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Muscles (Basel, Switzerland)|August 4, 2025
Clinical Advances in Neuromuscular Diseases: Neurometabolic DisordersCorrado Angelini, Daniela Tavian
Critical Reviews in Biochemistry and Molecular Biology|April 7, 2021
ETF dehydrogenase advances in molecular genetics and impact on treatmentSara Missaglia, Daniela Tavian, Corrado Angelini
European Journal of Translational Myology|June 17, 2022
Neutral lipid storage disease with myopathy: A 10-year follow-up case reportSara Missaglia, Daniela Tavian, Corrado Angelini
JIMD Reports|May 1, 2017
Heterogeneous Phenotypes in Lipid Storage Myopathy Due to ETFDH Gene MutationsCorrado Angelini, Daniela Tavian, Sara Missaglia
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 15, 2011
Selective underexpression of Kv3.2 and Kv3.4 channels in the cortex of rats exposed to ethanol during early postnatal lifeDaniela Tavian, Andrea De Giorgio, Alberto Granato
Lipids in Health and Disease|November 15, 2018
Characterization of two ETFDH mutations in a novel case of riboflavin-responsive multiple acyl-CoA dehydrogenase deficiencySara Missaglia, Daniela Tavian, Laura Moro, et al.
BMC Medical Genetics|May 31, 2018
Clinical and genetic characterization of a Chanarin Dorfman Syndrome patient born to diseased parentsMurat Durdu, Sara Missaglia, Laura Moro, et al.
Therapeutic Advances in Neurological Disorders|May 2, 2019
Metabolic lipid muscle disorders: biomarkers and treatmentCorrado Angelini, Elena Pennisi, Sara Missaglia, et al.
Journal of Experimental & Clinical Cancer Research : CR|March 12, 2021
ROS-dependent HIF1α activation under forced lipid catabolism entails glycolysis and mitophagy as mediators of higher proliferation rate in cervical cancer cellsSerena Castelli, Fabio Ciccarone, Daniela Tavian, et al.
Cells|February 24, 2019
Neutral Lipid Storage Diseases as Cellular Model to Study Lipid Droplet FunctionSara Missaglia, Rosalind A Coleman, Alvaro Mordente, et al.
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