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Author Details

Ali Benomar
Medical School and Pharmacy, University Mohammed V in Rabat
1994
107
28
Trey Ideker (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
37256495Gene Panel Sequencing Analysis Revealed a Strong Contribution of Rare Coding Variants to the Risk of Parkinson's Disease in Sporadic Moroccan Patients.J Mol Neurosci2023
35337700Trends in the consumption and cost of antiepileptics in Morocco between 2008 and 2018.Rev Epidemiol Sante Publique2022
32557143Gene Panel Sequencing Identifies Novel Pathogenic Mutations in Moroccan Patients with Familial Parkinson Disease.J Mol Neurosci2021
32356711[Current antiplatelet agents, new inhibitors and therapeutic targets].Med Sci (Paris)2020
31096916Contribution of fibrin glue in the surgery of cyanogenic and non-cyanogenic congenital cardiopathies: retrospective cohort study.BMC Cardiovasc Disord2019
31303947A case of bilateral thalamic infarct complicating tuberculous meningoencephalitis.Pan Afr Med J2019
29631855Stroke and syphilis: A retrospective study of 53 patients.Rev Neurol (Paris)2018
30108543Deep Brain Stimulation in Moroccan Patients With Parkinson's Disease: The Experience of Neurology Department of Rabat.Front Neurol2018
30581635Genetic Analysis of Undiagnosed Juvenile GM1-Gangliosidosis by Microarray and Exome Sequencing.Case Rep Genet2018
29670566Non-Motor Symptoms of Parkinson's Disease and Their Impact on Quality of Life in a Cohort of Moroccan Patients.Front Neurol2018
29525037Association of vitamin D status with multiple sclerosis in a case-control study from Morocco.Rev Neurol (Paris)2018
28723952Evidence for prehistoric origins of the G2019S mutation in the North African Berber population.PLoS One2017
28320518A case of neurosyphilis presenting with essential-like tremor.Rev Neurol (Paris)2017
28465860<i>LRRK2</i> G2019S Mutation: Prevalence and Clinical Features in Moroccans with Parkinson's Disease.Parkinsons Dis2017
29163333Mutation Analysis of Consanguineous Moroccan Patients with Parkinson's Disease Combining Microarray and Gene Panel.Front Neurol2017
26867662Vitamin D deficiency and its role in neurological conditions: A review.Rev Neurol (Paris)2016
27413743A Novel Homozygous p.L539F Mutation Identified in PINK1 Gene in a Moroccan Patient with Parkinsonism.Biomed Res Int2016
27259058Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia.Am J Hum Genet2016
27283293Cost of Treatment of Cerebral Aneurysm Embolization: Study of Associated Factors.Neurol Ther2016
27153400Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia.Am J Hum Genet2016
25732939Measles in Morocco: epidemiological profile and impact of vaccination strategy.Adv Ther2015
26644099[Clinical and environmental aspects of amyotrophic lateral sclerosis in moroccan population: a study of 60 cases].Tunis Med2015
26608566[Pathological and clinical correlations in renal AA amyloidosis: A Moroccan series of 30 cases].Nephrol Ther2015
26958025Clinical and genetic data of Huntington disease in Moroccan patients.Afr Health Sci2015
25896580Evaluation of retinal nerve fiber layer thickness measured by optical coherence tomography in Moroccan patients with multiple sclerosis.J Fr Ophtalmol2015
25955371Locked in syndrome revealing an antiphospholipid syndrome.Tunis Med2015
24482476Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders.Science2014
25216553Multiple sclerosis: clinical characteristics and disability progression in Moroccan children.J Neurol Sci2014
24602214Profile of idiopathic parkinson's disease in Moroccan patients.Int Arch Med2014
24321218A clinical study of non-parkinsonian tremor in Moroccan patients.Rev Neurol (Paris)2014
24319291KIF1C mutations in two families with hereditary spastic paraparesis and cerebellar dysfunction.J Med Genet2014
22763206Profile of multiple system atrophy in Moroccan patients attending a movement disorders outpatient clinic in Rabat university hospital.Rev Neurol (Paris)2013
23849771Genetic factors and multiple sclerosis in the Moroccan population: a role for HLA class II.Pathol Biol (Paris)2013
23415906Neurosyphilis revealed by trochlear nerve (IV) palsy.Rev Neurol (Paris)2013
