Concomitant factor I and IgA deficiencies in a brazilian child (1998)
- Authors:
- Autor USP: ISAAC, LOURDES - ICB
- Unidade: ICB
- Assunto: IMUNOLOGIA
- Language: Inglês
- Imprenta:
- Source:
- Título: Molecular Immunology
- Volume/Número/Paginação/Ano: v. 35, n. 6-7, p. 358-res.112, 1998
- Conference titles: International Complement Workshop of Molecular Immunology
-
ABNT
AMADEI, N et al. Concomitant factor I and IgA deficiencies in a brazilian child. Molecular Immunology. Oxford: Instituto de Ciências Biomédicas, Universidade de São Paulo. . Acesso em: 09 jan. 2026. , 1998 -
APA
Amadei, N., Ferreira de Paula, P., Florido, M. P. C., Bastos, W., Nudelman, V., & Isaac, L. (1998). Concomitant factor I and IgA deficiencies in a brazilian child. Molecular Immunology. Oxford: Instituto de Ciências Biomédicas, Universidade de São Paulo. -
NLM
Amadei N, Ferreira de Paula P, Florido MPC, Bastos W, Nudelman V, Isaac L. Concomitant factor I and IgA deficiencies in a brazilian child. Molecular Immunology. 1998 ; 35( 6-7): 358-res.112.[citado 2026 jan. 09 ] -
Vancouver
Amadei N, Ferreira de Paula P, Florido MPC, Bastos W, Nudelman V, Isaac L. Concomitant factor I and IgA deficiencies in a brazilian child. Molecular Immunology. 1998 ; 35( 6-7): 358-res.112.[citado 2026 jan. 09 ] - Ligação de leptospira interrogans serovar pomona às diferentes variantes de fator H (TYR402 and HIS402)
- Intravitreal levels of human complement factor F (CFH) in patients with exudative age-related macular degeneration (AMD)
- Associação entre polimorfismo de fator H (Y402H) e degeneração da mácula relacionada à idade
- Association of the Y402H polymorphism in complement factor h gene and age-related macular degeneration in brazilians
- ARG 127 his substitution in SCR-2 of the regulatory complement protein factor H is found in a factor H deficient patient with concomitant lack of complement component C9
- Characterization and genetic analysis of human complement Factor I deficiency
- Immunological and genetic characterization of deficiency of the component C5 of the human complement system
- Human complement factor H (Y402H) polymorphism and age-related macular degeneration (AMD) in brazilian patients
- A missense mutation is associated with the regulatory complement protein factor H deficiency in a patient with concomitant lack of complement component C9
- Leptospira Immunoglobulin-like proteins bind human complement regulator Factor H
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