Complement 4 phenotypes and genotypes in Brazilian patients with classical 21-hydroxylase deficiency (2009)
- Authors:
- Guerra-Júnior, G. - Universidade Estadual de Campinas (UNICAMP)
- Grumach, Anete Sevciovic
- Lemos-Marini, S. H. Valente de - Universidade Estadual de Campinas (UNICAMP)
- Kirschfink, M.
- Condino Neto, Antônio
- Araújo, M. de - Universidade Estadual de Campinas (UNICAMP)
- De Mello, M. Palandi - Universidade Estadual de Campinas (UNICAMP)
- Autor USP: CONDINO NETO, ANTONIO - ICB
- Unidade: ICB
- DOI: 10.1111/j.1365-2249.2008.03838.x
- Assunto: IMUNOLOGIA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Clinical and Experimental Immunology
- ISSN: 0009-9104
- Volume/Número/Paginação/Ano: v. 155, n. 2, p. 182-188, 2009
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: bronze
-
ABNT
GUERRA-JÚNIOR, G. et al. Complement 4 phenotypes and genotypes in Brazilian patients with classical 21-hydroxylase deficiency. Clinical and Experimental Immunology, v. 155, n. 2, p. 182-188, 2009Tradução . . Disponível em: https://doi.org/10.1111/j.1365-2249.2008.03838.x. Acesso em: 17 abr. 2024. -
APA
Guerra-Júnior, G., Grumach, A. S., Lemos-Marini, S. H. V. de, Kirschfink, M., Condino Neto, A., Araújo, M. de, & De Mello, M. P. (2009). Complement 4 phenotypes and genotypes in Brazilian patients with classical 21-hydroxylase deficiency. Clinical and Experimental Immunology, 155( 2), 182-188. doi:10.1111/j.1365-2249.2008.03838.x -
NLM
Guerra-Júnior G, Grumach AS, Lemos-Marini SHV de, Kirschfink M, Condino Neto A, Araújo M de, De Mello MP. Complement 4 phenotypes and genotypes in Brazilian patients with classical 21-hydroxylase deficiency [Internet]. Clinical and Experimental Immunology. 2009 ; 155( 2): 182-188.[citado 2024 abr. 17 ] Available from: https://doi.org/10.1111/j.1365-2249.2008.03838.x -
Vancouver
Guerra-Júnior G, Grumach AS, Lemos-Marini SHV de, Kirschfink M, Condino Neto A, Araújo M de, De Mello MP. Complement 4 phenotypes and genotypes in Brazilian patients with classical 21-hydroxylase deficiency [Internet]. Clinical and Experimental Immunology. 2009 ; 155( 2): 182-188.[citado 2024 abr. 17 ] Available from: https://doi.org/10.1111/j.1365-2249.2008.03838.x - 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
Informações sobre o DOI: 10.1111/j.1365-2249.2008.03838.x (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
