Hypogammaglobulinemia and b cell lYmphopenia as phenotype associated with CD25 deficiency (2016)
- Authors:
- USP affiliated authors: SAMPAIO, MAGDA MARIA SALES CARNEIRO - FM ; KIM, CHONG AE - FM
- Unidade: FM
- DOI: 10.1007/s10875-016-0237-x
- Subjects: CRIANÇAS; AUTOIMUNIDADE; INFECÇÕES BACTERIANAS (ETIOLOGIA); DOENÇAS HEMATOLÓGICAS
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Journal of Clinical Immunology
- ISSN: 0271-9142
- Volume/Número/Paginação/Ano: v. 36, n. 3, p. 321, abstr. 4647, 2016
- Conference titles: Clinical Immunology Society - CIS Annual Meeting: Immune Deficiency & Dysregulation North American Conference
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: bronze
-
ABNT
SOARES, Diogo C. et al. Hypogammaglobulinemia and b cell lYmphopenia as phenotype associated with CD25 deficiency. Journal of Clinical Immunology. New York: Springer. Disponível em: https://doi.org/10.1007/s10875-016-0237-x. Acesso em: 19 set. 2024. , 2016 -
APA
Soares, D. C., Aquilante, B., Pastorino, A. C., Oliveira, J. B., Kim, C. A., & Carneiro-Sampaio, M. (2016). Hypogammaglobulinemia and b cell lYmphopenia as phenotype associated with CD25 deficiency. Journal of Clinical Immunology. New York: Springer. doi:10.1007/s10875-016-0237-x -
NLM
Soares DC, Aquilante B, Pastorino AC, Oliveira JB, Kim CA, Carneiro-Sampaio M. Hypogammaglobulinemia and b cell lYmphopenia as phenotype associated with CD25 deficiency [Internet]. Journal of Clinical Immunology. 2016 ; 36( 3): 321.[citado 2024 set. 19 ] Available from: https://doi.org/10.1007/s10875-016-0237-x -
Vancouver
Soares DC, Aquilante B, Pastorino AC, Oliveira JB, Kim CA, Carneiro-Sampaio M. Hypogammaglobulinemia and b cell lYmphopenia as phenotype associated with CD25 deficiency [Internet]. Journal of Clinical Immunology. 2016 ; 36( 3): 321.[citado 2024 set. 19 ] Available from: https://doi.org/10.1007/s10875-016-0237-x - Lymphoproliferative disorder with polyautoimmunity and hypogammaglobulinemia: An unusual presentation of 22q11.2 deletion syndrome
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Informações sobre o DOI: 10.1007/s10875-016-0237-x (Fonte: oaDOI API)
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