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Gene|June 19, 2015
Homozygous MAPT R406W mutation causing FTDP phenotype: A unique instance of a unique mutationMahdiyeh Behnam, Fatemeh Ghorbani, Jin-Hong Shin, et al.
Current Journal of Neurology|November 27, 2023
Guillain-Barre syndrome in patients with coronavirus disease-2019: Report of six cases and review of literatureAli Asghar Okhovat, Behnaz Ansari, Helia Hemasian, et al.
Annals of Clinical and Translational Neurology|September 28, 2019
Motor neuron diseases caused by a novel VRK1 variant - A genotype/phenotype studyMaryam Sedghi, Ali-Reza Moslemi, Montse Olive, et al.
Clinical Neuroradiology|December 15, 2022
Clinical and Neuroimaging Characteristics of Ischemic Stroke in Rhino-Orbito-Cerebral Mucormycosis Associated with COVID-19Mohammad Amin Najafi, Alireza Zandifar, Neda Ramezani, et al.
Movement Disorders Clinical Practice|January 26, 2023
Childhood-Onset Choreo-Dystonia Due to a Recurrent Novel Homozygous Nonsense HPCA Variant: Case Series and Literature ReviewFrancesca Magrinelli, Kailash P Bhatia, Mehran Beiraghi Toosi, et al.
Basic and Clinical Neuroscience|February 17, 2022
Guillain-Barre Syndrome and COVID-19 Vaccine: A Report of Nine PatientsNarges Karimi, Reza Boostani, Farzad Fatehi, et al.
Muscle & Nerve|January 19, 2020
Quantitative muscle MRI study of patients with sporadic inclusion body myositisBehnaz Ansari, Emmanuelle Salort-Campana, Augustin Ogier, et al.
Frontiers in Neurology|October 8, 2021
Recommendations for Infantile-Onset and Late-Onset Pompe Disease: An Iranian ConsensusFarzad Fatehi, Mahmoud Reza Ashrafi, Marzieh Babaee, et al.
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