Results 151 to 160 of about 42,402 (225)

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

J Patient Rep Outcomes
Leidy L, Yarlas A, Pulido RS, Ludwig J, Glisic K, Appleby BS.   +5 more
europepmc   +1 more source

Development of a user guide to support administration of the MRC Prion Disease Rating Scale in research and clinical settings for prion diseases. [PDF]

Prion
Pulido RS, Marshall C, Smith AV, Edge H, Yarlas A, Appleby B, Brandel JP, Collins S, Omer N, Zerr I, Mead S.   +10 more
europepmc   +1 more source

Overexpression of bank vole PrP(I109) in mice induces a spontaneous atypical prion disease with sex-dependent onset, early NfL elevation, and universal prion strain permissiveness. [PDF]

Acta Neuropathol Commun
Eraña H, Vidal E, Fernández-Borges N, Charco JM, Díaz-Domínguez CM, Sampedro-Torres-Quevedo C, San-Juan-Ansoleaga M, Fernández-Muñoz E, Galarza-Ahumada J, Pérez-Castro MÁ, Gonçalves-Anjo N, Piñeiro P, Pirisinu L, Di Bari MA, Giler S, Raimondi I, Espinosa JC, Vanni I, D'Agostino C, Rodríguez-Cuesta J, Pasetto L, Bonetto V, González-Martín N, Teijeira S, Zou WQ, Geijo M, Torres JM, Chiesa R, Sánchez-Martín MA, Nonno R, Requena JR, Castilla J.   +31 more
europepmc   +1 more source

FDG-PET patterns associate with survival in patients with prion disease. [PDF]

Ann Clin Transl Neurol
Corriveau-Lecavalier N, Piura YD, Appleby BS, Shir D, Barnard LR, Gogineni V, Jones DT, Day GS.   +7 more
europepmc   +1 more source

Limbic system synaptic dysfunctions associated with prion disease onset. [PDF]

Acta Neuropathol Commun
Foliaki ST, Groveman BR, Dews EA, Williams K, El Soufi H, Schwarz B, Leung JM, Schneider CA, Schwartz CL, Bohrnsen E, Kimzey CD, Race B, Haigh CL.   +12 more
europepmc   +1 more source

Inherited prion disease caused by a novel frameshift mutation of <i>PRNP</i> resulting in protein truncation at codon 157. [PDF]

J Alzheimers Dis
Holm-Mercer L, Mok TH, Sequeira D, Coysh T, Rudge P, Ramadan H, Darwent L, Campbell T, Murphy T, Smith C, Ritchie D, Brandner S, Jaunmuktane Z, Collinge J, Mead S.   +14 more
europepmc   +1 more source

Prion Protein Endoproteolysis: Cleavage Sites, Mechanisms and Connections to Prion Disease. [PDF]

J Neurochem
Castle AR, Westaway D.
europepmc   +1 more source

PRNP E146G mutation inherited prion disease: distinctive clinical, pathological and fluid biomarker features. [PDF]

J Neurol
Coysh T, Jaunmuktane Z, Hosszu LLP, Majbour N, Zhang F, Campbell T, Darwent L, Matus MB, Chan E, Holm-Mercer L, Mok TH, Wadsworth JDF, Bieschke J, Nithi K, Brandner S, Smith C, Esiri M, Collinge J, Mead S.   +18 more
europepmc   +1 more source

Therapeutic effects of adipose-derived mesenchymal stem cells combined with glymphatic system activation in prion disease. [PDF]

Mol Neurodegener
Zayed M, Kim YC, Jeong BH.
europepmc   +1 more source

In vivo base editing extends lifespan of a humanized mouse model of prion disease. [PDF]

Nat Med
An M, Davis JR, Levy JM, Serack FE, Harvey JW, Brauer PP, Pirtle CP, Berríos KN, Newby GA, Yeh WH, Kamath N, Mortberg M, Lian Y, Howard M, DeSouza-Lenz K, Guzman K, Thai A, Graffam S, Laversenne V, Coffey AA, Frei J, Pierce SE, Safar JG, Deverman BE, Minikel EV, Vallabh SM, Liu DR.   +26 more
europepmc   +1 more source