Author

Ilhem Turki

Observed names: Ben Youssef Turki, Ilhem, I Turki, I. Ben Youssef Turki, I. Ben Youssef –Turki, I. Turki, Ilhem B. Y. Turki, Ilhem Ben Youssef Turki, Ilhem Ben Youssef-Turki, Ilhem Ben-Youssef Turki, Ilhem Youssef Turki, Turki, I., Turki, Ilhem

Institution: Hôpital La Rabta

Observed institutions: Tunis University, Hôpital La Rabta, Wolters Kluwer Health, National Institute of Neurology Mongi-Ben Hamida, Bicêtre Hospital, Faculté de médecine de Tunis, Tunis El Manar University

ORCID: 0000-0003-2644-3128

Observed ORCID: 0000-0003-2644-3128

OpenAlex ID: A5113875544

AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders

2019 · Vincenzo Salpietro, Christine L. Dixon, et al. · Nature Communications · 252

Effect of vitamin E supplementation in patients with ataxia with vitamin E deficiency

2001 · S. Gabsi, N. Gouider‐Khouja, et al. · European Journal of Neurology · 148

Phenotypic Features and Genetic Findings in Sacsin-Related Autosomal Recessive Ataxia in Tunisia

2003 · Ghada El Euch-Fayache, Irfan Lalani, et al. · Archives of Neurology · 110

Relationship between ABCB1 3435TT genotype and antiepileptic drugs resistance in Epilepsy: updated systematic review and meta-analysis

2017 · Malek Chouchi, Wajih Kaabachi, et al. · BMC Neurology · 81

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Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxia in a Tunisian family

2000 · N. Mrissa, S. Belal, et al. · Neurology · 80

Electrophysiological and nerve biopsy: comparative study in Friedreich's ataxia and Friedreich's ataxia phenotype with vitamin E deficiency

1998 · M Zouari, M Feki, et al. · Neuromuscular Disorders · 67

ABCB1 Polymorphisms and Drug-Resistant Epilepsy in a Tunisian Population

2019 · Malek Chouchi, Hedia Klaa, et al. · Disease Markers · 34

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Infantile and childhood onset PLA 2G6‐associated neurodegeneration in a large North African cohort

2014 · M. Romani, I. Kraoua, et al. · European Journal of Neurology · 34

Status dystonicus in childhood.

2015 · Nahla Touati, Hanène Ben Rhouma, et al. · PubMed · 24

Anti-Ma2-encephalitis in a 2 year-old child: A newly diagnosed case and literature review

2015 · Saloua Mrabet, Nedia Ben Achour, et al. · European Journal of Paediatric Neurology · 20

Germline homozygous missense DEPDC5 variants cause severe refractory early-onset epilepsy, macrocephaly and bilateral polymicrogyria

2022 · Athina Ververi, Sara Zagaglia, et al. · Human Molecular Genetics · 18

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Heterogeneous clinical features in Cockayne syndrome patients and siblings carrying the same CSA mutations

2022 · Asma Chikhaoui, Ichraf Kraoua, et al. · Orphanet Journal of Rare Diseases · 14

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Plasma GM2 Ganglioside Potential Biomarker for Diagnosis, Prognosis and Disease Monitoring of GM2-Gangliosidosis

2022 · Amélie Blondel, Ichraf Kraoua, et al. · SSRN Electronic Journal · 14

Autoimmune Encephalitis in Tunisia: Report of a Pediatric Cohort

2021 · Bissene Douma, Thouraya Ben Younes, et al. · Journal of Immunology Research · 13

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Pediatric Multiple Sclerosis in Tunisia: A Retrospective Study over 11 Years

2017 · Nedia Ben Achour, Ibtihel Rebai, et al. · BioMed Research International · 13

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Fourth meeting of the European Neurological Society 25–29 June 1994 Barcelona, Spain

1994 · The European Velnacrine Study Group, L. Harms, et al. · Journal of Neurology · 13

Childhood opsoclonus–myoclonus syndrome: A case series from Tunisia

2017 · Nedia Ben Achour, Saloua Mrabet, et al. · Brain and Development · 12

Mixed movements disorders as an initial feature of pediatric lupus

2015 · Saloua Mrabet, Hanene Benrhouma, et al. · Brain and Development · 11

Immunity in the Progeroid Model of Cockayne Syndrome: Biomarkers of Pathological Aging

2024 · Khouloud Zayoud, Asma Chikhaoui, et al. · Cells · 10

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Identification and Characterization of a Novel Recurrent ERCC6 Variant in Patients with a Severe Form of Cockayne Syndrome B

2021 · Khouloud Zayoud, Ichraf Kraoua, et al. · Genes · 10

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Duchenne muscular dystrophy in Tunisia: A clinical and morphological study of 77 cases

1992 · Mongi Ben Hamida, Najoua Miladi, et al. · Journal of the Neurological Sciences · 10

Sanfilippo Disease, Type C: Three Cases in the Same Family

1989 · I. Turki, H. Kresse, et al. · Neuropediatrics · 10

Seronegative myasthenia gravis with bladder dysfunction

2012 · I. Marouani, I. Kraoua, et al. · Revue Neurologique · 9

Nonketotic Hyperglycinemia in Tunisia. Report upon a Series of 69 Patients

2020 · Fahmi Nasrallah, Sameh Hadj-Taieb, et al. · Neuropediatrics · 8

Clinical and genetic spectrum of Ataxia Telangiectasia Tunisian patients: Bioinformatic analysis unveil mechanisms of ATM variants pathogenicity

2024 · Rim Jenni, Hedia Klaa, et al. · International Journal of Biological Macromolecules · 5

Works count: 131

Citation count: 1,074

H-index: 13

I10-index: 22