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Ilhem Ben Youssef-Turki

Observed names: I Ben Youssef-Turki, I. Ben Youssef-Turki, I. Youssef-Turki, Ilhem Ben Youssef, Ilhem Ben Youssef Turki, Ilhem Ben Youssef‐Turki, Ilhem Ben Youssef–Turki, Ilhem BenYoussef-Turki, Ilhem BenYoussef‐Turki, Ilhem Benyoussef Turki, Ilhem Benyoussef-Turki, Ilhem Turki, Ilhem Turki Ben Youssef, Ilhem Youssef, Ilhem Youssef-Turki, Ilhem Ben Youssef‐Turki, Turki Ilhem
Observed institutions: Tunis University, Radboud University Medical Center, National Institute of Neurology Mongi-Ben Hamida, Hôpital Razi de La Manouba, Faculté de médecine de Tunis, Tunis El Manar University
ORCID: 0000-0002-4994-9925
Observed ORCID: 0000-0002-4994-9925
OpenAlex ID: A5085786084
Severe dysautonomia as a main feature of anti-GAD encephalitis: Report of a paediatric case and literature review
2018 · Nedia Ben Achour, Thouraya Ben Younes, et al. · European Journal of Paediatric Neurology · 42
MPC2 variants disrupt mitochondrial pyruvate metabolism and cause an early-onset mitochondriopathy
2022 · Claire Pujol, Elise Lebigot, et al. · Brain · 23
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Methylmalonic acidemia and hyperglycemia: An unusual association
2011 · Marouani Imen, Benrhouma Hanene, et al. · Brain and Development · 19
Homozygous 2p11.2 deletion supports the implication of ELMOD3 in hearing loss and reveals the potential association of CAPG with ASD/ID etiology
2018 · Saida Lahbib, Claire S. Leblond, et al. · Journal of Applied Genetics · 15
Postencephalitic parkinsonism and selective involvement of substantia nigra in childhood
2014 · Ibtihel Rebai, Hanene Ben Rhouma, et al. · Brain and Development · 13
Muscle-Specific Kinase Autoimmune Myasthenia Gravis: Report of a Pediatric Case and Literature Review
2018 · Hanene Benrhouma, Hedia Klaa, et al. · Neuropediatrics · 10
RTN2 deficiency results in an autosomal recessive distal motor neuropathy with lower limb spasticity
2024 · Reza Maroofian, Payam Sarraf, et al. · Brain · 8
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Early Life Epilepsy and Episodic Apnea Revealing an ATP1A3 Mutation: Report of a Pediatric Case and Literature Review
2018 · Hanene Benrhouma, Hedia Klaa, et al. · Neuropediatrics · 8
Chronic Inflammatory Demyelinating Polyradiculoneuropathy in Children
2006 · I Ben Youssef-Turki, A Kraoua, et al. · Neuropediatrics · 8
Next-generation sequencing of Tunisian Leigh syndrome patients reveals novel variations: impact for diagnosis and treatment
2022 · Meriem Hechmi, Majida Charif, et al. · Bioscience Reports · 7
Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment
2021 · Rahma Mkaouar, Zied Riahi, et al. · PLoS ONE · 7
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Pyridoxine-dependent epilepsy: A novel mutation in a Tunisian child
2017 · T. Ben Younes, I. Kraoua, et al. · Archives de Pédiatrie · 7
Clinical and Biochemical Profile of Tyrosinemia Type 1 in Tunisia
2015 · Fahmi Nasrallah, Mohamed Hammami, et al. · Clinical Laboratory · 6
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
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Hypomyelination and Congenital Cataract: Clinical, Imaging, and Genetic Findings in Three Tunisian Families and Literature Review
2021 · Yosra Bouyacoub, Cyrine Drissi, et al. · Neuropediatrics · 4
Rasmussen’s Encephalitis: A Report of a Tunisian Pediatric Case and Literature Review
2020 · Hedia Klaa, Thouraya Ben Younes, et al. · Case Reports in Neurological Medicine · 4
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Epilepsy Aspects and EEG Patterns in Neuro-Metabolic Diseases
2011 · Ilhem Ben Youssef-Turki, Ichraf Kraoua, et al. · Journal of Behavioral and Brain Science · 4
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L’acidurie glutarique type I : une cause méconnue de dystonie progressive
2006 · N. Gouider-Khouja, I. Ben Youssef-Turki · Revue Neurologique · 4
Pediatric Neurotuberculosis: A cases series and review of the literature
2023 · Maha Jamoussi, Hanene Benrhouma, et al. · European Journal of Paediatric Neurology · 3
Neuronal ceroïd‐lipofuscinosis: Clinical, electroencephalographic, imaging, and genetic study of a maghrebian series
2022 · Thouraya Ben Younes, Ichraf Kraoua, et al. · Clinical Genetics · 3
Farber disease: A Fatal Childhood Disorder with Nervous System Involvement
2020 · Ichraf Kraoua, Thouraya Ben Younes, et al. · Journal of Rare Diseases Research & Treatment · 3
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A Case of Progressive Chorea Resulting From GLUT 1 Deficiency
2015 · Ichraf Kraoua, Hanene Benrhouma, et al. · Movement Disorders Clinical Practice · 3
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Ophtalmoplégie douloureuse récidivante : migraine ophtalmoplégique ou schwannome du nerf oculomoteur ?
2014 · A. Riahi, I. Ben Youssef-Turki, et al. · Pratique Neurologique - FMC · 3
Profiles of Monocyte Subsets and Fibrosis-Related Genes in Patients with Muscular Dystrophy Undergoing Intermittent Prednisone Therapy
2025 · Asma Chikhaoui, Dorra Najjar, et al. · International Journal of Molecular Sciences · 2
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
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Works count: 104
Citation count: 232
H-index: 8
I10-index: 6
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