Publications by authors named "Ali Benomar"

39Publications

Gene Panel Sequencing Identifies Novel Pathogenic Mutations in Moroccan Patients with Familial Parkinson Disease.

J Mol Neurosci 2020 Jun 16. Epub 2020 Jun 16.

Neurology and Neurogenetics, Faculty of Medicine and Pharmacy, Genomics Center of Human Pathologies, University Mohammed V, Rabat, Morocco.

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http://dx.doi.org/10.1007/s12031-020-01635-3DOI Listing
June 2020

[Current antiplatelet agents, new inhibitors and therapeutic targets].

Med Sci (Paris) 2020 Apr 1;36(4):348-357. Epub 2020 May 1.

Research Center of Abulcasis University of Health Sciences, Rabat, Maroc - Faculty of Sciences, Department of Biology, Mohammed V University, Rabat, Maroc.

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http://dx.doi.org/10.1051/medsci/2020061DOI Listing
April 2020

A case of bilateral thalamic infarct complicating tuberculous meningoencephalitis.

Pan Afr Med J 2019 6;33. Epub 2019 May 6.

Department of Neurology and Neurogenetics, Hôpital des Spécialités ONO, CHU Rabat-Salé, Morocco.

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http://dx.doi.org/10.11604/pamj.2019.33.2.13327DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6607461PMC
July 2019

Genetic Analysis of Undiagnosed Juvenile GM1-Gangliosidosis by Microarray and Exome Sequencing.

Case Rep Genet 2018 15;2018:8635698. Epub 2018 Nov 15.

Genetics Center of the Cheikh Zayed Foundation, Abulcasis International University of Health Sciences, Rabat, Morocco.

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http://dx.doi.org/10.1155/2018/8635698DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6276426PMC
November 2018

Non-Motor Symptoms of Parkinson's Disease and Their Impact on Quality of Life in a Cohort of Moroccan Patients.

Front Neurol 2018 4;9:170. Epub 2018 Apr 4.

Research Team in Neurology and Neurogenetics, Faculty of Medicine and Pharmacy, Genomics Center of Human Pathologies, University Mohammed V, Rabat, Morocco.

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http://dx.doi.org/10.3389/fneur.2018.00170DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5893866PMC
April 2018

Mutation Analysis of Consanguineous Moroccan Patients with Parkinson's Disease Combining Microarray and Gene Panel.

Front Neurol 2017 31;8:567. Epub 2017 Oct 31.

Sorbonne Universités, UPMC Université Paris 6 UMR_S 1127, INSERM U 1127, CNRS UMR 7225, Institut du Cerveau et de la Moelle épinière, ICM, Paris, France.

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http://dx.doi.org/10.3389/fneur.2017.00567DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5674924PMC
October 2017

Evidence for prehistoric origins of the G2019S mutation in the North African Berber population.

PLoS One 2017 19;12(7):e0181335. Epub 2017 Jul 19.

Research Team in Neurology and Neurogenetics, Genomics Center of Human Pathologies, Medical School and Pharmacy, Mohammed V University, Rabat, Morocco.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0181335PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5517005PMC
September 2017

G2019S Mutation: Prevalence and Clinical Features in Moroccans with Parkinson's Disease.

Parkinsons Dis 2017 30;2017:2412486. Epub 2017 Mar 30.

Research Team in Neurology and Neurogenetics, Medical School and Pharmacy, Mohammed V University, Rabat, Morocco.

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http://dx.doi.org/10.1155/2017/2412486DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5390546PMC
March 2017

A Novel Homozygous p.L539F Mutation Identified in PINK1 Gene in a Moroccan Patient with Parkinsonism.

Biomed Res Int 2016 20;2016:3460234. Epub 2016 Jun 20.

Research Team on Neurodegenerative Diseases, Medical School and Pharmacy, Mohammed V University, 10100 Rabat, Morocco; Department of Neurology and Neurogenetics, Specialties Hospital, CHU Ibn Sina, 10100 Rabat, Morocco.

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http://dx.doi.org/10.1155/2016/3460234DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4931068PMC
March 2017

Clinical and genetic data of Huntington disease in Moroccan patients.

Afr Health Sci 2015 Dec;15(4):1232-8

Equipe de Recherche sur les Maladies Neurodégénératives, Faculté de Médecine et de Pharmacie, Université Mohammed V de Rabat, Morocco; Service de Neurologie et de Neurogénétique, Hôpital des Spécialités de Rabat, Morocco.

