Detalhe da pesquisa
1.
A point mutation in GPI-attachment signal peptide accelerates the development of prion disease.
Acta Neuropathol
; 145(5): 637-650, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36879070
2.
An autopsy case of variably protease-sensitive prionopathy with Met/Met homogeneity at codon 129.
Neuropathology
; 43(6): 486-495, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37253452
3.
V180I genetic Creutzfeldt-Jakob disease: Severe degeneration of the inferior olivary nucleus in an autopsied patient with identification of the M2T prion strain.
Neuropathology
; 43(6): 479-485, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37165430
4.
Methionine homozygosity for PRNP polymorphism and susceptibility to human prion diseases.
J Neurol Neurosurg Psychiatry
; 93(7): 779-784, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35387866
5.
An autopsy case of MV2K-type sporadic Creutzfeldt-Jakob disease presenting with characteristic clinical, radiological, and neuropathological findings.
Neuropathology
; 42(3): 245-253, 2022 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-35441383
6.
α2,3 linkage of sialic acid to a GPI anchor and an unpredicted GPI attachment site in human prion protein.
J Biol Chem
; 295(22): 7789-7798, 2020 05 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-32321762
7.
Potential for transmission of sporadic Creutzfeldt-Jakob disease through peripheral routes.
Lab Invest
; 101(10): 1327-1330, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34253850
8.
Detection of cutaneous prion protein deposits could help diagnose GPI-anchorless prion disease with neuropathy.
Eur J Neurol
; 28(6): 2133-2137, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33420752
9.
Genetic Creutzfeldt-Jakob disease-M232R with the cooccurrence of multiple prion strains, M1 + M2C + M2T: Report of an autopsy case.
Neuropathology
; 41(3): 206-213, 2021 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-33586250
10.
Characterization of Sporadic Creutzfeldt-Jakob Disease and History of Neurosurgery to Identify Potential Iatrogenic Cases.
Emerg Infect Dis
; 26(6): 1140-1146, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32442393
11.
Eliminating transmissibility of bovine spongiform encephalopathy by dry-heat treatment.
J Gen Virol
; 101(1): 136-142, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31718739
12.
Ganglioside Synthase Knockout Reduces Prion Disease Incubation Time in Mouse Models.
Am J Pathol
; 189(3): 677-686, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30553837
13.
A Novel Combination of Prion Strain Co-Occurrence in Patients with Sporadic Creutzfeldt-Jakob Disease.
Am J Pathol
; 189(6): 1276-1283, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30926338
14.
Identification of intracerebral hemorrhage in the early-phase of MM1+2C-type sporadic Creutzfeldt-Jakob disease: A case report.
Neuropathology
; 40(4): 399-406, 2020 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-32367540
15.
Transmission experiments verify sporadic V2 prion in a patient with E200K mutation.
Acta Neuropathol
; 147(1): 89, 2024 May 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-38767731
16.
Autopsied case of sporadic Creutzfeldt-Jakob disease classified as MM1+2C-type.
Neuropathology
; 39(3): 240-247, 2019 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-31062411
17.
Autopsy case of MV2K-type sporadic Creutzfeldt-Jakob disease with spongiform changes of the cerebral cortex.
Neuropathology
; 39(6): 452-460, 2019 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-31515858
18.
Biochemical features of genetic Creutzfeldt-Jakob disease with valine-to-isoleucine substitution at codon 180 on the prion protein gene.
Biochem Biophys Res Commun
; 496(4): 1055-1061, 2018 02 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-29382530
19.
Creutzfeldt-Jakob disease with Alzheimer pathology, presenting with status epilepticus following repeated partial seizures: a case report and literature review.
BMC Neurol
; 18(1): 54, 2018 Apr 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-29699515
20.
Autopsy case of V180I genetic Creutzfeldt-Jakob disease presenting with early disease pathology.
Neuropathology
; 38(6): 638-645, 2018 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-30216556