Showing results (251-260 of 290) with videos related to
Sort By:
Pageof 29
Spinal Cord|February 20, 1999
Heterotopic ossification in non-traumatic myelopathiesA B Taly, K P Nair, M V Kumar, et al.Clinical Neuropathology|April 25, 2000
Inclusion body myositis (IBM)N Gayathri, Anisya-Vasanth, M Veerendra Kumar, et al.Neurology India|November 10, 2022
Insights from Magnetic Evoked Field Analysis in Patients with Wilson's DiseaseR Aruna, N Mariyappa, S Sinha, et al.Epilepsy Research|June 20, 2015
Management of generalised convulsive status epilepticus (SE): A prospective randomised controlled study of combined treatment with intravenous lorazepam with either phenytoin, sodium valproate or levetiracetam--Pilot studyR C Mundlamuri, S Sinha, D K Subbakrishna, et al.Neuropediatrics|May 15, 2015
Clinical and Neuroimaging Features in Two Children with Mutations in the Mitochondrial ND5 GeneKothari Sonam, P S Bindu, Arun B Taly, et al.Journal of Molecular Neuroscience : MN|January 20, 2021
Clinico-pathological and Molecular Spectrum of Mitochondrial Polymerase γ Mutations in a Cohort from IndiaSekar Deepha, Periyasamy Govindaraj, Bindu Parayil Sankaran, et al.Neurology India|November 6, 2023
Characterisation of Patients with SH3TC2 Associated Neuropathy in an Indian CohortMadhu Nagappa, Shivani Sharma, Periyasamy Govindaraj, et al.Muscle & Nerve|September 17, 2020
Ganglioside complex antibodies in an Indian cohort of Guillain-Barré syndromeRahul Wahatule, Debprasad Dutta, Monojit Debnath, et al.Plos One|May 7, 2019
Genetic analysis of ATP7B in 102 south Indian families with Wilson diseaseNivedita Singh, Pradeep Kallollimath, Mohd Hussain Shah, et al.Brain & Development|November 23, 2013
Clinical and magnetic resonance imaging findings in patients with Leigh syndrome and SURF1 mutationsKothari Sonam, Nahid Akthar Khan, Parayil Sankaran Bindu, et al.Pageof 29