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Methylmalonic acidemia and hyperglycemia: An unusual association

Brain & development (Tokyo. 1979), 2012-02, Vol.34 (2), p.113-114

2012

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Reply to Dr. Suresh Kumar

Brain & development (Tokyo. 1979), 2013-02, Vol.35 (2), p.186-186

2013

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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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Clinical and molecular characterization of 1q43q44 deletion and corpus callosum malformations: 2 new cases and literature review

Molecular cytogenetics, 2022-10, Vol.15 (1), p.1-42, Article 42

2022

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Eye movements in parkinsonian syndromes

Annals of neurology, 1994-04, Vol.35 (4), p.420-426

1994

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Clinicogenetic study of mutations in LRRK2 exon 41 in Parkinson's disease patients from 18 countries

Movement disorders, 2006-08, Vol.21 (8), p.1102-1108

2006

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Lesch Nyhan syndrome: A novel complex mutation in a Tunisian child

Brain & development (Tokyo. 1979), 2014-11, Vol.36 (10), p.921-923

2014

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Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study

Parkinsonism & related disorders, 2003-06, Vol.9 (5), p.247-251

2003

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Subcutaneous Interferon Beta-1a in Pediatric Multiple Sclerosis: A Retrospective Study

Journal of child neurology, 2013-07, Vol.28 (7), p.849-856

2013

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Subcutaneous interferon β-1a in pediatric patients with multiple sclerosis: Regional differences in clinical features, disease management, and treatment outcomes in an international retrospective study

Journal of the neurological sciences, 2016-04, Vol.363, p.33-38

2016

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Évaluation par les neurologues et les patients de DigiPark, une application dédiée à la télésurveillance (TS) de la maladie de Parkinson (MP)

Revue neurologique, 2024-04, Vol.180, p.S19-S19

2024

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Wilson's disease

Parkinsonism & related disorders, 2009-12, Vol.15, p.S126-S129

Gouider-Khouja, Neziha

2009

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Clinicogenetic study of mutations inLRRK2 exon 41 in Parkinson's disease patients from 18 countries

Movement disorders, 2006-08, Vol.21 (8), p.1102-1108

2006

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"Pure" striatonigral degeneration and Parkinson's disease: A comparative clinical study

Movement disorders, 1995-05, Vol.10 (3), p.288-294

1995

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First report of an unusual novel double mutation affecting the transcription repression domain of MeCP2 and causing a severe phenotype of Rett syndrome: Molecular analyses and computational investigation

Biochemical and biophysical research communications, 2018-02, Vol.497 (1), p.93-101

2018

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Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome

Orphanet journal of rare diseases, 2014-05, Vol.9 (1), p.72-72, Article 72

2014

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3-Phosphoglycerate dehydrogenase deficiency: description of two new cases in Tunisia and review of the literature

Neuropediatrics, 2013-10, Vol.44 (5), p.281

2013

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Particularités du traitement des dystonies focales par la Toxine Botulique : étude descriptive sur 8 ans

Revue neurologique, 2017-03, Vol.173, p.S148-S149

2017

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Movement disorders in neuro-metabolic diseases

European journal of paediatric neurology, 2010-07, Vol.14 (4), p.304-307

2010

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Status dystonicus in childhood

Tunisie Medicale, 2015-12, Vol.93 (12), p.756-759

2015

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Clinical and genetic study of familial Parkinson's disease in Tunisia

Neurology, 2000-04, Vol.54 (8), p.1603

2000

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Neuro-imagerie des maladies lysosomales

Revue neurologique, 2012-04, Vol.168, p.A113-A113

2012

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Corrélation électro-clinique de l’EEG dans l’épilepsie et les mouvements anormaux : étude rétrospective sur 4150 EEG (2005–2009)

Revue neurologique, 2012-04, Vol.168, p.A125-A126

2012

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Encéphalite rubéolique : observation récente d’une fréquence inhabituelle

Revue neurologique, 2012-04, Vol.168, p.A131-A131

2012

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Methylmalonic acidemia and hyperglycemia: An unusual association

Reply to Dr. Suresh Kumar

Postencephalitic parkinsonism and selective involvement of substantia nigra in childhood

Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease families

Clinical and molecular characterization of 1q43q44 deletion and corpus callosum malformations: 2 new cases and literature review

Eye movements in parkinsonian syndromes

Clinicogenetic study of mutations in LRRK2 exon 41 in Parkinson's disease patients from 18 countries

Lesch Nyhan syndrome: A novel complex mutation in a Tunisian child

Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study

Subcutaneous Interferon Beta-1a in Pediatric Multiple Sclerosis: A Retrospective Study

Subcutaneous interferon β-1a in pediatric patients with multiple sclerosis: Regional differences in clinical features, disease management, and treatment outcomes in an international retrospective study

Évaluation par les neurologues et les patients de DigiPark, une application dédiée à la télésurveillance (TS) de la maladie de Parkinson (MP)

Wilson's disease

Clinicogenetic study of mutations inLRRK2 exon 41 in Parkinson's disease patients from 18 countries

"Pure" striatonigral degeneration and Parkinson's disease: A comparative clinical study

First report of an unusual novel double mutation affecting the transcription repression domain of MeCP2 and causing a severe phenotype of Rett syndrome: Molecular analyses and computational investigation

Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome

3-Phosphoglycerate dehydrogenase deficiency: description of two new cases in Tunisia and review of the literature

Particularités du traitement des dystonies focales par la Toxine Botulique : étude descriptive sur 8 ans

Movement disorders in neuro-metabolic diseases

Status dystonicus in childhood

Clinical and genetic study of familial Parkinson's disease in Tunisia

Neuro-imagerie des maladies lysosomales

Corrélation électro-clinique de l’EEG dans l’épilepsie et les mouvements anormaux : étude rétrospective sur 4150 EEG (2005–2009)

Encéphalite rubéolique : observation récente d’une fréquence inhabituelle

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