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Disruptions of neurological services, its causes and mitigation strategies during COVID-19: a global review

Journal of neurology, 2021-11, Vol.268 (11), p.3947-3960

2021

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Case report: Compound heterozygous variants detected by next-generation sequencing in a Tunisian child with ataxia-telangiectasia

Frontiers in neurology, 2024-05, Vol.15, p.1344018-1344018

2024

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First report of Tunisian patients with CDKL5‐related encephalopathy

Epilepsia open, 2024-06, Vol.9 (3), p.906-917

2024

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Customized targeted massively parallel sequencing enables the identification of novel pathogenic variants in Tunisian patients with developmental and epileptic encephalopathy

Epilepsia open, 2024-07

2024

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Complex genotypes in family with metachromatic leukodystrophy: Effect of trans and cis mutations distribution on the phenotype variability

International journal of developmental neuroscience, 2024-02, Vol.84 (1), p.35-46

2024

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Timing of referral to evaluate for epilepsy surgery: Expert Consensus Recommendations from the Surgical Therapies Commission of the International League Against Epilepsy

Epilepsia (Copenhagen), 2022-10, Vol.63 (10), p.2491-2506

2022

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Knowledge and attitudes toward epilepsy among people in Sfax region, Tunisia

Epilepsy & behavior, 2021-09, Vol.122, p.108151-108151, Article 108151

2021

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Characterization of a missense variant in COG5 in a Tunisian patient with COG5-CDG syndrome and insights into the effect of non-synonymous variants on COG5 protein

Journal of human genetics, 2024-07

2024

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Global survey on disruption and mitigation of neurological services during COVID-19: the perspective of global international neurological patients and scientific associations

Journal of neurology, 2022-01, Vol.269 (1), p.26-38

2022

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A new case with the recurrent PURA p.(Phe233del) pathogenic variant: Expansion of the phenotype and review of the literature

International journal of developmental neuroscience, 2023-06, Vol.83 (4), p.383-395

2023

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Acute Demyelinating Syndromes: A report of child neurology department of Sfax University Hospital

Multiple sclerosis and related disorders, 2021-11, Vol.56, p.103291-103291, Article 103291

2021

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Case report: Functional analysis of the p.Arg507Trp variant of the PIGT gene supporting the moderate epilepsy phenotype of mutations in the C-terminal region

Frontiers in neurology, 2023-03, Vol.14, p.1092887

2023

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Lessons learned from COVID-19 impact of pandemic on children with neurological disorders in Sfax, Tunisia

International journal of public health science, 2023-03, Vol.12 (1), p.239

2023

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Clinical and genetic aspect of 30 tunisian families with febrile seizures

Tunisie Medicale, 2019-04, Vol.97 (4), p.525-532

2019

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Safety and efficacy of teriflunomide in paediatric multiple sclerosis (TERIKIDS): a multicentre, double-blind, phase 3, randomised, placebo-controlled trial

Lancet neurology, 2021-12, Vol.20 (12), p.1001-1011

2021

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Juvenile Dermatomyositis Without Skin Lesions in an Antinuclear Matrix Protein 2 Antibody Seropositive Pediatric Case

Journal of clinical neuromuscular disease, 2023-09, Vol.25 (1), p.46-50

2023

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Combined in Silico Prediction Methods, Molecular Dynamic Simulation, and Molecular Docking of FOXG1 Missense Mutations: Effect on FoxG1 Structure and Its Interactions with DNA and Bmi-1 Protein

Journal of molecular neuroscience, 2022-08, Vol.72 (8), p.1695-1705

2022

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Unusual double mutation in MECP2 and CDKL5 genes in Rett-like syndrome: Correlation with phenotype and genes expression

Clinica chimica acta, 2020-09, Vol.508, p.287-294

2020

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Challenges to associate early onset epilepsy with COVID-19 autoimmune encephalitis: A case report

World journal of immunology, 2023-05, Vol.13 (1), p.1-10

2023

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Epilepsy Pioneers in Tunisia and Current Educational Programs in Tunisia

Journal of pediatric epilepsy, 2019-03, Vol.8 (1), p.19-20

2019

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Primary intestinal lymphangiectasia associated to epilepsy: a case report

PAMJ clinical medicine, 2021, Vol.6

2021

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Drug-Resistant Myoclonic Epilepsy Revealing Juvenile Huntington's Disease: A Case Report

Journal of pediatric epilepsy, 2018-03, Vol.7 (1), p.21-23

2018

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Position Statement:Emerging genetic therapies for rare disorders: Genetic therapies

Journal of the International Child Neurology Association, 2019-07

2019

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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

Journal of human genetics, 2014-04, Vol.59 (4), p.216-222

2014

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Disruptions of neurological services, its causes and mitigation strategies during COVID-19: a global review

Case report: Compound heterozygous variants detected by next-generation sequencing in a Tunisian child with ataxia-telangiectasia

First report of Tunisian patients with CDKL5‐related encephalopathy

Customized targeted massively parallel sequencing enables the identification of novel pathogenic variants in Tunisian patients with developmental and epileptic encephalopathy

Complex genotypes in family with metachromatic leukodystrophy: Effect of trans and cis mutations distribution on the phenotype variability

Timing of referral to evaluate for epilepsy surgery: Expert Consensus Recommendations from the Surgical Therapies Commission of the International League Against Epilepsy

Treatment of seizures in the neonate: Guidelines and consensus‐based recommendations—Special report from the ILAE Task Force on Neonatal Seizures

Knowledge and attitudes toward epilepsy among people in Sfax region, Tunisia

Characterization of a missense variant in COG5 in a Tunisian patient with COG5-CDG syndrome and insights into the effect of non-synonymous variants on COG5 protein

Global survey on disruption and mitigation of neurological services during COVID-19: the perspective of global international neurological patients and scientific associations

A new case with the recurrent PURA p.(Phe233del) pathogenic variant: Expansion of the phenotype and review of the literature

Acute Demyelinating Syndromes: A report of child neurology department of Sfax University Hospital

Case report: Functional analysis of the p.Arg507Trp variant of the PIGT gene supporting the moderate epilepsy phenotype of mutations in the C-terminal region

Lessons learned from COVID-19 impact of pandemic on children with neurological disorders in Sfax, Tunisia

Clinical and genetic aspect of 30 tunisian families with febrile seizures

Safety and efficacy of teriflunomide in paediatric multiple sclerosis (TERIKIDS): a multicentre, double-blind, phase 3, randomised, placebo-controlled trial

Juvenile Dermatomyositis Without Skin Lesions in an Antinuclear Matrix Protein 2 Antibody Seropositive Pediatric Case

Combined in Silico Prediction Methods, Molecular Dynamic Simulation, and Molecular Docking of FOXG1 Missense Mutations: Effect on FoxG1 Structure and Its Interactions with DNA and Bmi-1 Protein

Unusual double mutation in MECP2 and CDKL5 genes in Rett-like syndrome: Correlation with phenotype and genes expression

Challenges to associate early onset epilepsy with COVID-19 autoimmune encephalitis: A case report

Epilepsy Pioneers in Tunisia and Current Educational Programs in Tunisia

Primary intestinal lymphangiectasia associated to epilepsy: a case report

Drug-Resistant Myoclonic Epilepsy Revealing Juvenile Huntington's Disease: A Case Report

Position Statement:Emerging genetic therapies for rare disorders: Genetic therapies

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

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