Amel Tej

Sousse, Tunisia

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 13 publications

Orbital Complications and Prognosis of Acute Ethmoiditis: A Pediatric Retrospective Observational Study.

Orbital Complications and Prognosis of Acute Ethmoiditis: A Pediatric Retrospective Observational Study.

Journal: Ear, nose, & throat journal

Published: May 19, 2026

Case Report: Compound heterozygous ITGB2 variants causing leukocyte adhesion deficiency type I With preserved CD18 expression.

Case Report: Compound heterozygous ITGB2 variants causing leukocyte adhesion deficiency type I With preserved CD18 expression.

Journal: Frontiers in immunology

Published: April 21, 2026

Comprehensive analysis of copy number variations in congenital heart defects Tunisian patients: chromosomal microarray analysis insights.

Comprehensive analysis of copy number variations in congenital heart defects Tunisian patients: chromosomal microarray analysis insights.

Journal: Molecular cytogenetics

Published: December 01, 2025

Prevalence of reported harassment and associated mental health outcomes among medical students: a cross-sectional study in Sousse, Tunisia.

Prevalence of reported harassment and associated mental health outcomes among medical students: a cross-sectional study in Sousse, Tunisia.

Journal: Scientific reports

Published: July 12, 2025

Recurrent pneumococcal meningitis in children: Diagnostic dilemma.

Recurrent pneumococcal meningitis in children: Diagnostic dilemma.

Journal: La Tunisie medicale

Published: April 29, 2024

Mitochondrial genes modulate the phenotypic expression of congenital scoliosis syndrome caused by mutations in the TBXT gene.

Mitochondrial genes modulate the phenotypic expression of congenital scoliosis syndrome caused by mutations in the TBXT gene.

Journal: Gene

Published: January 28, 2024

Disseminated BCG infection revealing a severe combined immunodeficiency: A case report.

Disseminated BCG infection revealing a severe combined immunodeficiency: A case report.

Journal: La Tunisie medicale

Published: January 01, 2022

Additional Tunisian patients with Sanjad-Sakati syndrome: A review toward a consensus on diagnostic criteria.

Additional Tunisian patients with Sanjad-Sakati syndrome: A review toward a consensus on diagnostic criteria.

Journal: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie

Published: July 22, 2018

Malignant hyperthermia in a 4-year-old girl during anesthesia induction with sevoflurane and succinylcholine for congenital ptosis surgery.

Malignant hyperthermia in a 4-year-old girl during anesthesia induction with sevoflurane and succinylcholine for congenital ptosis surgery.

Journal: Saudi journal of ophthalmology : official journal of the Saudi Ophthalmological Society

Published: March 02, 2018

Acute appendicitis complicating pregnancy: a 33 case series, diagnosis and management, features, maternal and neonatal outcomes.

Acute appendicitis complicating pregnancy: a 33 case series, diagnosis and management, features, maternal and neonatal outcomes.

Journal: The Pan African medical journal

Published: December 01, 2017

Clinical, Molecular, and Computational Analysis in two cases with mitochondrial encephalomyopathy associated with SUCLG1 mutation in a consanguineous family.

Clinical, Molecular, and Computational Analysis in two cases with mitochondrial encephalomyopathy associated with SUCLG1 mutation in a consanguineous family.

Journal: Biochemical and biophysical research communications

Published: November 21, 2017

Whole mitochondrial genome analysis in two families with dilated mitochondrial cardiomyopathy: detection of mutations in MT-ND2 and MT-TL1 genes.

Whole mitochondrial genome analysis in two families with dilated mitochondrial cardiomyopathy: detection of mutations in MT-ND2 and MT-TL1 genes.

Journal: Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis

Published: August 11, 2015

Showing 1-12 of 13

Last Updated: 09/26/2026