A rare form of sporadic Jakob-Creutzfeldt disease presenting as PSP: A Public Health Issue (2015)
- Authors:
- Autor USP: GRINBERG, LEA TENENHOLZ - FM
- Unidade: FM
- Subjects: DEMÊNCIA; TRANSTORNOS DA MOTILIDADE OCULAR; DOENÇAS CEREBRAIS
- Language: Inglês
- Imprenta:
- Source:
- Título: Journal of Neuropathology and Experimental Neurology
- ISSN: 0022-3069
- Volume/Número/Paginação/Ano: v. 74, n. 6, p. 601, abst. 49, 2015
- Conference titles: Annual Meeting of the American Association of Neuropathologists
-
ABNT
GRINBERG, Lea et al. A rare form of sporadic Jakob-Creutzfeldt disease presenting as PSP: A Public Health Issue. Journal of Neuropathology and Experimental Neurology. Baltimore: Faculdade de Medicina, Universidade de São Paulo. Disponível em: file:///C:/Users/DBDFMUSP/Downloads/American_Association_of_Neuropathologists,_Inc_.12.pdf. Acesso em: 22 jan. 2026. , 2015 -
APA
Grinberg, L., Fernandez-Fournier, M., Perry, D., Tartaglia, M., DeMay, M., Boxer, A., et al. (2015). A rare form of sporadic Jakob-Creutzfeldt disease presenting as PSP: A Public Health Issue. Journal of Neuropathology and Experimental Neurology. Baltimore: Faculdade de Medicina, Universidade de São Paulo. Recuperado de file:///C:/Users/DBDFMUSP/Downloads/American_Association_of_Neuropathologists,_Inc_.12.pdf -
NLM
Grinberg L, Fernandez-Fournier M, Perry D, Tartaglia M, DeMay M, Boxer A, Coppola G, Christine C, Gambetti P, Cali I, Seeley W, Miller B, deArmond S, Geschwind M. A rare form of sporadic Jakob-Creutzfeldt disease presenting as PSP: A Public Health Issue [Internet]. Journal of Neuropathology and Experimental Neurology. 2015 ; 74( 6): 601.[citado 2026 jan. 22 ] Available from: file:///C:/Users/DBDFMUSP/Downloads/American_Association_of_Neuropathologists,_Inc_.12.pdf -
Vancouver
Grinberg L, Fernandez-Fournier M, Perry D, Tartaglia M, DeMay M, Boxer A, Coppola G, Christine C, Gambetti P, Cali I, Seeley W, Miller B, deArmond S, Geschwind M. A rare form of sporadic Jakob-Creutzfeldt disease presenting as PSP: A Public Health Issue [Internet]. Journal of Neuropathology and Experimental Neurology. 2015 ; 74( 6): 601.[citado 2026 jan. 22 ] Available from: file:///C:/Users/DBDFMUSP/Downloads/American_Association_of_Neuropathologists,_Inc_.12.pdf - The Latin American Brain Health Institute, a regional initiative to reduce the scale and impact of dementia
- Light at the beginning of the tunnel?: investigating early mechanistic changes in Alzheimer’s disease
- Argyrophilic grain disease differs from other tauopathies by lacking tau acetylation
- On the origin of tau seeding activity in Alzheimer's disease
- New milestones in the development of characterization tools for neurodegenerative diseases in proteomics
- Key players in neurodegenerative disorders in focus—New insights into the proteomic profile of Alzheimer's disease, schizophrenia, ALS, and multiple sclerosis—24th HUPO BPP Workshop
- In vivo signatures of nonfluent/agrammatic primary progressive aphasia caused by FTLD pathology
- Distinct tau prion strain propagate in cells and mice and define different tauopathies
- Sleepless Night and Day, the Plight of Progressive Supranuclear Palsy
- Alzheimer's disease clinical variants show distinct regional patterns of neurofibrillary tangle accumulation
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas