Mortality rate and causes of death in inborn errors of immunity: a systematic review and meta-analysis (2025)
- Authors:
- Fekrvand, Saba
- Esfahani, Zahra Hamidi
- Yarahmadi, Mohammadmehdi
- Boroujeni, Ali Saeedi
- Salehi, Helia
- Hakimelahi, Ali
- Hasiani, Amir Almasi
- Rahmati, Mahshid
- Ghasemlou, Sanaz Afshar
- Fard, Najmeh Nameh Goshay
- Monfared, Fateme Tarighat
- Afkham, Ehsan Khoshnezhad
- Fathi, Nazanin
- Shad, Tannaz Moeini
- Babaha, Fateme
- Nazari, Farzad
- Nirouei, Matineh
- Farid, Amir Salehi
- Sanadgol, Negin
- Rafiemanesh, Hosein
- Marzbali, Mahsa Yousefpour
- Hassanpour, Gholamreza
- Olbrich, Peter
- Condino Neto, Antonio
- Morio, Tomohiro
- Gennery, Andrew R.
- Meyts, Isabelle
- Ochs, Hans Dieter
- Abolhassani, Hassan
- Rezaei, Nima
- Yazdani, Reza
- Fekrvand, Saba
- Autor USP: CONDINO NETO, ANTONIO - ICB
- Unidade: ICB
- DOI: 10.1016/j.mrrev.2025.108564
- Subjects: IMUNOLOGIA; IMUNIDADE; IMUNODEFICIÊNCIA DE VARIÁVEL COMUM; MORTALIDADE; REVISÃO SISTEMÁTICA
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Source:
- Título: Mutation Research - Reviews in Mutation Research
- ISSN: 1388-2139
- Volume/Número/Paginação/Ano: v. 796, art. 108564, 15 p., 2025
- Este artigo NÃO possui versão em acesso aberto
-
Status: Nenhuma versão em acesso aberto identificada -
ABNT
FEKRVAND, Saba et al. Mortality rate and causes of death in inborn errors of immunity: a systematic review and meta-analysis. Mutation Research - Reviews in Mutation Research, v. 796, p. 15 , 2025Tradução . . Disponível em: https://doi.org/10.1016/j.mrrev.2025.108564. Acesso em: 12 mar. 2026. -
APA
Fekrvand, S., Esfahani, Z. H., Yarahmadi, M., Boroujeni, A. S., Salehi, H., Hakimelahi, A., et al. (2025). Mortality rate and causes of death in inborn errors of immunity: a systematic review and meta-analysis. Mutation Research - Reviews in Mutation Research, 796, 15 . doi:10.1016/j.mrrev.2025.108564 -
NLM
Fekrvand S, Esfahani ZH, Yarahmadi M, Boroujeni AS, Salehi H, Hakimelahi A, Hasiani AA, Rahmati M, Ghasemlou SA, Fard NNG, Monfared FT, Afkham EK, Fathi N, Shad TM, Babaha F, Nazari F, Nirouei M, Farid AS, Sanadgol N, Rafiemanesh H, Marzbali MY, Hassanpour G, Olbrich P, Condino Neto A, Morio T, Gennery AR, Meyts I, Ochs HD, Abolhassani H, Rezaei N, Yazdani R. Mortality rate and causes of death in inborn errors of immunity: a systematic review and meta-analysis [Internet]. Mutation Research - Reviews in Mutation Research. 2025 ; 796 15 .[citado 2026 mar. 12 ] Available from: https://doi.org/10.1016/j.mrrev.2025.108564 -
Vancouver
Fekrvand S, Esfahani ZH, Yarahmadi M, Boroujeni AS, Salehi H, Hakimelahi A, Hasiani AA, Rahmati M, Ghasemlou SA, Fard NNG, Monfared FT, Afkham EK, Fathi N, Shad TM, Babaha F, Nazari F, Nirouei M, Farid AS, Sanadgol N, Rafiemanesh H, Marzbali MY, Hassanpour G, Olbrich P, Condino Neto A, Morio T, Gennery AR, Meyts I, Ochs HD, Abolhassani H, Rezaei N, Yazdani R. Mortality rate and causes of death in inborn errors of immunity: a systematic review and meta-analysis [Internet]. Mutation Research - Reviews in Mutation Research. 2025 ; 796 15 .[citado 2026 mar. 12 ] Available from: https://doi.org/10.1016/j.mrrev.2025.108564 - 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
