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Neuromuscular Disorders : NMD|August 22, 2021
Whole exome sequencing reveals a homozygous C1QBP deletion as the cause of progressive external ophthalmoplegia and multiple mtDNA deletionsLe Guo, Periyasamy Govindaraj, Mariëlle Kievit, et al.Journal of Neurogenetics|May 2, 2022
Novel insights into the genetic profile of hereditary spastic paraplegia in IndiaSundarapandian Narendiran, Monojit Debnath, Sumanth Shivaram, et al.Neurogenetics|April 15, 2010
Novel SPG11 mutations in Asian kindreds and disruption of spatacsin function in the zebrafishLaura Southgate, Dimitra Dafou, Jacqueline Hoyle, et al.Mitochondrion|September 6, 2015
Magnetic resonance imaging correlates of genetically characterized patients with mitochondrial disorders: A study from south IndiaParayil Sankaran Bindu, Hanumanthapura Arvinda, Arun B Taly, et al.Plos One|May 20, 2016
Genetic Analysis of PLA2G6 in 22 Indian Families with Infantile Neuroaxonal Dystrophy, Atypical Late-Onset Neuroaxonal Dystrophy and Dystonia Parkinsonism ComplexSaketh Kapoor, Mohd Hussain Shah, Nivedita Singh, et al.Mitochondrion|January 15, 2016
Peripheral neuropathy in genetically characterized patients with mitochondrial disorders: A study from south IndiaParayil Sankaran Bindu, Chikanna Govindaraju, Kothari Sonam, et al.Epilepsy Research|March 19, 2021
Role of pulse methylprednisolone in epileptic encephalopathy: A retrospective observational analysisAparajita Chatterjee, Ravindranadh Chowdary Mundlamuri, Raghavendra Kenchaiah, et al.Journal of Neurology|January 23, 2021
Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndromeSanjiban Chakrabarty, Periyasamy Govindaraj, Bindu Parayil Sankaran, et al.Sleep Medicine|February 18, 2021
Sleep profile and Polysomnography in patients with drug-resistant temporal lobe epilepsy (TLE) due to hippocampal sclerosis (HS) and the effect of epilepsy surgery on sleep-a prospective cohort studySai Deepak Yaranagula, Ajay Asranna, Madhu Nagappa, et al.Clinical Neurology and Neurosurgery|December 23, 2017
Outcome of epilepsy in patients with mitochondrial disorders: Phenotype genotype and magnetic resonance imaging correlationsParayil Sankaran Bindu, Kothari Sonam, Periyasamy Govindaraj, et al.Pageof 29