The online latin american registry of primary immunodeficiencies (2009)
- Autor:
- Autor USP: CONDINO NETO, ANTONIO - ICB
- Unidade: ICB
- Assunto: IMUNOLOGIA
- Language: Inglês
- Imprenta:
- Publisher place: San Francisco
- Date published: 2009
- Source:
- Título: Clinical Immunology
- Volume/Número/Paginação/Ano: v. 131, suppl. 1, 2009
- Conference titles: Annual Meeting of Federation of Clinical Immunology Societies - FOCIS
-
ABNT
CONDINO NETO, Antonio. The online latin american registry of primary immunodeficiencies. Clinical Immunology. San Francisco: Instituto de Ciências Biomédicas, Universidade de São Paulo. . Acesso em: 27 dez. 2025. , 2009 -
APA
Condino Neto, A. (2009). The online latin american registry of primary immunodeficiencies. Clinical Immunology. San Francisco: Instituto de Ciências Biomédicas, Universidade de São Paulo. -
NLM
Condino Neto A. The online latin american registry of primary immunodeficiencies. Clinical Immunology. 2009 ; 131[citado 2025 dez. 27 ] -
Vancouver
Condino Neto A. The online latin american registry of primary immunodeficiencies. Clinical Immunology. 2009 ; 131[citado 2025 dez. 27 ] - 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
- 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
- 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
- Molecular genetic analysis of Brazilian patients with CD40L deficiency
- IL-12/23-IFN-GAMMA axis defects and their effects on human NADPH oxidase system activation -myelomonocytic cell model
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