel P;
Pocchiari, Maurizio;
Lange, Peter;
Stehmann, Christiane;
Sarros, Shannon;
Martí, Eulàlia;
Baldeiras, Inês;
Santana, Isabel;
Žáková, Dana;
Mitrová, Eva

Publication type:

journal article

Chronic wasting disease: Emerging prions and their potential risk.

Published in:

PLoS Pathogens, 2017, v. 13, n. 11, p. 1, doi. 10.1371/journal.ppat.1006619

By:

Hannaoui, Samia;
Schatzl, Hermann M.;
Gilch, Sabine

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

Increased Abundance of M Cells in the Gut Epithelium Dramatically Enhances Oral Prion Disease Susceptibility.

Published in:

PLoS Pathogens, 2016, v. 12, n. 12, p. 1, doi. 10.1371/journal.ppat.1006075

By:

Donaldson, David S.;
Sehgal, Anuj;
Rios, Daniel;
Williams, Ifor R.;
Mabbott, Neil A.

Publication type:

Article

A Single Subcutaneous Injection of Cellulose Ethers Administered Long before Infection Confers Sustained Protection against Prion Diseases in Rodents.

Published in:

PLoS Pathogens, 2016, v. 12, n. 12, p. 1, doi. 10.1371/journal.ppat.1006045

By:

Teruya, Kenta;
Oguma, Ayumi;
Nishizawa, Keiko;
Kawata, Maki;
Sakasegawa, Yuji;
Kamitakahara, Hiroshi;
Doh-ura, Katsumi

Publication type:

Article

Internal consistency, construct validity, and responsiveness of the MRC Prion Disease Rating Scale.

Published in:

Journal of Patient-Reported Outcomes, 2025, v. 9, n. 1, p. 1, doi. 10.1186/s41687-025-00884-3

By:

Leidy, Leah;
Yarlas, Aaron;
Pulido, Robert S.;
Ludwig, Jessica;
Glisic, Kathleen;
Appleby, Brian S.

Publication type:

Article

Epigenetic Changes in Prion and Prion-like Neurodegenerative Diseases: Recent Advances, Potential as Biomarkers, and Future Perspectives.

Published in:

2022

By:

Hernaiz, Adelaida;
Toivonen, Janne Markus;
Bolea, Rosa;
Martín-Burriel, Inmaculada

Publication type:

Literature Review

Humánne priónové ochorenia - „state of the art" 2023.

Published in:

Neurologie Pro Praxi, 2024, v. 25, n. 1, p. 19, doi. 10.36290/neu.2024.005

By:

Kurča, Egon;
Sivák, Štefan;
Skáčik, Pavol

Publication type:

Article

Complement 3+-astrocytes are highly abundant in prion diseases, but their abolishment led to an accelerated disease course and early dysregulation of microglia.

Published in:

Acta Neuropathologica Communications, 2019, v. 7, n. 1, p. N.PAG, doi. 10.1186/s40478-019-0735-1

By:

Hartmann, Kristin;
Sepulveda-Falla, Diego;
Rose, Indigo V. L.;
Madore, Charlotte;
Muth, Christiane;
Matschke, Jakob;
Butovsky, Oleg;
Liddelow, Shane;
Glatzel, Markus;
Krasemann, Susanne

Publication type:

Article

MicroRNA Alterations in the Brain and Body Fluids of Humans and Animal Prion Disease Models: Current Status and Perspectives.

Published in:

Frontiers in Aging Neuroscience, 2018, p. N.PAG, doi. 10.3389/fnagi.2018.00220

By:

Kanata, Eirini;
Thüne, Katrin;
Xanthopoulos, Konstantinos;
Ferrer, Isidre;
Dafou, Dimitra;
Zerr, Inga;
Sklaviadis, Theodoros;
Llorens, Franc

Publication type:

Article

A Preliminary Study for the Determination of Prion Disease for Farm Animals in Ethiopia.

Published in:

Journal of Animal Production / Hayvansal Üretim, 2020, v. 61, n. 1, p. 17, doi. 10.29185/hayuretim.583573

By:

TEFERDEGN, Eden Yitna;
ÜN, Cemal;
TAŞKIN, Turğay

Publication type:

Article

Approaches to therapy against prion diseases focused on the individual defence system.

Published in:

AIMS Molecular Science, 2017, v. 4, n. 3, p. 241, doi. 10.3934/molsci.2017.3.241

By:

Monzón, Marta

Publication type:

Article

Feasibility of Remote Assessment of Human Prion Diseases for Research and Surveillance.

