6 Apr 2026Open access
Levels of IL-1β and IL-1 receptor antagonist (IL-1Ra) in Moroccan children admitted to the pediatric emergency department for febrile seizuresPublisher siteBMC Pediatrics, Epilepsy research and treatment
UniversitiesAhmed Aziz Bousfiha
Active, last published 2026
Ahmed Aziz
Bousfiha
Scholar“Research profile drawn from open scholarly records.”
Centre Hospitalier Universitaire Ibn Rochd
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UPGRADE
01 · About the work
What I study
research summary for Ahmed Aziz Bousfiha will appear here once their profile is updated.
02 · Reach
Publication output and reach
Ahmed's work has been cited 101 times across 3 active years. Bars show publications per year; the line shows cumulative citation totals across publications first appearing in each year.
04 · Where I am
Affiliations
Affiliation on published researchCentre Hospitalier Universitaire Ibn RochdDrawn from the institution listed on this researcher’s published work.
Research themes (UN SDGs)
05 · Selected work
Recent publications
19 works18 Dec 2024Open access
Characterization of Aminoglycoside-Modifying Enzymes in Uropathogenic Enterobacterales of Community Origin in Casablanca, MoroccoPublisher siteActa Microbiologica Hellenica, Urinary Tract Infections Management
25 Nov 2024Open access1cites
Phenotype–genotype correlation in children with familial Mediterranean fever in MoroccoPublisher siteQatar medical journal, Inflammasome and immune disorders
13 Nov 2024Open access1cites
Innate immunodeficiencies: a group of primary immunodeficiencies predisposing exclusively to common diseasesPublisher siteEgyptian Journal of Medical Human Genetics, Immunodeficiency and Autoimmune Disorders
8 Oct 2024Open access1cites
Phenotypes of 126 Moroccan HIES patients according to NIH ScorePublisher siteLa Tunisie Médicale, Immunodeficiency and Autoimmune Disorders
10 Sept 202433cites
Complement system activation: bridging physiology, pathophysiology, and therapyPublisher siteIntensive Care Medicine, Complement system in diseases
5 Sept 2024Open access1cites
Case Report of Two Independent Moroccan Families with Syndromic Epidermodysplasia Verruciformis and STK4 DeficiencyPublisher siteViruses, Genetic and rare skin diseases.
28 Jul 2024Open access1cites
Prédisposition génétique à la Méningite Tuberculeuse : Compréhension des interactions cellulaires, mécanismes moléculaires et dimensions génétiques.Publisher siteLa Tunisie Médicale, Tuberculosis Research and Epidemiology
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