AC
Amel Ben Chehida

Publications (7)

Case Report: Dual molecular diagnosis of gain-of-function STAT1 mutation and regulatory STAT3 variant in a patient with a hyper-IgE-like phenotype
Article scientifique · 2025
Case Report: Primary bile acid synthesis defect: first cases series from Tunisia
Article scientifique · 2026
Identification of mutations that causes glucose-6-phosphate transporter defect in tunisian patients with glycogenosis type 1b
Article scientifique · 2023
Identification of mutations that causes glucose-6-phosphate transporter defect in Tunisian patients with glycogenosis type 1b
Article scientifique · 2023
A severe clinical phenotype of Noonan syndrome with neonatal hypertrophic cardiomyopathy in the second case worldwide withRAF1S259Y neomutation
Article scientifique · 2019
Correction to: Full title: peripheral venous catheter complications in children: predisposing factors in a multicenter prospective cohort study
Article scientifique · 2018
Full title: peripheral venous catheter complications in children: predisposing factors in a multicenter prospective cohort study
Article scientifique · 2017

Domaines principaux

Sciences de la santé6 Sciences de la vie et biotechnologies1

Statistiques

Consultations20
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