A simple method to distinguish between primary and second C3 deficiencies (2003)
- Authors:
- Autor USP: ISAAC, LOURDES - ICB
- Unidade: ICB
- Assunto: IMUNOLOGIA
- Language: Inglês
- Source:
- Título do periódico: Clinical Diagnostic Laboratory Immunology
- Volume/Número/Paginação/Ano: v. 10, p.216-220, 2003
-
ABNT
FLORIDO, M C P. e PAULA, P F. e ISAAC, Lourdes. A simple method to distinguish between primary and second C3 deficiencies. Clinical Diagnostic Laboratory Immunology, v. 10, p. 216-220, 2003Tradução . . Acesso em: 19 abr. 2024. -
APA
Florido, M. C. P., Paula, P. F., & Isaac, L. (2003). A simple method to distinguish between primary and second C3 deficiencies. Clinical Diagnostic Laboratory Immunology, 10, 216-220. -
NLM
Florido MCP, Paula PF, Isaac L. A simple method to distinguish between primary and second C3 deficiencies. Clinical Diagnostic Laboratory Immunology. 2003 ; 10 216-220.[citado 2024 abr. 19 ] -
Vancouver
Florido MCP, Paula PF, Isaac L. A simple method to distinguish between primary and second C3 deficiencies. Clinical Diagnostic Laboratory Immunology. 2003 ; 10 216-220.[citado 2024 abr. 19 ] - Ultrastructural aspects of alpha - 2 - macroglobulin activited mouse macrophages
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- Parcial analysis of factor I gene in two deficient sisters of this protein
- Um novo caso de deficiência de C3 do sistema complemento humano
- Immunological characterization of a human C3 deficiency
- Inherited complete factor I deficiency associated with systemic lupus enythematosus, higher susceptibility to infection and low levels of factor H
- Concentrations of regulatory complement proteins in Brazilian Nealthy children and adults
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