Amel Tej

الانتماء : University of Monastir · Hôpital Farhat Hached · University of Sousse

20منشورات (انتماء تونسي)
32مجموع المنشورات
74الاستشهادات
5مؤشر h

الملف البحثي

لدى Amel Tej 20 منشور(ات) مفهرسة (2014–2026). تُنشر أعماله أساسًا في «Scientific Reports»، «Ear Nose & Throat Journal» و«Research Square». أكثر مقالاته استشهادًا هو «Acute appendicitis complicating pregnancy: a 33 case series, diagnosis and management features, maternal and neonatal outcomes» (2018)، وقد استُشهد به 25 مرة. 11 من هذه المنشورات تعود إلى آخر ثلاث سنوات من النشاط. شارك في تأليف أعماله 12 باحثًا على الأقل.

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إنشاء ملفي المجاني إضافة منشوراتي

مجالات البحث

Genomics and Rare Diseases
Immunodeficiency and Autoimmune Disorders
Mitochondrial Function and Pathology
Otolaryngology and Infectious Diseases
Adrenal Hormones and Disorders

المنشورات (20)

Prevalence of reported harassment and associated mental health outcomes among medical students: a cross-sectional study in Sousse, Tunisia
2026 · Scientific Reports · استُشهد به 1 مرة
Orbital Complications and Prognosis of Acute Ethmoiditis: A Pediatric Retrospective Observational Study
2026 · Ear Nose & Throat Journal · استُشهد به 1 مرة
Evaluation of HPA Axis Function in Pediatric Patients with Chronic Corticosteroid Therapy Using the Low-Dose (1 μg) Synacthen Test
2026 · Research Square
Comprehensive analysis of copy number variations in congenital heart defects Tunisian patients: chromosomal microarray analysis insights
2026 · Molecular Cytogenetics
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
2026 · Diagnostics
Comparative phytochemical profiling, antioxidant activity, and subacute toxicity assessment of infusion and decoction extracts of pumpkin seeds
2026 · INNOSC Theranostics and Pharmacological Sciences
Case Report: Compound heterozygous ITGB2 variants causing leukocyte adhesion deficiency type I With preserved CD18 expression
2026 · Frontiers in Immunology
Clinical and genomic characterization of corpus callosum abnormalities (CCA) in 107 Tunisian patients using a stepwise diagnostic approach
2026 · Frontiers in Genetics
Management of pediatric acute mastoiditis: A single-center experience over two decades
2025 · Biomedicine & Healthcare Research
Mitochondrial genes modulate the phenotypic expression of congenital scoliosis syndrome caused by mutations in the TBXT gene
2024 · Gene · استُشهد به 2 مرة
Recurrent pneumococcal meningitis in children: Diagnostic dilemma.
2024 · PubMed
Paediatric critical COVID-19: clinical features and outcomes during five waves.
2022 · Zenodo (CERN European Organization for Nuclear Research) · استُشهد به 1 مرة
Paediatric critical COVID-19: clinical features and outcomes during five waves.
2022 · F1000Research
Bilateral pheochromocytoma revealed by acute abdominal pain in a child. A case report
2020 · Pediatric Endocrinology Diabetes and Metabolism · استُشهد به 1 مرة
Acute appendicitis complicating pregnancy: a 33 case series, diagnosis and management features, maternal and neonatal outcomes
2018 · Pan African Medical Journal · استُشهد به 25 مرة
Malignant hyperthermia in a 4-year-old girl during anesthesia induction with sevoflurane and succinylcholine for congenital ptosis surgery
2018 · Saudi Journal of Ophthalmology · استُشهد به 5 مرة
Clinical, Molecular, and Computational Analysis in two cases with mitochondrial encephalomyopathy associated with SUCLG1 mutation in a consanguineous family
2017 · Biochemical and Biophysical Research Communications · استُشهد به 10 مرة
Hypomagnesemia with Secondary Hypocalcemia Linked to a Novel TRPM6 Gene Mutation
2016 · Open Journal of Pediatrics · استُشهد به 3 مرة
Whole mitochondrial genome analysis in two families with dilated mitochondrial cardiomyopathy: detection of mutations in MT-ND2 and MT-TL1 genes
2015 · Mitochondrial DNA Part A · استُشهد به 13 مرة
Chediak–Higashi Syndrome Presented as Accelerated Phase: Case Report and Review of the Literature
2014 · Indian Journal of Hematology and Blood Transfusion · استُشهد به 9 مرة

مجلات النشر

Scientific Reports × 1
Ear Nose & Throat Journal × 1
Research Square × 1
Molecular Cytogenetics × 1
Diagnostics × 1
INNOSC Theranostics and Pharmacological Sciences × 1

المنشورات حسب السنة

20268
20251
20242
20222
20201
20182
20171
20161
20151
20141

التعاون العلمي

المؤسسات الشريكة : University of Sfax · Hôpital Sahloul · Faculty of Medicine of Sfax · Faculty of Sciences of Sfax · University of Kairouan

المؤلفون المشاركون

البيانات البيبليوغرافية مصدرها OpenAlex (قاعدة مفتوحة).