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ABCB1 Polymorphisms and Drug-Resistant Epilepsy in a Tunisian Population

Disease markers, 2019, Vol.2019 (2019), p.1-16

2019

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

BMC neurology, 2017-02, Vol.17 (1), p.32-32, Article 32

2017

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Neuronal ceroïd‐lipofuscinosis: Clinical, electroencephalographic, imaging, and genetic study of a maghrebian series

Clinical genetics, 2022-08, Vol.102 (2), p.157-160

2022

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Postencephalitic parkinsonism and selective involvement of substantia nigra in childhood

Brain & development (Tokyo. 1979), 2015-01, Vol.37 (1), p.153-157

2015

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Childhood opsoclonus–myoclonus syndrome: A case series from Tunisia

Brain & development (Tokyo. 1979), 2017-10, Vol.39 (9), p.751-755

2017

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Tremor Ataxia With Central Hypomyelation Phenotype Related to a Recurrent POLR3A Mutation in Six Unrelated Tunisian Families

Molecular genetics & genomic medicine, 2024-10, Vol.12 (10), p.e70007-n/a

2024

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Homozygous 2p11.2 deletion supports the implication of ELMOD3 in hearing loss and reveals the potential association of CAPG with ASD/ID etiology

Journal of applied genetics, 2019-02, Vol.60 (1), p.49-56

2019

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Rasmussen’s Encephalitis: A Report of a Tunisian Pediatric Case and Literature Review

Case reports in neurological medicine, 2020-06, Vol.2020 (2020), p.1-5

2020

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

Human molecular genetics, 2023-01, Vol.32 (4), p.580-594

2023

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Next-generation sequencing of Tunisian Leigh syndrome patients reveals novel variations: impact for diagnosis and treatment

Bioscience reports, 2022-09, Vol.42 (9), p.1

2022

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Expanding the genetic spectrum of mitochondrial diseases in Tunisia: novel variants revealed by whole-exome sequencing

Frontiers in genetics, 2024-01, Vol.14 (5), p.1259826

2024

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Hypomyelination and Congenital Cataract: Clinical, Imaging, and Genetic Findings in Three Tunisian Families and Literature Review

Neuropediatrics, 2021-08, Vol.52 (4), p.302-309

2021

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Autoimmune Encephalitis in Tunisia: Report of a Pediatric Cohort

Journal of Immunology Research, 2021, Vol.2021, p.6666117-7

2021

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Severe dysautonomia as a main feature of anti-GAD encephalitis: Report of a paediatric case and literature review

European journal of paediatric neurology, 2018-05, Vol.22 (3), p.548-551

2018

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

BioMed research international, 2017-01, Vol.2017 (2017), p.1-8

2017

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A Case of Progressive Chorea Resulting From GLUT1 Deficiency

Movement disorders clinical practice (Hoboken, N.J.), 2015-12, Vol.2 (4), p.424-425

2015

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

European journal of paediatric neurology, 2015-11, Vol.19 (6), p.737-742

2015

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Early Life Epilepsy and Episodic Apnea Revealing an ATP1A3 Mutation: Report of a Pediatric Case and Literature Review

Neuropediatrics, 2018-10, Vol.49 (5), p.339-341

2018

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Letter to the editor: “A case of Guillain-Barré syndrome with meningeal irritation”

Brain & development (Tokyo. 1979), 2017-10, Vol.39 (9), p.815-815

2017

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Clinical and Biochemical Profile of Tyrosinemia Type 1 in Tunisia

Clinical laboratory (Heidelberg), 2015, Vol.61 (5-6), p.487

2015

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Genetic characterization of hypomyelinating leukodystrophies in the Tunisian cohort

Journal of the neurological sciences, 2021-10, Vol.429, p.118263, Article 118263

2021

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Pediatric MOGAD: Tunisian case series

Journal of the neurological sciences, 2023-12, Vol.455, p.121256, Article 121256

2023

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Subacute sclerosing panencephalitis: Clinical and paraclinical study of Tunisian pediatric cases

Journal of the neurological sciences, 2023-12, Vol.455, p.121255, Article 121255

2023

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ABCB1 Polymorphisms and Drug-Resistant Epilepsy in a Tunisian Population

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

Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment

Neuronal ceroïd‐lipofuscinosis: Clinical, electroencephalographic, imaging, and genetic study of a maghrebian series

Postencephalitic parkinsonism and selective involvement of substantia nigra in childhood

Childhood opsoclonus–myoclonus syndrome: A case series from Tunisia

Tremor Ataxia With Central Hypomyelation Phenotype Related to a Recurrent POLR3A Mutation in Six Unrelated Tunisian Families

Homozygous 2p11.2 deletion supports the implication of ELMOD3 in hearing loss and reveals the potential association of CAPG with ASD/ID etiology

Rasmussen’s Encephalitis: A Report of a Tunisian Pediatric Case and Literature Review

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

Next-generation sequencing of Tunisian Leigh syndrome patients reveals novel variations: impact for diagnosis and treatment

Expanding the genetic spectrum of mitochondrial diseases in Tunisia: novel variants revealed by whole-exome sequencing

Hypomyelination and Congenital Cataract: Clinical, Imaging, and Genetic Findings in Three Tunisian Families and Literature Review

Autoimmune Encephalitis in Tunisia: Report of a Pediatric Cohort

Severe dysautonomia as a main feature of anti-GAD encephalitis: Report of a paediatric case and literature review

RTN2 deficiency results in an autosomal recessive distal motor neuropathy with lower limb spasticity

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

A Case of Progressive Chorea Resulting From GLUT1 Deficiency

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

Early Life Epilepsy and Episodic Apnea Revealing an ATP1A3 Mutation: Report of a Pediatric Case and Literature Review

Letter to the editor: “A case of Guillain-Barré syndrome with meningeal irritation”

Clinical and Biochemical Profile of Tyrosinemia Type 1 in Tunisia

Genetic characterization of hypomyelinating leukodystrophies in the Tunisian cohort

Pediatric MOGAD: Tunisian case series

Subacute sclerosing panencephalitis: Clinical and paraclinical study of Tunisian pediatric cases

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