Published in:

Dementia & Geriatric Cognitive Disorders, 2019, v. 47, n. 1/2, p. 79, doi. 10.1159/000497055

By:

Appleby, Brian S.;
Glisic, Kathleen;
Rhoads, Daniel D.;
Bizzi, Alberto;
Cohen, Mark L.;
Mahajan, Supriya

Publication type:

Article

Dysfunction of the PI3 K- Akt- GSK-3 pathway is a common feature in cell culture and in vivo models of prion disease.

Published in:

Neuropathology & Applied Neurobiology, 2014, v. 40, n. 3, p. 311, doi. 10.1111/nan.12066

By:

Simon, D.;
Herva, M. E.;
Benitez, M. J.;
Garrido, J. J.;
Rojo, A. I.;
Cuadrado, A.;
Torres, J. M.;
Wandosell, F.

Publication type:

Article

Phenotypic variability in human prion diseases.

Published in:

Neuropathology & Applied Neurobiology, 2005, v. 31, n. 6, p. 565, doi. 10.1111/j.1365-2990.2005.00697.x

By:

Ironside, J. W.;
Ritchie, D. L.;
Head, M. W.

Publication type:

Article

Ultrastructural pathology of prion diseases revisited: brain biopsy studies.

Published in:

Neuropathology & Applied Neurobiology, 2005, v. 31, n. 1, p. 88, doi. 10.1111/j.1365-2990.2004.00595.x

By:

Liberski, P. P.;
Streichenberger, N.;
Giraud, P.;
Soutrenon, M.;
Meyronnet, D.;
Sikorska, B.;
Kopp, N.

Publication type:

Article

Phenotypic variability in the brains of a family with a prion disease characterized by a 144-base pair insertion in the prion protein gene.

Published in:

Neuropathology & Applied Neurobiology, 2003, v. 29, n. 2, p. 98, doi. 10.1046/j.1365-2990.2003.00423.x

By:

King, A.;
Doey, L.;
Rossor, M.;
Mead, S.;
Collinge, J.;
Lantos, P.

Publication type:

Article

Differential expression of transforming growth factor-β isoforms in human prion diseases.

Published in:

Neuropathology & Applied Neurobiology, 1998, v. 24, n. 4, p. 284, doi. 10.1046/j.1365-2990.1998.00117.x

By:

Tashiro;
Doh-ura;
Iwaki;
Tashiro

Publication type:

Article

Alterations in the brain interactome of the intrinsically disordered N-terminal domain of the cellular prion protein (PrPC) in Alzheimer’s disease.

Published in:

PLoS ONE, 2018, v. 13, n. 5, p. 1, doi. 10.1371/journal.pone.0197659

By:

Ulbrich, Sarah;
Janning, Petra;
Seidel, Ralf;
Matschke, Jakob;
Gonsberg, Anika;
Jung, Sebastian;
Glatzel, Markus;
Engelhard, Martin;
Winklhofer, Konstanze F.;
Tatzelt, Jörg

Publication type:

Article

Innate Immune Tolerance in Microglia Does Not Impact on Central Nervous System Prion Disease.

Published in:

Frontiers in Cellular Neuroscience, 2022, v. 16, p. 1, doi. 10.3389/fncel.2022.918883

By:

Pal, Reiss;
Bradford, Barry M.;
Mabbott, Neil A.

Publication type:

Article

TREM2 supports neuronal protection and microglial reactivity without an effect on misfolded protein deposition in chronic neurodegenerative prion disease.

Published in:

Frontiers in Neuroscience, 2025, p. 1, doi. 10.3389/fnins.2025.1525017

By:

Carpanini, Sarah M.;
Bradford, Barry M.;
Alfieri, Alessio;
Piccardo, Pedro;
Monzón-Sandoval, Jimena;
Brown, Deborah;
Boyle, Aileen;
Pokrovskaya, Aleksandra;
Mabbott, Neil A.;
Manson, Jean;
McColl, Barry W.

Publication type:

Article

Prion Disease: A Tale of Folds and Strains.

Published in:

Brain Pathology, 2013, v. 23, n. 3, p. 321, doi. 10.1111/bpa.12045

By:

Kretzschmar, Hans;
Tatzelt, Jörg

Publication type:

Article

When prion disease Isn't suspected: prion disease as the cause of terminal decline in chronic mixed dementia.

Published in:

2023

By:

Krishnamurthy, Sudarshan;
Harrison, William;
Craft, Suzanne;
Lockhart, Samuel N.;
Bateman, James R.

