Molecular-genetic defects in AICDA gene confirms clinical spectrum of autosomal hyper igm syndrome in brazilian patients (2012)
- Authors:
- Autor USP: CONDINO NETO, ANTONIO - ICB
- Unidade: ICB
- Assunto: IMUNOLOGIA
- Language: Inglês
- Imprenta:
- Publisher: The European Society for Immunodeficiencies
- Publisher place: Florença
- Date published: 2012
- Source:
- Título do periódico: Resumos
- Conference titles: Biennial Meenting of the European Society for Immunodeficiencies (ESID)
-
ABNT
KLAVER, S. et al. Molecular-genetic defects in AICDA gene confirms clinical spectrum of autosomal hyper igm syndrome in brazilian patients. 2012, Anais.. Florença: The European Society for Immunodeficiencies, 2012. . Acesso em: 24 abr. 2024. -
APA
Klaver, S., Carvalho, B., Tavares, F., Lima, S., Ferreira, J., Mansur, E., et al. (2012). Molecular-genetic defects in AICDA gene confirms clinical spectrum of autosomal hyper igm syndrome in brazilian patients. In Resumos. Florença: The European Society for Immunodeficiencies. -
NLM
Klaver S, Carvalho B, Tavares F, Lima S, Ferreira J, Mansur E, Roxo-Junior P, Durandy A, Condino-Neto A. Molecular-genetic defects in AICDA gene confirms clinical spectrum of autosomal hyper igm syndrome in brazilian patients. Resumos. 2012 ;[citado 2024 abr. 24 ] -
Vancouver
Klaver S, Carvalho B, Tavares F, Lima S, Ferreira J, Mansur E, Roxo-Junior P, Durandy A, Condino-Neto A. Molecular-genetic defects in AICDA gene confirms clinical spectrum of autosomal hyper igm syndrome in brazilian patients. Resumos. 2012 ;[citado 2024 abr. 24 ] - Anhidrotic ectodermal dysplasia and T cell immunodeficiency
- BAY 41-2272 aumenta a atividade microbicida in vitro de leucócitos mononucleares humanos
- The role of nuclear factor kappa B (NF-kB) on the NCF1 gene expression
- Essential role of nuclear factor-kappa B for NADPH oxidase activity in normal and anhidrotic ectodermal dysplasia leukocytes
- A single nucleotide polymorphism in the promoter region of the NCF-2 gene
- Essential role of nuclear factor-kappa B for NADPH oxidase activity, CYBB and NCF-1 gene expression in normal and anhidrotic ectodermal dysplasia leukocytes
- An unusual case of a female patient presenting with recurrent infections due to mycobacteria, viruses, and pyogenic bacteria and defective TLRs response
- Critical issues and needs in management of primary immunodeficiency diseases in Latin America
- Brain abscess as first clinical manifestation of hypogammaglobulinemia
- Essential role of Nuclear Factor kappa B (NF-jB) on NCFL gene expression in normal, anhidrotic ectodermal dysplasia, and chronic granulomatous disease leukocytes
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
