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Amel Tej
Affiliation : University of Monastir · Hôpital Farhat Hached · University of Sousse
- 20Publications (affiliation in Tunisia)
- 32Total publications
- 74Citations
- 5h-index
Research profile
Amel Tej has 20 indexed publications (2014–2026). Their work appears mainly in “Scientific Reports”, “Ear Nose & Throat Journal” and “Research Square”. Their most cited article, “Acute appendicitis complicating pregnancy: a 33 case series, diagnosis and management features, maternal and neonatal outcomes” (2018), has been cited 25 times. 11 of these publications date from the last three years of activity. Their work is co-authored with at least 12 researchers.
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Create my free profile Add my publicationsResearch areas
- Genomics and Rare Diseases
- Immunodeficiency and Autoimmune Disorders
- Mitochondrial Function and Pathology
- Otolaryngology and Infectious Diseases
- Adrenal Hormones and Disorders
Publications (20)
- Prevalence of reported harassment and associated mental health outcomes among medical students: a cross-sectional study in Sousse, Tunisia
- Orbital Complications and Prognosis of Acute Ethmoiditis: A Pediatric Retrospective Observational Study
- Evaluation of HPA Axis Function in Pediatric Patients with Chronic Corticosteroid Therapy Using the Low-Dose (1 μg) Synacthen Test
- Comprehensive analysis of copy number variations in congenital heart defects Tunisian patients: chromosomal microarray analysis insights
- New Cortisol Thresholds for the Diagnosis of Adrenal Insufficiency Using the Low-Dose Synacthen Test in Children on Long-Term Corticosteroids: A North African Pilot Study
- Comparative phytochemical profiling, antioxidant activity, and subacute toxicity assessment of infusion and decoction extracts of pumpkin seeds
- Case Report: Compound heterozygous ITGB2 variants causing leukocyte adhesion deficiency type I With preserved CD18 expression
- Clinical and genomic characterization of corpus callosum abnormalities (CCA) in 107 Tunisian patients using a stepwise diagnostic approach
- Management of pediatric acute mastoiditis: A single-center experience over two decades
- Mitochondrial genes modulate the phenotypic expression of congenital scoliosis syndrome caused by mutations in the TBXT gene
- Recurrent pneumococcal meningitis in children: Diagnostic dilemma.
- Paediatric critical COVID-19: clinical features and outcomes during five waves.
- Paediatric critical COVID-19: clinical features and outcomes during five waves.
- Bilateral pheochromocytoma revealed by acute abdominal pain in a child. A case report
- Acute appendicitis complicating pregnancy: a 33 case series, diagnosis and management features, maternal and neonatal outcomes
- Malignant hyperthermia in a 4-year-old girl during anesthesia induction with sevoflurane and succinylcholine for congenital ptosis surgery
- Clinical, Molecular, and Computational Analysis in two cases with mitochondrial encephalomyopathy associated with SUCLG1 mutation in a consanguineous family
- Hypomagnesemia with Secondary Hypocalcemia Linked to a Novel TRPM6 Gene Mutation
- Whole mitochondrial genome analysis in two families with dilated mitochondrial cardiomyopathy: detection of mutations in MT-ND2 and MT-TL1 genes
- Chediak–Higashi Syndrome Presented as Accelerated Phase: Case Report and Review of the Literature
Publication venues
- Scientific Reports × 1
- Ear Nose & Throat Journal × 1
- Research Square × 1
- Molecular Cytogenetics × 1
- Diagnostics × 1
- INNOSC Theranostics and Pharmacological Sciences × 1
Publications per year
- 20268
- 20251
- 20242
- 20222
- 20201
- 20182
- 20171
- 20161
- 20151
- 20141
Collaborations
Partner institutions : University of Sfax · Hôpital Sahloul · Faculty of Medicine of Sfax · Faculty of Sciences of Sfax · University of Kairouan
Co-authors
- Lamia Boughamoura
- Jihène Bouguila
- Raoudha Kebaïli
- Samia Tilouche
- Najla Soyah
- Nesrine Jaballah
- Marwa Abdelbari
- Hajer Ben Belgacem
- Lamia Boughammoura
- Nejla Soyah
- Faiza Fakhfakh
- Amira Benzarti
Bibliographic data from OpenAlex (open database).
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