23180398CLN6 p.I154del mutation causing late infantile neuronal ceroid lipofuscinosis in a large consanguineous Moroccan family.Indian J Pediatr2013
23083771[Atypical metastatic sites for adenocarcinoma of the lung].J Fr Ophtalmol2013
22766327Cryptococcosis in an immunocompetent pregnant woman.Rev Neurol (Paris)2013
21665238[Multiple sclerosis associated with antiphospholipid syndrome: diagnostic and therapeutic difficulties].Rev Neurol (Paris)2012
23176821Alteration of fatty-acid-metabolizing enzymes affects mitochondrial form and function in hereditary spastic paraplegia.Am J Hum Genet2012
22703613Parkinsonism as first manifestation of lupus.Rev Neurol (Paris)2012
22436252An autosomal recessive leucoencephalopathy with ischemic stroke, dysmorphic syndrome and retinitis pigmentosa maps to chromosome 17q24.2-25.3.BMC Med Genet2012
22673751[Invasive aspergillosis in a pediatric hematology-oncology ward].Med Mal Infect2012
22560010[Quality of life and multiple sclerosis: Arabic language translation and transcultural adaptation of "MSQOL-54"].Rev Neurol (Paris)2012
22136880Neurological manifestations of Behçet's disease: evaluation of 40 patients treated by cyclophosphamide.Rev Neurol (Paris)2012
20561657[Stroke revealing granulomatosis].Rev Neurol (Paris)2011
20934735[Neuromarketing: When marketing meet neurosciences].Rev Neurol (Paris)2011
19497602[Pachymeningitis associated with probable Horton's disease: a case report].Rev Neurol (Paris)2010
21252451Prevalence of human papillomavirus genotype among Moroccan women during a local screening program.J Infect Dev Ctries2010
19836814[Cerebral venous thrombosis and acute polyradiculoneuritis revealing systemic lupus erythematosus].Rev Neurol (Paris)2010
18758830A locus for bilateral occipital polymicrogyria maps to chromosome 6q16-q22.Neurogenetics2009
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Collaborators

Ahmed Bouhouche
Medical School and Pharmacy, University Mohammed V in Rabat
Co-authored papers 28
Alexis Brice
Sorbonne University, Paris Brain Institute - ICM, Inserm, CNRS
Co-authored papers 25
Naima Bouslam
Specialties Hospital
Co-authored papers 25
Giovanni Stevanin
Sorbonne University, Paris Brain Institute - ICM, Inserm, CNRS
Co-authored papers 21
Alexandra Durr
Sorbonne University, Paris Brain Institute - ICM, Inserm, CNRS
Co-authored papers 20
Sylvain Hanein
Institute of Genetic Diseases, INSERM UMR1163, Imagine and Paris Descartes University
Co-authored papers 4
Sylvie Forlani
ICM DNA and Cell Bank CNRS UMR7225, INSERM U1127, Sorbonne University
Co-authored papers 2
Laure Raymond
Sorbonne Universite, Institut du Cerveau-Paris Brain Institute-ICM, Inserm, CNRS
Co-authored papers 2
Maha S Zaki
Human Genetics and Genome Research Institute, National Research Centre
Co-authored papers 2
Guy A Rouleau
McGill University, Canada Montreal Neurological Institute and Hospital
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University of California
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Ahmet Okay Caglayan
Yale School of Medicine
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Emily G Spencer
Scripps Research Translational Institute
Co-authored papers 1
Ghada M H Abdel-Salam
Human Genetics and Genome Research Institute, National Research Centre
Co-authored papers 1
Jean Weissenbach
Institut Francois Jacob, CNRS, Universite Paris-Saclay
Co-authored papers 1
Asl??han Tolun
Istanbul Technical University
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Stacey Gabriel
Broad Institute of MIT and Harvard
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Bertrand Fontaine
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Massimo Mascaro
Howard Hughes Medical Institute, University of California
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Jumana Y Al-Aama
King AbdulAziz University
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Mostafa Abdellateef
Center for Brain Development, University of California
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Laila Selim
Cairo University
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Release 1.2