Publications by authors named "Emna Ellouz"

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Artificial intelligence-driven eye tracker models for Alzheimer's disease diagnosis: A systematic review and meta-analysis.
Imen Ketata, Emna Ellouz

J Alzheimers Dis· December 2025

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Exploring Optic Glioma and Type 1 Neurofibromatosis: A Literature Review of Case Reports.
Emna Ellouz, Imen Ketata, Rahma Kchaou

Neuroophthalmology· December 2025

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Burden of migraine among university students in the Middle East and North Africa: a cross-sectional study of prevalence, mental health comorbidities, and disability.
Ahmed Amir Samir, Ahmed Samy Elgammal, Abdelrhman Mahmoud Alieldeen, Eman Gomaa Allam, Imen Ketata, Emna Ellouz

BMC Public Health· October 2025

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Psychoses in Pediatric-Onset Multiple Sclerosis: A Case Report and Systematic Review.
Emna Ellouz, Imen Ketata, Wafa Abbes, Hend Gargouri, Sondes Bader

J Child Adolesc Psychiatr Nurs· November 2024

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From pathological mechanisms in Krabbe disease to cutting-edge therapy: A comprehensive review.
Imen Ketata, Emna Ellouz

Neuropathology· August 2024

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Impact of prenatal, neonatal, and postnatal factors on epilepsy risk in children and adolescents: a systematic review and meta-analysis.
Imen Ketata, Emna Ellouz, Rahil Mizouri

Acta Epileptol· January 2024

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Phenotypic variability in a Tunisian family with X-linked adrenoleukodystrophy caused by the p.Gln316Pro novel mutation.
Fakhri Kallabi, Emna Ellouz, Mouna Tabebi, Ghada Ben Salah, Naziha Kaabechi

Clin Chim Acta· January 2016

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Founder effect confirmation of c.241A>G mutation in the L2HGDH gene and characterization of oxidative stress parameters in six Tunisian families with L-2-hydroxyglutaric aciduria.
Nadege Kammoun Jellouli, Ikhlass Hadj Salem, Emna Ellouz, Zeineb Kamoun, Fatma kamoun

J Hum Genet· April 2014

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[Study of a Tunisian population of children with learning disorders].
Ines Hsairi Guidara, Ines Ayadi, Emna Ellouz, Imen Abid, Fatma Kamoun

Tunis Med· June 2013

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Molecular confirmation of founder mutation c.-167A>G in Tunisian patients with PMLD disease.
Nadege Kammoun Jellouli, Ikhlass Hadj Salem, Emna Ellouz, Nacim Louhichi, Abdelaziz tlili

Gene· January 2013

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Frontal motor seizure following non-convulsive status epilepticus in ring chromosome 20 syndrome.
Fatma F Kamoun, Emna J Ellouz, Ines G Hsairi, Chahnez C Triki

Neurosciences (Riyadh)· January 2012

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