Correction to: Screening for antibody Deficiencies in adults by serum electrophoresis and calculated globulin (2023)
- Authors:
- Autor USP: CONDINO NETO, ANTONIO - ICB
- Unidade: ICB
- DOI: 10.1007/s10875-023-01536-1
- Subjects: IMUNOLOGIA; ANTICORPOS; ELETROFORESE; HEMOGLOBINAS; IMUNOGLOBULINAS
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Publisher: Springer New York LLC
- Publisher place: New York
- Date published: 2023
- Source:
- Título: Journal of Clinical Immunology
- ISSN: 0271-9142
- Volume/Número/Paginação/Ano: p. 1-8, 2023
- Status:
- Nenhuma versão em acesso aberto identificada
-
ABNT
PIZA, Cristina Frias Sartorelli de Toledo et al. Correction to: Screening for antibody Deficiencies in adults by serum electrophoresis and calculated globulin. Journal of Clinical Immunology, p. 1-8, 2023Tradução . . Disponível em: https://doi.org/10.1007/s10875-023-01536-1. Acesso em: 14 abr. 2026. -
APA
Piza, C. F. S. de T., Aranda, C. S., Sole, D., Jolles, S., & Condino Neto, A. (2023). Correction to: Screening for antibody Deficiencies in adults by serum electrophoresis and calculated globulin. Journal of Clinical Immunology, 1-8. doi:10.1007/s10875-023-01536-1 -
NLM
Piza CFS de T, Aranda CS, Sole D, Jolles S, Condino Neto A. Correction to: Screening for antibody Deficiencies in adults by serum electrophoresis and calculated globulin [Internet]. Journal of Clinical Immunology. 2023 ; 1-8.[citado 2026 abr. 14 ] Available from: https://doi.org/10.1007/s10875-023-01536-1 -
Vancouver
Piza CFS de T, Aranda CS, Sole D, Jolles S, Condino Neto A. Correction to: Screening for antibody Deficiencies in adults by serum electrophoresis and calculated globulin [Internet]. Journal of Clinical Immunology. 2023 ; 1-8.[citado 2026 abr. 14 ] Available from: https://doi.org/10.1007/s10875-023-01536-1 - Infecção por Blastomicose em pacientes com Hiper IgM ligada ao X (HIGM1)
- Papel essencial do nf-kappab na expressão dos genes ncf1 e ncf2 do sistema nadph oxidase em leucócitos saudáveis e de pacientes com displasia ectodérmica anidrótica (eda-id), doença granulomatosa crônica (cgd) ou com defeitos no eixo il-12/23-ifngamma.
- Humoral deficiency in a novel GATA2 mutation: anew clinical presentation successfully treated with hematopoietic stem cell transplantation
- IFN-β, IFN-γ, and TNF-α decrease erythrophagocytosis by human monocytes independent of SIRP-α or SHP-1 expression
- Do HLA class II genes protect against pulmonary tuberculosis? A systematic review and meta-analysis
- Toll-like receptors’ pathway disturbances are associated with increased susceptibility to infections in humans
- ICON: the early diagnosis of congenital immunodeficiencies
- Regulation of CYBB gene expression in human phagocytes by a distant upstream NF-κB binding site
- The first Iranian cohort of pediatric patients with activated phosphoinositide 3-kinase-δ (PI3Kδ) syndrome (APDS)
- Hematologically important mutations: X-linked chronic granulomatous disease (fourth update)
Informações sobre a disponibilidade de versões do artigo em acesso aberto coletadas automaticamente via oaDOI API (Unpaywall).
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
