Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Journal of Molecular Neuroscience : MN|June 25, 2011
Prothrombin G20210A and factor V Leiden polymorphisms in strokeThierry Paluku They-They, Omar Battas, Ilham Slassi, et al.
BMC Neurology|November 27, 2015
A novel mutation in the ABCD1 gene of a Moroccan patient with X-linked adrenoleukodystrophy: case reportAdnane Karkar, Abdelhamid Barakat, Amina Bakhchane, et al.
Multiple Sclerosis and Related Disorders|February 18, 2019
Clinical course of neuromyelitis optica spectrum disorder in a moroccan cohortAnas Bennis, Hicham El Otmani, Nada Benkirane, et al.
Journal of Molecular Neuroscience : MN|July 16, 2014
A proteomic approach for the involvement of the GAPDH in Alzheimer disease in the blood of Moroccan FAD casesNadia El Kadmiri, Raquel Cuardos, Bouchra El Moutawakil, et al.
Meta Gene|January 22, 2015
G894T endothelial nitric oxide synthase polymorphism and ischemic stroke in MoroccoBrehima Diakite, Khalil Hamzi, Ilham Slassi, et al.
Presse Medicale (Paris, France : 1983)|January 19, 2008
[Cauda equina syndrome leading to diagnosis of malignant non-Hodgkin lymphoma of the spine]Mohammed Abdoh Rafai, Fatima Zohra Boulaajaj, Bouchra El Moutawakkil, et al.
Journal of Molecular Neuroscience : MN|March 15, 2014
Novel mutations in the amyloid precursor protein gene within Moroccan patients with Alzheimer's diseaseNadia El Kadmiri, Nabil Zaid, Ahmed Hachem, et al.
Pediatric Neurology|August 31, 2023
Deep Brain Stimulation for Dystonia: Experience of a Moroccan University HospitalHicham El Otmani, Bouchra El Moutawakil, Mohamed Daghi, et al.
Joint Bone Spine|February 17, 2009
Neurological manifestations revealing primitive Gougerot-Sjogren syndrome: 9 casesMohammed Abdoh Rafai, Fatima Zohra Boulaajaj, Fettouma Moutawakil, et al.
Pageof 3