Publication type:

Case Study

Detection limitations of prion seeding activities in blood samples from patients with sporadic prion disease.

Published in:

BMC Neurology, 2024, v. 24, n. 1, p. 1, doi. 10.1186/s12883-024-03590-7

By:

Nonaka, Toshiaki;
Iwasaki, Yasushi;
Horiuchi, Hiroyuki;
Satoh, Katsuya

Publication type:

Article

Persistent retroviral infection with MoMuLV influences neuropathological signature and phenotype of prion disease.

Published in:

Acta Neuropathologica, 2012, v. 124, n. 1, p. 111, doi. 10.1007/s00401-012-0944-1

By:

Krasemann, Susanne;
Neumann, Melanie;
Luepke, Jan-Paul;
Grashorn, Juliane;
Wurr, Steffanie;
Stocking, Carol;
Glatzel, Markus

Publication type:

Article

Phenotypic variability of sporadic human prion disease and its molecular basis: past, present, and future.

Published in:

Acta Neuropathologica, 2011, v. 121, n. 1, p. 91, doi. 10.1007/s00401-010-0779-6

By:

Parchi, Piero;
Strammiello, Rosaria;
Giese, Armin;
Kretzschmar, Hans

Publication type:

Article

Recombinant prion protein induces a new transmissible prion disease in wild-type animals.

Published in:

Acta Neuropathologica, 2010, v. 119, n. 2, p. 177, doi. 10.1007/s00401-009-0633-x

By:

Makarava, Natallia;
Kovacs, Gabor G.;
Bocharova, Olga;
Savtchenko, Regina;
Alexeeva, Irina;
Budka, Herbert;
Rohwer, Robert G.;
Baskakov, Ilia V.

Publication type:

Article

Distribution of intraneuronal immunoreactivity for the prion protein in human prion diseases.

Published in:

Acta Neuropathologica, 2002, v. 104, n. 3, p. 320, doi. 10.1007/s00401-002-0550-8

By:

Kovacs, Gabor G.;
Voigtländer, Till;
Hainfellner, Johannes A.;
Budka, Herbert

Publication type:

Article

Deposition patterns of disease-associated prion protein in captive mule deer brains with chronic wasting disease.

Published in:

Acta Neuropathologica, 2001, v. 102, n. 5, p. 496, doi. 10.1007/s004010100417

By:

Liberski, Pawel P.;
Guiroy, Don C.;
Williams, Elizabeth S.;
Walis, Anna;
Budka, Herbert

Publication type:

Article

Prion disease in Indigenous Australians.

Published in:

Internal Medicine Journal, 2021, v. 51, n. 7, p. 1101, doi. 10.1111/imj.14835

By:

Panegyres, Peter K.;
Stehmann, Christiane;
Klug, Genevieve M.;
Masters, Colin L.;
Collins, Steven

Publication type:

Article

The degree of astrocyte activation is predictive of the incubation time to prion disease.

Published in:

Acta Neuropathologica Communications, 2021, v. 9, n. 1, p. 1, doi. 10.1186/s40478-021-01192-9

By:

Makarava, Natallia;
Mychko, Olga;
Chang, Jennifer Chen-Yu;
Molesworth, Kara;
Baskakov, Ilia V.

Publication type:

Article

Non-cell autonomous astrocyte-mediated neuronal toxicity in prion diseases.

Published in:

Acta Neuropathologica Communications, 2021, v. 9, n. 1, p. 1, doi. 10.1186/s40478-021-01123-8

By:

Kushwaha, Rajesh;
Sinha, Anshuman;
Makarava, Natallia;
Molesworth, Kara;
Baskakov, Ilia V.

Publication type:

Article

Interactions between Cytokines and the Pathogenesis of Prion Diseases: Insights and Implications.

Published in:

Brain Sciences (2076-3425), 2024, v. 14, n. 5, p. 413, doi. 10.3390/brainsci14050413

By:

Assis-de-Lemos, Gabriela;
Moura-do-Nascimento, Rayanne;
Amaral-do-Nascimento, Manuela;
Miceli, Ana C.;
Vieira, Tuane C. R. G.

Publication type:

Article

Plasma total prion protein as a potential biomarker for neurodegenerative dementia: diagnostic accuracy in the spectrum of prion diseases.

