Consensus statement for diagnosis of subcortical small vessel disease (2016)
- Authors:
- Autor USP: GRINBERG, LEA TENENHOLZ - FM
- Unidade: FM
- DOI: 10.1038/jcbfm.2015.172
- Subjects: INFLAMAÇÃO; DOENÇAS HEREDITÁRIAS; LÍQUIDO CEFALORRAQUIDIANO; IMAGEM POR RESSONÂNCIA MAGNÉTICA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Journal of Cerebral Blood Flow & Metabolism
- ISSN: 0271-678X
- Volume/Número/Paginação/Ano: v. 36, n. 1, p. 6-25, 2016
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: bronze
-
ABNT
ROSENBERG, Gary A. et al. Consensus statement for diagnosis of subcortical small vessel disease. Journal of Cerebral Blood Flow & Metabolism, v. 36, n. 1, p. 6-25, 2016Tradução . . Disponível em: https://doi.org/10.1038/jcbfm.2015.172. Acesso em: 23 abr. 2024. -
APA
Rosenberg, G. A., Wallin, A., Wardlaw, J. M., Markus, H. S., Montaner, J., Wolfson, L., et al. (2016). Consensus statement for diagnosis of subcortical small vessel disease. Journal of Cerebral Blood Flow & Metabolism, 36( 1), 6-25. doi:10.1038/jcbfm.2015.172 -
NLM
Rosenberg GA, Wallin A, Wardlaw JM, Markus HS, Montaner J, Wolfson L, Iadecola C, Zlokovic BV, Joutel A, Dichgans M, Duering M, Schmidt R, Korczyn AD, Grinberg LT, Chui HC, Hachinski V. Consensus statement for diagnosis of subcortical small vessel disease [Internet]. Journal of Cerebral Blood Flow & Metabolism. 2016 ; 36( 1): 6-25.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1038/jcbfm.2015.172 -
Vancouver
Rosenberg GA, Wallin A, Wardlaw JM, Markus HS, Montaner J, Wolfson L, Iadecola C, Zlokovic BV, Joutel A, Dichgans M, Duering M, Schmidt R, Korczyn AD, Grinberg LT, Chui HC, Hachinski V. Consensus statement for diagnosis of subcortical small vessel disease [Internet]. Journal of Cerebral Blood Flow & Metabolism. 2016 ; 36( 1): 6-25.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1038/jcbfm.2015.172 - Challenges in Modern Biomarker Discovery – 17th HUPO BPP Workshop
- Progranulin Mutations as Risk Factors for Alzheimer Disease
- Distinct tau prion strain propagate in cells and mice and define different tauopathies
- In vivo signatures of nonfluent/agrammatic primary progressive aphasia caused by FTLD pathology
- FTD phenotype in AD due to argyrophilic thorny astrocyte clusters
- Distinct tau prion strains propagate in cells and mice and define different tauopathies
- Primary age-related tauopathy (PART): a common pathology associated with human aging
- Genetic modifiers in carriers of repeat expansions in the C90RF72 gene
- The Latin American Brain Health Institute, a regional initiative to reduce the scale and impact of dementia
- Longitudinal multimodal imaging and clinical endpoints for frontotemporal dementia clinical trials
Informações sobre o DOI: 10.1038/jcbfm.2015.172 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas