Detalhe da pesquisa
1.
The role of environmental factors on sporadic Creutzfeldt-Jakob disease mortality: evidence from an age-period-cohort analysis.
Eur J Epidemiol
; 38(7): 757-764, 2023 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-37191829
2.
Prospective 25-year surveillance of prion diseases in France, 1992 to 2016: a slow waning of epidemics and an increase in observed sporadic forms.
Euro Surveill
; 28(50)2023 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-38099349
3.
An in vivo Caenorhabditis elegans model for therapeutic research in human prion diseases.
Brain
; 144(9): 2745-2758, 2021 10 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-34687213
4.
Factors Influencing the Incubation of an Infectious Form of Creutzfeldt-Jakob Disease.
Clin Infect Dis
; 70(7): 1487-1490, 2020 03 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-31351441
5.
Examining the Reserve Hypothesis in Parkinson's Disease: A Longitudinal Study.
Mov Disord
; 34(11): 1663-1671, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31518456
6.
Region-specific protein misfolding cyclic amplification reproduces brain tropism of prion strains.
J Biol Chem
; 292(40): 16688-16696, 2017 10 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28821618
7.
Variant Creutzfeldt-Jakob Disease Diagnosed 7.5 Years after Occupational Exposure.
N Engl J Med
; 383(1): 83-85, 2020 07 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32609989
8.
Neuropathology of iatrogenic Creutzfeldt-Jakob disease and immunoassay of French cadaver-sourced growth hormone batches suggest possible transmission of tauopathy and long incubation periods for the transmission of Abeta pathology.
Acta Neuropathol
; 135(2): 201-212, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29209767
9.
Prions in the urine of patients with variant Creutzfeldt-Jakob disease.
N Engl J Med
; 371(6): 530-9, 2014 Aug 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-25099577
10.
Accuracy of diagnosis criteria in patients with suspected diagnosis of sporadic Creutzfeldt-Jakob disease and detection of 14-3-3 protein, France, 1992 to 2009.
Euro Surveill
; 22(41)2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-29043964
11.
Case report of Lewy body disease mimicking Creutzfeldt-Jakob disease in a 44-year-old man.
BMC Neurol
; 16: 122, 2016 Jul 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-27475058
12.
History of Prions and transmission of protein misfolding.
Bull Acad Natl Med
; 199(6): 787-796, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-29901879
13.
Cycline efficacy on the propagation of human prions in primary cultured neurons is strain-specific.
J Infect Dis
; 209(7): 1144-8, 2014 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24265435
14.
Substitutions at residue 211 in the prion protein drive a switch between CJD and GSS syndrome, a new mechanism governing inherited neurodegenerative disorders.
Hum Mol Genet
; 21(26): 5417-28, 2012 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22965875
15.
Intensity of human prion disease surveillance predicts observed disease incidence.
J Neurol Neurosurg Psychiatry
; 84(12): 1372-7, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-23965290
16.
Validation of the Medical Research Council prion disease rating scale in France.
Brain Commun
; 5(6): fcad267, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37953837
17.
Assessment of axial rotation movement in cervical dystonia using cone-beam computed tomography.
Clin Biomech (Bristol, Avon)
; 107: 106037, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37429102
18.
Constant transmission properties of variant Creutzfeldt-Jakob disease in 5 countries.
Emerg Infect Dis
; 18(10): 1574-9, 2012 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23017202
19.
Iatrogenic Creutzfeldt-Jakob disease, final assessment.
Emerg Infect Dis
; 18(6): 901-7, 2012 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22607808
20.
Preclinical sporadic Creutzfeldt-Jakob disease in French blood donors: an epidemiologic model-based study.
Transfusion
; 52(6): 1290-5, 2012 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22128904