Showing results (151-160 of 326) with videos related to
Sort By:
Pageof 33
AJNR. American Journal of Neuroradiology|November 3, 2022
Expanding the Spectrum of Early Neuroradiologic Findings in β Propeller Protein-Associated NeurodegenerationA Papandreou, A K S Soo, R Spaull, et al.Drug and Chemical Toxicology|May 27, 2021
Resveratrol-mediated cardioprotection against myocardial ischemia-reperfusion injury was revoked by statin-induced mitochondrial alterationsRamalingam C Vedarathinam, Yogeshwari Rajkumar, Priya Vetriselvan, et al.JAMA Surgery|January 18, 2013
Partial anterior vs partial posterior fundoplication following transabdominal esophagocardiomyotomy for achalasia of the esophagus: meta-regression of objective postoperative gastroesophageal reflux and dysphagiaAshwin A Kurian, Neil Bhayani, Ahmed Sharata, et al.Molecular Genetics and Metabolism|December 17, 2009
A novel PCFT gene mutation (p.Cys66LeufsX99) causing hereditary folate malabsorptionEsther Meyer, Manju A Kurian, Shanaz Pasha, et al.Molecular Biology Reports|June 2, 2026
MOTS-c preserves mitochondrial subpopulation bioenergetics and genome integrity to attenuate cardiac ischemia reperfusion injurySaranya Sri Santhanam, Srijan Jayaraman, Samyuktha Sharma Rajesh, et al.Naunyn-Schmiedeberg'S Archives of Pharmacology|August 2, 2021
Evaluating the effects of carbon monoxide releasing molecule-2 against myocardial ischemia-reperfusion injury in ovariectomized female ratsArthi Kumar, Sri Rahavi Boovarahan, Priyanka N Prem, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 17, 2004
Neonatal seizures and limb malformations associated with liver-specific complex IV respiratory chain deficiencyM A Kurian, E S O'Mahoney, P Rustin, et al.Journal of Inherited Metabolic Disease|April 7, 2004
Straight-chain acyl-CoA oxidase deficiency presenting with dysmorphia, neurodevelopmental autistic-type regression and a selective pattern of leukodystrophyM A Kurian, S Ryan, G T N Besley, et al.Movement Disorders : Official Journal of the Movement Disorder Society|August 9, 2024
Severe Acute Motor Exacerbations (SAME) across Metabolic, Developmental and Genetic DisordersBlas Couto, Serena Galosi, Dora Steel, et al.Frontiers in Genetics|December 2, 2022
Age-associated global DNA hypermethylation augments the sensitivity of hearts towards ischemia-reperfusion injurySri Rahavi Boovarahan, Nemat Ali, Abdullah F AlAsmari, et al.Pageof 33