IgA deficiency in a patient with multiple hereditary exostoses (2008)
- Authors:
- Autor USP: SAMPAIO, MAGDA MARIA SALES CARNEIRO - FM
- Unidade: FM
- Subjects: IMUNOGLOBULINAS; DOENÇAS AUTOIMUNES; RESUMOS (EVENTOS)
- Language: Inglês
- Imprenta:
- Source:
- Título: Clinical and Experimental Immunology
- Volume/Número/Paginação/Ano: v. 154, suppl. 1, p. 176, res. A015, 2008
- Conference titles: Meeting of The European Society for Immunodeficiency
-
ABNT
KUNTZE, G. et al. IgA deficiency in a patient with multiple hereditary exostoses. Clinical and Experimental Immunology. London: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 09 jan. 2026. , 2008 -
APA
Kuntze, G., Sampaio, M. C., Melo, K., Dantas, E., Nudelman, V., Arslanian, C., et al. (2008). IgA deficiency in a patient with multiple hereditary exostoses. Clinical and Experimental Immunology. London: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Kuntze G, Sampaio MC, Melo K, Dantas E, Nudelman V, Arslanian C, Lawrence T, Costa Carvalho BT. IgA deficiency in a patient with multiple hereditary exostoses. Clinical and Experimental Immunology. 2008 ; 154 176.[citado 2026 jan. 09 ] -
Vancouver
Kuntze G, Sampaio MC, Melo K, Dantas E, Nudelman V, Arslanian C, Lawrence T, Costa Carvalho BT. IgA deficiency in a patient with multiple hereditary exostoses. Clinical and Experimental Immunology. 2008 ; 154 176.[citado 2026 jan. 09 ] - Antibody response to polysaccharide antigens in patients with Down syndrome
- Anti-C1q antibodies in patients with juvenile-onset systemic lupus erythematosus
- Antibody placental transfer and colostrum anti-infectious activity from mothers with common variable immunodeficiency receiving intravenous immunoglobulin
- Autoimmunity in Kabuki syndrome
- Early-onset autoimmune disease as a manifestation of primary immunodeficiency
- Autoimmune lymphoproliferative syndrome in a brazilian child
- Is hypergammaglobulinemia possible in SCID?
- É com grande satisfação que lançamos o ABC da saúde infantojuvenil por ocasião das comemorações dos 40 anos de atividades... [Apresentação]
- Primary immunodeficiencies (PIDs) are more frequently associated with juvenile systemic lupus erythematosus (JSLE) than antecipated
- IgA deficiency and multiplic hereditary exostose
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas