日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Case Report: IL2RA (CD25) deficiency: first reported cases in Morocco

病例报告:IL2RA(CD25)缺乏症:摩洛哥首例报告病例

Elamine, Ahamada; Benhsaien, Ibtihal; Errami, Abderrahmane; Bellarhrib, Yousra; Aadam, Zahra; Fahi, Mohammed; Bousfiha, Ahmed Aziz; El Bakkouri, Jalila; Ailal, Fatima

Autoimmunity and inborn errors of immunity: a complex coexistence

自身免疫性疾病与先天性免疫缺陷:一种复杂的共存关系

Elamine, Ahamada; Benhsaien, Ibtihal; Ailal, Fatima; Hbibi, Mohammed; Fahi, Mohammed; Bousfiha, Ahmed Aziz; El Bakkouri, Jalila

Clinical, immunological, and genetic landscape of common variable immunodeficiency in Morocco: a nationwide multicenter study

摩洛哥常见变异型免疫缺陷的临床、免疫学和遗传学特征:一项全国多中心研究

Allaoui, Abire; Moundir, Abderrahmane; Benhsaien, Ibtihal; Ailal, Fatima; Bakkouri, Jalila El; Echchilali, Khadija; Naitlho, Abdelhamid; Kabli, Hassan El; Bousfiha, Ahmed Aziz; Moudatir, Mina

Case Report: A novel CIITA mutation causing MHC class II deficiency: first reported case in Morocco

病例报告:一种导致MHC II类缺陷的新型CIITA突变:摩洛哥首例报告病例

Kattra, Aziza Bachir; Ailal, Fatima; Benhsaien, Ibtihal; Fahi, Mohammed; Drissi Bourhanbour, Asmaa; Elamine, Ahamada; Aadam, Zahra; Errami, Abderrahmane; Bousfiha, Ahmed Aziz; El Bakkouri, Jalila

Human genetic and immunological determinants of SARS-CoV-2 infection and multisystem inflammatory syndrome in children

儿童SARS-CoV-2感染和多系统炎症综合征的人类遗传和免疫学决定因素

Kholaiq, Halima; Abdelmoumen, Yousra; Moundir, Abderrahmane; El Kettani, Assiya; Ailal, Fatima; Benhsaien, Ibtihal; Adnane, Fatima; Drissi Bourhanbour, Asmaa; Amenzoui, Naima; El Bakkouri, Jalila; Bousfiha, Ahmed Aziz

Application of whole-exome sequencing to predict inborn errors of immunity in pediatric severe infections and sepsis

应用全外显子组测序预测儿童重症感染和脓毒症中的先天性免疫缺陷

Moundir, Abderrahmane; Aissaoui, Ouissal; Akhrichi, Nassima; Allaoui, Abire; Benhsaien, Ibtihal; Jouanguy, Emmanuelle; Casanova, Jean-Laurent; El Bakkouri, Jalila; Ailal, Fatima; Bousfiha, Ahmed Aziz

Autoimmune manifestations in children with inborn errors of immunity in Morocco: A study from the national registry

摩洛哥先天性免疫缺陷患儿的自身免疫表现:一项基于国家登记处的研究

Elamine, Ahamada; Benhsaien, Ibtihal; Ailal, Fatima; Errami, Abderrahmane; Kasmi, Zakaria; Aadam, Zahra; Bourhanbour, Asmaa Drissi; Bousfiha, Ahmed Aziz; El Bakkouri, Jalila

Hypercalcemia and co-occurring TBX1 mutation in Glycogen Storage Disease Type Ib: case report

糖原贮积症Ib型合并高钙血症及TBX1基因突变:病例报告

Kasmi, Zakaria; Ain El Hayat, Imane; Aadam, Zahra; Errami, Abderrahmane; Benhsaien, Ibtihal; El Bakkouri, Jalila; Ben Sabbahia, Dalal; Atrassi, Meryem; Bousfiha, Ahmed Aziz; Ailal, Fatima

Correction: Hypercalcemia and co-occurring TBX1 mutation in Glycogen Storage Disease Type Ib: case report

更正:Ib型糖原贮积症合并高钙血症和TBX1基因突变:病例报告

Kasmi, Zakaria; Ain El Hayat, Imane; Aadam, Zahra; Errami, Abderrahmane; Benhsaien, Ibtihal; El Bakkouri, Jalila; Ben Sabbahia, Dalal; Atrassi, Meryem; Bousfiha, Ahmed Aziz; Ailal, Fatima

Major Histocompatibility Complex Class II Deficiency Beyond Infancy

婴儿期后主要组织相容性复合体 II 类缺乏症

Kattra, Aziza Bachir; Benhsaien, Ibtihal; Drissi Bourhanbour, Asmaa; Aadam, Zahra; Errami, Abderrahmane; Ailal, Fatima; Bousfiha, Ahmed Aziz; El Bakkouri, Jalila