Publications by authors named "Bouchra Ouled Amar Bencheikh"

18Publications

Variants in the Niemann-Pick type C gene NPC1 are not associated with Parkinson's disease.

Neurobiol Aging 2020 09 8;93:143.e1-143.e4. Epub 2020 Apr 8.

Montreal Neurological Institute, McGill University, Montréal, Quebec, Canada; Department of Neurology and neurosurgery, McGill University, Montréal, Quebec, Canada; Department of Human Genetics, McGill University, Montréal, Quebec, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.neurobiolaging.2020.03.021DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7302975PMC
September 2020

Can the microbiota predict response to systemic cancer therapy, surgical outcomes, and survival? The answer is in the gut.

Expert Rev Clin Pharmacol 2020 Apr 24;13(4):403-421. Epub 2020 May 24.

Faculty of Medicine and Pharmacy, Mohamed Ist University , Oujda, Morocco.

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http://dx.doi.org/10.1080/17512433.2020.1758063DOI Listing
April 2020

Targeted knockout of GABA-A receptor gamma 2 subunit provokes transient light-induced reflex seizures in zebrafish larvae.

Dis Model Mech 2019 11 11;12(11). Epub 2019 Nov 11.

Research Center of the University of Montreal Hospital Center (CRCHUM), Department of Neurosciences, Université de Montréal, Montréal, QC H2X 0A9, Canada

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http://dx.doi.org/10.1242/dmm.040782DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6899022PMC
November 2019

Common and rare GCH1 variants are associated with Parkinson's disease.

Neurobiol Aging 2019 01 15;73:231.e1-231.e6. Epub 2018 Sep 15.

Department of Human Genetics, McGill University, Montréal, Quebec, Canada; Montreal Neurological Institute, McGill University, Montréal, Quebec, Canada; Department of Neurology and Neurosurgery, McGill University, Montréal, Quebec, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.neurobiolaging.2018.09.008DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6251729PMC
January 2019

Sequencing of the GBA coactivator, Saposin C, in Parkinson disease.

Neurobiol Aging 2018 12 2;72:187.e1-187.e3. Epub 2018 Jul 2.

Montreal Neurological Institute, McGill University, Montréal, QC, Canada; Department of Neurology and Neurosurgery, McGill University, Montréal, QC, Canada; McGill Parkinson Program and Neurodegenerative Diseases Group, Montreal Neurological Institute, McGill University, Montréal, QC, Canada; Department of Human Genetics, McGill University, Montréal, QC, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.neurobiolaging.2018.06.034DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6215722PMC
December 2018

LRRK2 protective haplotype and full sequencing study in REM sleep behavior disorder.

Parkinsonism Relat Disord 2018 07 21;52:98-101. Epub 2018 Mar 21.

Montreal Neurological Institute, McGill University, Montréal, QC, H3A 0G4, Canada; Department of Neurology and Neurosurgery, McGill University, Montréal, QC, H3A 0G4, Canada, Canada; Department of Human Genetics, McGill University, H3A 0G4, Montréal, QC, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.parkreldis.2018.03.019DOI Listing
July 2018

A novel nonsense mutation in SCN9A in a Moroccan child with congenital insensitivity to pain.

Pediatr Neurol 2014 Nov 12;51(5):741-4. Epub 2014 Jul 12.

Neurology and Neurosurgery Department, McGill University, Montréal, Quebec, Canada; Montreal Neurological Institute and Hospital, McGill University, Montréal, Quebec, Canada.

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http://dx.doi.org/10.1016/j.pediatrneurol.2014.06.009DOI Listing
November 2014

Role of the phosphoinositide phosphatase FIG4 gene in familial epilepsy with polymicrogyria.

Neurology 2014 Mar 5;82(12):1068-75. Epub 2014 Mar 5.

From INSERM (S.B., B.D., B.O.A.B., P.C., J.R., E.N., K.H.E.H., E.L.), U1127; Sorbonne Universités, UPMC Univ Paris 06 (S.B., B.D., B.O.A.B., P.C., J.R., E.N., K.H.E.H., E.L.), UM 75; CNRS (S.B., B.D., B.O.A.B., P.C., J.R., E.N., K.H.E.H., E.L.), UMR 7225, ICM, Paris, ICM, (S.B., B.D., B.O.A.B., P.C., J.R., E.N., K.H.E.H., E.L.) Paris, F-75013 Paris, France; Department of Human Genetics (G.M.L., P.A.L., C.J.F., M.H.M.), University of Michigan, Ann Arbor; Service de Neurophysiologie Clinique (B.O.A.B.), Hôpital des Spécialités, Centre Hospitalier Ibn Sina Rabat, Morocco; Genetics and Pathophysiology of Neurodevelopmental and Neuromuscular Diseases (K.P.), Cochin Institute, Paris; GenoScreen (C.H., S.F.), Lille, France; Neuroscience Department (R.G.), Children's Hospital A. Meyer, University of Florence and IRCCS Stella Maris, Pisa, Italy; Laboratoire de Neurogénétique (K.H.E.H.), Ecole Pratique des Hautes Etudes, Paris; and Département de Génétique et de Cytogénétique (E.L.), AP-HP Groupe hospitalier Pitié-Salpêtrière, Paris, France.

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http://dx.doi.org/10.1212/WNL.0000000000000241DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3962989PMC
March 2014