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Abir Zioudi
Observed names:
Zioudi Abir,
Zioudi, Abir
Institutions:
Tunis University,
National Institute of Neurology Mongi-Ben Hamida,
Faculté de médecine de Tunis,
Tunis El Manar University
Observed institutions:
Tunis University,
National Institute of Neurology Mongi-Ben Hamida,
Faculté de médecine de Tunis,
Tunis El Manar University
ORCID:
0009-0000-6705-6461
Observed ORCID:
0009-0000-6705-6461
OpenAlex ID:
A5008991270
Subacute Sclerosing Panencephalitis in a North African Cohort: Findings From the Post-Measles Epidemic Era
2025
·
Meriem Ben Hafsa
, Zouhour Miladi
, et al.
·
Sage Open Pediatrics
·
4
Expanding the genetic spectrum of mitochondrial diseases in Tunisia: novel variants revealed by whole-exome sequencing
2024
·
Ismail Gouiza
, Meriem Hechmi
, et al.
·
Frontiers in Genetics
·
4
PDF
Biotinidase Deficiency: Report of a Tunisian Case With Neuromyelitis Optica‐Like Presentation and Review of the Literature
2025
·
Abir Zioudi
, Hanene Benrhouma
, et al.
·
Case Reports in Neurological Medicine
·
2
PDF
A Tunisian POLG mutation expands the clinical spectrum of POLG-related disorders
2025
·
Abir Zioudi
, Ismail Gouiza
, et al.
·
Mitochondrion
·
1
Efficacy and Safety of Rituximab in Children with Multiple Sclerosis: A Tunisian Retrospective Study
2026
·
Maryam Mezhoud
, Thouraya Ben Younes
, et al.
·
Multiple Sclerosis and Related Disorders
Peripheral Facial Palsy in Pediatric-Onset Multiple Sclerosis
2026
·
Fawez Dridi
, Maha Jamoussi
, et al.
·
Multiple Sclerosis and Related Disorders
Integrated exome and mitochondrial genome sequencing reveals the genetic landscape of primary mitochondrial diseases: findings from a large Tunisian cohort
2026
·
Ismail Gouiza
, Aymane Bouzidi
, et al.
·
Mitochondrion
PDF
Manifestations neurologiques dans les hémopathies malignes : étude descriptive d’une série pédiatrique
2026
·
Imen Jlidi
, Abir Zioudi
, et al.
·
Revue Neurologique
A founder variant in Tunisian PMM2-CDG patients: An integrated clinical, radiological, biochemical, and genetic study
2026
·
Lilia Kraoua
, Thouraya Ben Younes
, et al.
·
Molecular Genetics and Metabolism
Epilepsy of infancy with migrating focal seizures: Clinical, electrophysiological spectrum and genetic findings in pediatric Tunisian cases
2025
·
Aicha Kalfat
, Zouhour Miladi
, et al.
·
Journal of the Neurological Sciences
Hereditary channelopathies with central neurological manifestations: A descriptive study of a pediatric cohort
2025
·
Mohamed Slim Majoul
, Abir Zioudi
, et al.
·
Journal of the Neurological Sciences
Exploring the genetic landscape of neonatal epilepsies: Insights from a Tunisian cohort
2025
·
Aicha Kalfat
, Zouhour Miladi
, et al.
·
Journal of the Neurological Sciences
Movement disorders in subacute sclerosing panencephalitis a study of a Tunisian pediatric cohort
2025
·
Cyrine Karray
, Zouhour Miladi
, et al.
·
Journal of the Neurological Sciences
Aicardi syndrome: Clinical and paraclinical findings in Tunisian cases
2025
·
Elyes Cherif
, Zouhour Miladi
, et al.
·
Journal of the Neurological Sciences
Fluctuating ptosis revealing a blister-like intracranial aneurysm a rare diagnostic challenge
2025
·
Cyrine Karray
, Thouraya Ben Younes
, et al.
·
Journal of the Neurological Sciences
Facteurs associés au pronostic des accidents vasculaires ischémiques de l’enfant
2025
·
Meriem Ben Hafsa
, Hanen Ben Rhouma
, et al.
·
Revue Neurologique
Déficit intracérébral en créatine : étude descriptive d’une série pédiatrique
2025
·
Mohamed Slim Majoul
, Abir Zioudi
, et al.
·
Revue Neurologique
Évaluation de la qualité de vie dans la paralysie cérébrale : étude d’une cohorte pédiatrique
2025
·
Meriem Ben Hafsa
, Hanen Ben Rhouma
, et al.
·
Revue Neurologique
Syndrome de Joubert : étude épidémiologique, clinique, radiologique et génétique d’une série pédiatrique tunisienne
2025
·
Aicha Kalfat
, Hedia Klaa
, et al.
·
Revue Neurologique
Étude génétique chez les patients atteints de dystrophie musculaire de Duchenne
2025
·
Yosr Kooli
, Thouraya Ben Younes
, et al.
·
Revue Neurologique
Les paraplégies spastiques héréditaires : étude d’une cohorte pédiatrique
2025
·
Sahar Chnitir
, Hanen Ben Rhouma
, et al.
·
Revue Neurologique
Troubles du spectre de l’autisme dans les maladies héréditaires du métabolisme
2025
·
Zouhour Miladi
, Meriem Ben Hafsa
, et al.
·
Revue Neurologique
Implication of mitochondrial pyruvate carrier (MPC) in the transport of ketone bodies: New evidence provided by in silico tools
2025
·
Othmen Bacha
, Said Galai
, et al.
·
In Silico Research in Biomedicine
126. Familial Pediatric Onset Multiple Sclerosis: A Retrospective Single-Center Observational Study
2024
·
Mohamed Slim Majoul
, Abir Zioudi
, et al.
·
Multiple Sclerosis and Related Disorders
Acute Cerebellitis in Children: A Tunisian Case Series
2024
·
Yasmine Saad
, Hanene Ben Rhouma
, et al.
·
Neurology
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Works count:
47
Citation count:
11
H-index:
2
I10-index:
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