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http://dx.doi.org/10.4314/ahs.v15i4.23DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4765413PMC
December 2015

[Pathological and clinical correlations in renal AA amyloidosis: A Moroccan series of 30 cases].

Nephrol Ther 2015 Dec 23;11(7):543-50. Epub 2015 Oct 23.

Laboratoire d'anatomie cytologie pathologiques, faculté de médecine et de pharmacie, université Mohamed V, hôpital d'enfants, Rabat, Maroc.

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http://dx.doi.org/10.1016/j.nephro.2015.06.007DOI Listing
December 2015

Measles in Morocco: epidemiological profile and impact of vaccination strategy.

Adv Ther 2015 Feb 3;32(2):172-83. Epub 2015 Mar 3.

Faculty of Medicine, Abulcasis University, Rabat, Morocco,

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http://dx.doi.org/10.1007/s12325-015-0188-2DOI Listing
February 2015

Multiple sclerosis: clinical characteristics and disability progression in Moroccan children.

J Neurol Sci 2014 Nov 13;346(1-2):128-32. Epub 2014 Aug 13.

Department of Neurology B and Neurogenetics, Hôpital des Spécialités Rabat, Faculté de Médecine et de Pharmacie Rabat, Mohammed V University Souissi, Rabat, Morocco. Electronic address:

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http://dx.doi.org/10.1016/j.jns.2014.08.008DOI Listing
November 2014

Profile of idiopathic parkinson's disease in Moroccan patients.

Int Arch Med 2014 Mar 6;7(1):10. Epub 2014 Mar 6.

Department of Neurology B and Neurogenetics, Hôpital des Spécialités O.N.O, 6444 Rabat, Morocco.

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http://dx.doi.org/10.1186/1755-7682-7-10DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3946767PMC
March 2014

KIF1C mutations in two families with hereditary spastic paraparesis and cerebellar dysfunction.

J Med Genet 2014 Feb 6;51(2):137-42. Epub 2013 Dec 6.

Department of Pediatrics, Neuropediatric Unit, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.

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http://dx.doi.org/10.1136/jmedgenet-2013-102012DOI Listing
February 2014

CLN6 p.I154del mutation causing late infantile neuronal ceroid lipofuscinosis in a large consanguineous Moroccan family.

Indian J Pediatr 2013 Aug 22;80(8):694-6. Epub 2012 Nov 22.

Service de Neurologie et de Neurogénétique, Hôpital des Spécialités, BP, 6402 Al Irfane, Rabat, Morocco.

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http://dx.doi.org/10.1007/s12098-012-0889-3DOI Listing
August 2013

Prevalence of human papillomavirus genotype among Moroccan women during a local screening program.

J Infect Dev Ctries 2010 Nov 24;4(11):732-9. Epub 2010 Nov 24.

Maternité Souissi, Centre Hospitalier Universitaire Ibn Sina. Rabat, Morocco.

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http://dx.doi.org/10.3855/jidc.781DOI Listing
November 2010

A novel GDAP1 mutation P78L responsible for CMT4A disease in three Moroccan families.

Can J Neurol Sci 2007 Nov;34(4):421-6

Service de Neurologie et de Neurogénétique, Hôpital des Spécialités, BP 6402, Al Irfane Rabat, Morocco.

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http://dx.doi.org/10.1017/s0317167100007290DOI Listing
November 2007

Autosomal recessive mutilating sensory neuropathy with spastic paraplegia maps to chromosome 5p15.31-14.1.

Eur J Hum Genet 2006 Feb;14(2):249-52

Service de Neurologie et de Neurogénétique, Hôpital des Spécialités, Rabat, Morocco.

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http://dx.doi.org/10.1038/sj.ejhg.5201537DOI Listing
February 2006

Vitamin E deficiency ataxia with (744 del A) mutation on alpha-TTP gene: genetic and clinical peculiarities in Moroccan patients.

Eur J Med Genet 2005 Jan-Mar;48(1):21-8. Epub 2005 Feb 19.

Molecular Genetics Laboratory, Faculty of Sciences, The Department of Neurology, University of Fez Sidi Med Benabdellah, Hospital of Rabat, Morocco.

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http://dx.doi.org/10.1016/j.ejmg.2005.01.014DOI Listing
August 2005

Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28).

Ann Neurol 2005 Apr;57(4):567-71

INSERM U679 (former U289), Federative Institute for Neuroscience Research (IFR70), Salpetriere Hospital, Paris, France.

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http://dx.doi.org/10.1002/ana.20416DOI Listing
April 2005