Published in:

Neuropathology & Applied Neurobiology, 2020, v. 46, n. 3, p. 240, doi. 10.1111/nan.12573

By:

Llorens, F.;
Villar‐Piqué, A.;
Schmitz, M.;
Diaz‐Lucena, D.;
Wohlhage, M.;
Hermann, P.;
Goebel, S.;
Schmidt, I.;
Glatzel, M.;
Hauw, J.‐J.;
Sikorska, B.;
Liberski, P. P.;
Riggert, J.;
Ferrer, I.;
Zerr, I.

Publication type:

Article

PrPST, a Soluble, Protease Resistant and Truncated PrP Form Features in the Pathogenesis of a Genetic Prion Disease.

Published in:

PLoS ONE, 2013, v. 8, n. 7, p. 1, doi. 10.1371/journal.pone.0069583

By:

Friedman-Levi, Yael;
Mizrahi, Michal;
Frid, Kati;
Binyamin, Orli;
Gabizon, Ruth

Publication type:

Article

Analyses of the Survival Time and the Influencing Factors of Chinese Patients with Prion Diseases Based on the Surveillance Data from 2008–2011

Published in:

PLoS ONE, 2013, v. 8, n. 5, p. 1, doi. 10.1371/journal.pone.0062553

By:

Chen, Cao;
Wang, Ji-Chun;
Shi, Qi;
Zhou, Wei;
Zhang, Xiao-Mei;
Zhang, Jin;
Tian, Chan;
Gao, Chen;
Dong, Xiao-Ping

Publication type:

Article

Multifaceted Role of Sialylation in Prion Diseases.

Published in:

Frontiers in Neuroscience, 2016, p. 1, doi. 10.3389/fnins.2016.00358

By:

Baskakov, Ilia V.;
Katorcha, Elizaveta;
Ledesma, Maria Dolores;
Schmitt-Ulms, Gerold

Publication type:

Article

Multifaceted Role of Sialylation in Prion Diseases.

Published in:

Frontiers in Neuroscience, 2016, p. 1, doi. 10.3389/fnins.2016.00358

By:

Baskakov, Ilia V.;
Katorcha, Elizaveta

Publication type:

Article

Validation of the Medical Research Council prion disease rating scale in France.

Published in:

Brain Communications, 2023, v. 5, n. 6, p. 1, doi. 10.1093/braincomms/fcad267

By:

Brandel, Jean-Philippe;
Welaratne, Arlette;
Denouel, Angeline;
Haïk, Stéphane

Publication type:

Article

Downregulation of STAT3 transcription factor reverses synaptotoxic phenotype of reactive astrocytes associated with prion diseases.

Published in:

Acta Neuropathologica Communications, 2025, v. 13, n. 1, p. 1, doi. 10.1186/s40478-025-02028-6

By:

Kushwaha, Rajesh;
Molesworth, Kara;
Makarava, Natallia;
Baskakov, Ilia V.

Publication type:

Article

The Braak hypothesis in prion disease with a focus on Creutzfeldt–Jakob disease.

Published in:

Neuropathology, 2020, v. 40, n. 5, p. 436, doi. 10.1111/neup.12654

By:

Iwasaki, Yasushi

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

Prion protein E219K polymorphism: from the discovery of the KANNO blood group to interventions for human prion disease.

Published in:

Frontiers in Neurology, 2024, p. 01, doi. 10.3389/fneur.2024.1392984

By:

Si-Si Wang;
Zhao-Li Meng;
Yi-Wen Zhang;
Yi-Shuang Yan;
Ling-Bo Li

Publication type:

Article

Enfermedades priónicas: historia, diversidad e importancia socioeconómica como paradigma de las Enfermedades Raras.

Published in:

Araucaria, 2021, v. 23, n. 46, p. 429, doi. 10.12795/araucaria.2021.i46.21

By:

Charco, Jorge M.;
Barrio, Tomás;
Eraña, Hasier

Publication type:

Article

Insight From Animals Resistant to Prion Diseases: Deciphering the Genotype – Morphotype – Phenotype Code for the Prion Protein.

Published in:

Frontiers in Cellular Neuroscience, 2020, v. 14, p. N.PAG, doi. 10.3389/fncel.2020.00254

By:

Myers, Ryan;
Cembran, Alessandro;
Fernandez-Funez, Pedro

Publication type:

Article

Cognitive decline heralds onset of symptomatic inherited prion disease.

Published in:

2021

By:

Mole, Joseph;
Mead, Simon;
Rudge, Peter;
Nihat, Akin;
Mok, Tzehow;
Collinge, John;
Caine, Diana

Publication type:

journal article