Analysis of the interleukin-1 gene complex in LOAD brazilian patients (2003)
- Authors:
- USP affiliated authors: ZATZ, MAYANA - IB ; NITRINI, RICARDO - FM
- Unidades: IB; FM
- Subjects: TRANSTORNOS MENTAIS; DOENÇAS GENÉTICAS
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: American Journal of Human Genetics
- Volume/Número/Paginação/Ano: v. 73, n. 5, supl., p. 468, 2003
- Conference titles: Annual Meeting of the American Society of Human Genetics
-
ABNT
NISHIMURA, Agnes L.; MURY, F. B.; MITNE-NETO, M.; et al. Analysis of the interleukin-1 gene complex in LOAD brazilian patients. American Journal of Human Genetics[S.l: s.n.], 2003. -
APA
Nishimura, A. L., Mury, F. B., Mitne-Neto, M., Oliveira, J. R. M., Nitrini, R., Bahia, V. S., et al. (2003). Analysis of the interleukin-1 gene complex in LOAD brazilian patients. American Journal of Human Genetics. Baltimore. -
NLM
Nishimura AL, Mury FB, Mitne-Neto M, Oliveira JRM, Nitrini R, Bahia VS, Brito-Marques PR, Neri M, Fertuzinhos SMM, Zatz M. Analysis of the interleukin-1 gene complex in LOAD brazilian patients. American Journal of Human Genetics. 2003 ; 73( 5): 468. -
Vancouver
Nishimura AL, Mury FB, Mitne-Neto M, Oliveira JRM, Nitrini R, Bahia VS, Brito-Marques PR, Neri M, Fertuzinhos SMM, Zatz M. Analysis of the interleukin-1 gene complex in LOAD brazilian patients. American Journal of Human Genetics. 2003 ; 73( 5): 468. - Analysis of the DXS1047 region in Brazil: ian patients with Alzheimer´s disease
- Análise do locus DXS1047 em pacientes brasileiros com doença de Alzheimer
- Associação entre o complexo gênico IL-1 e a doença de Alzheimer
- Another locus for autosomal dominant late onset Alzheimers disease in brazilian families?
- Association studies with MAOA and BDNF polymorphisms in brazilian patients affected by late onset Alzheimer disease
- Monoamine oxidase a polymorphism in brazilian patients
- Lack of association between the brain-derived neurotrophin factor (C-270T) polymorphism and late-onset Alzheimers disease (LOAD) in Brazilian patients
- Prion protein mutation with clinical features similar to frontotemporal dementia and parkinsonism kinked to chromossome 17 (FTDP-17)
- Association studies in Alzheimer's disease: perspective for new therapeutic approaches
- Estudos de associacao em doenca de Alzheimer: perspectivas para novos tratamentos
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