Genetic modifiers in carriers of repeat expansions in the C90RF72 gene (2014)
- Authors:
- Blitterswijk, Marka van
- Mullen, Bianca
- Wojtas, Aleksandra
- Heckman, Michael G.
- Diedhi, Nancy N.
- Baker, Matthew C.
- De Jesus-Hernandez, Mariely
- Brown, Patricia H.
- Murray, Melissa E.
- Hsiung, Ging-Yuek R.
- Stewart, Heather
- Karydas, Anna M.
- Finger, Elizabeth
- Kertesz, Andrew
- Bigio, Eileen H.
- Weintraub, Sandra
- Mesulam, Marsel
- Hatanpaa, Kimmo J.
- White III, Charles L.
- Neumann, Manuela
- Strong, Michael J.
- Beach, Thomas G.
- Wszolek, Zbigniew
- Lippa, Carol
- Caselli, Richard
- Petrucekki, Leonard
- Josephs, Keith
- Parisi, Joseph
- Knopman, David
- Peterson, Ronald
- Mackenzie, Ian
- Seeley, William
- Grinberg, Lea
- Miller, Bruce
- Boylan, Kevin
- Graff-Radford, Neil
- Boeve, Bradley
- Dickson, Dennis
- Rademakers, Rosa
- Autor USP: GRINBERG, LEA TENENHOLZ - FM
- Unidade: FM
- DOI: 10.1186/1750-1326-9-38
- Subjects: DOENÇAS NEURODEGENERATIVAS (DIAGNÓSTICO;TERAPIA); DEMÊNCIA (DIAGNÓSTICO;TERAPIA); MUTAÇÃO GENÉTICA; NEURÔNIOS (ANORMALIDADES)
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Molecular Neurodegeneration
- Volume/Número/Paginação/Ano: v. 9, p. 38, 2014
- Este periódico é de acesso aberto
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: gold
- Licença: cc-by
-
ABNT
BLITTERSWIJK, Marka van et al. Genetic modifiers in carriers of repeat expansions in the C90RF72 gene. Molecular Neurodegeneration, v. 9, p. 38, 2014Tradução . . Disponível em: https://doi.org/10.1186/1750-1326-9-38. Acesso em: 16 abr. 2024. -
APA
Blitterswijk, M. van, Mullen, B., Wojtas, A., Heckman, M. G., Diedhi, N. N., Baker, M. C., et al. (2014). Genetic modifiers in carriers of repeat expansions in the C90RF72 gene. Molecular Neurodegeneration, 9, 38. doi:10.1186/1750-1326-9-38 -
NLM
Blitterswijk M van, Mullen B, Wojtas A, Heckman MG, Diedhi NN, Baker MC, De Jesus-Hernandez M, Brown PH, Murray ME, Hsiung G-YR, Stewart H, Karydas AM, Finger E, Kertesz A, Bigio EH, Weintraub S, Mesulam M, Hatanpaa KJ, White III CL, Neumann M, Strong MJ, Beach TG, Wszolek Z, Lippa C, Caselli R, Petrucekki L, Josephs K, Parisi J, Knopman D, Peterson R, Mackenzie I, Seeley W, Grinberg L, Miller B, Boylan K, Graff-Radford N, Boeve B, Dickson D, Rademakers R. Genetic modifiers in carriers of repeat expansions in the C90RF72 gene [Internet]. Molecular Neurodegeneration. 2014 ; 9 38.[citado 2024 abr. 16 ] Available from: https://doi.org/10.1186/1750-1326-9-38 -
Vancouver
Blitterswijk M van, Mullen B, Wojtas A, Heckman MG, Diedhi NN, Baker MC, De Jesus-Hernandez M, Brown PH, Murray ME, Hsiung G-YR, Stewart H, Karydas AM, Finger E, Kertesz A, Bigio EH, Weintraub S, Mesulam M, Hatanpaa KJ, White III CL, Neumann M, Strong MJ, Beach TG, Wszolek Z, Lippa C, Caselli R, Petrucekki L, Josephs K, Parisi J, Knopman D, Peterson R, Mackenzie I, Seeley W, Grinberg L, Miller B, Boylan K, Graff-Radford N, Boeve B, Dickson D, Rademakers R. Genetic modifiers in carriers of repeat expansions in the C90RF72 gene [Internet]. Molecular Neurodegeneration. 2014 ; 9 38.[citado 2024 abr. 16 ] Available from: https://doi.org/10.1186/1750-1326-9-38 - 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
- 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
- Alzheimer's disease clinical variants show distinct regional patterns of neurofibrillary tangle accumulation
Informações sobre o DOI: 10.1186/1750-1326-9-38 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
