» Authors » Jalila El Bakkouri

Jalila El Bakkouri

Explore the profile of Jalila El Bakkouri including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 25
Citations 461
Followers 0
Related Specialties
Top 10 Co-Authors
Published In
Affiliations
Soon will be listed here.
Recent Articles
1.
El Azhary K, Ghazi B, Kouhen F, El Bakkouri J, Chamlal H, El Ghanmi A, et al.
Diagnostics (Basel) . 2025 Feb; 15(4). PMID: 40002608
: Corona virus disease 2019 (COVID-19) poses a threat to global public health. The early identification of critical cases is crucial to providing timely treatment to patients. Here, we investigated...
2.
Chihi M, Barakat L, Benhayoun F, Allaoui A, Housbane S, Moudatir M, et al.
Clin Pract . 2025 Feb; 15(2). PMID: 39996701
Dermatomyositis (DM) is a rare idiopathic inflammatory myopathy characterized by muscle weakness and typical cutaneous rash. Dermatomyositis-specific antibodies, such as anti-TIF1γ, anti-SAE, anti-Mi2, anti-MDA5, and anti-NXP2, have been associated with...
3.
Moundir A, Aissaoui O, Akhrichi N, Allaoui A, Benhsaien I, Jouanguy E, et al.
Clin Exp Immunol . 2025 Feb; PMID: 39918293
Introduction: Increasing evidence supports the involvement of inborn errors of immunity (IEI) in severe infections, but little is known about the prevalence of these genetic defects in children with sepsis....
4.
Kasmi Z, Ain El Hayat I, Aadam Z, Errami A, Benhsaien I, El Bakkouri J, et al.
BMC Med Genomics . 2025 Feb; 18(1):25. PMID: 39901213
No abstract available.
5.
Aissaoui O, Moundir A, Drissi Boughanbour A, El Bakkouri J, Benhsaien I, Ailal F, et al.
Tunis Med . 2025 Jan; 103(1):93-97. PMID: 39812200
Introduction: Pediatric sepsis remains a leading cause of morbidity and mortality in Africa. Nearly half of pediatric sepsis deaths occur in previously healthy children. The role of inborn errors of...
6.
Kasmi Z, Chihi M, Aadam Z, Ouair H, Drissi Bourhanbour A, El Bakkouri J, et al.
Immunol Res . 2025 Jan; 73(1):29. PMID: 39779505
Congenital neutropenia (CoN) is a heterogeneous group of inborn errors of immunity (IEI) characterized by recurrent infections and early onset of neutropenia (NP). This study aimed to investigate the demographic...
7.
Kasmi Z, Ain El Hayat I, Aadam Z, Errami A, Benhsaien I, El Bakkouri J, et al.
BMC Med Genomics . 2025 Jan; 18(1):5. PMID: 39773724
Glycogen Storage Disease Type Ib (GSD-Ib) is a rare autosomal recessive metabolic disorder caused by mutations in SLC37A4, leading to a deficiency in glucose-6-phosphate translocase. This disorder is characterized by...
8.
Fadil I, Benhsaien I, El Bakkouri J, Jeddane L, Benaajiba N, Rada N, et al.
Tunis Med . 2024 Oct; 102(10):696-701. PMID: 39441153
Introduction: Hyper-IgE syndrome is a group of inborn errors of immunity, some of which are syndromic, characterized clinically by the classic triad of chronic eczema, cutaneous and/or pulmonary staphylococcal infections...
9.
El Kettani A, Ouair H, Marnissi F, El Bakkouri J, Chevalier R, Lorenzo L, et al.
Viruses . 2024 Sep; 16(9). PMID: 39339890
Epidermodysplasia verruciformis (EV) is a rare genodermatosis caused by β-human papillomaviruses (HPV) in immunodeficient patients. EV is characterized by flat warts and pityriasis-like lesions and might be isolated or syndromic,...
10.
Kholaiq H, Abdelmoumen Y, Moundir A, El Kettani A, Ailal F, Benhsaien I, et al.
Clin Exp Immunol . 2024 Jul; 219(1). PMID: 39028583
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) induces pneumonia and acute respiratory failure in coronavirus disease 2019 (COVID-19) patients with inborn errors of immunity to type I interferon (IFN-I). The...