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DiMauro

Showing results (451-460 of 942) with videos related to

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Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy|June 7, 2008
Raman, IR, UV-vis and EPR characterization of two copper dioxolene complexes derived from L-dopa and dopamineWagner J Barreto, Sônia R G Barreto, Rômulo A Ando, et al.
Neurology|February 1, 1993
Phosphoglycerate kinase deficiency: biochemical and molecular genetic studies in a new myopathic variant (PGK Alberta)P Tonin, S Shanske, A F Miranda, et al.
Cardio-Oncology (London, England)|April 27, 2023
Cardiac and noncardiac biomarkers in patients undergoing anthracycline chemotherapy - a prospective analysisMatthew Dean, Min Jung Kim, Sharon Dimauro, et al.
Deutsche Medizinische Wochenschrift (1946)|July 8, 1983
[Muscular carnitine-palmityl-transferase deficiency]K W Rumpf, H Kaiser, H H Goebel, et al.
Physical Review Letters|May 16, 2020
Universal High-Energy Photoelectron Emission from Nanoclusters Beyond the Atomic LimitZhou Wang, Abraham Camacho Garibay, Hyunwook Park, et al.
Neurology|June 9, 2004
A novel mitochondrial tRNAPhe mutation causes MERRF syndromeM Mancuso, M Filosto, V K Mootha, et al.
Free Radical Biology & Medicine|October 14, 2015
SFRR-E Young Investigator AwardeeαB-crystallin modulation after acute exercise in skeletal muscle: the role of oxidative stress and fiber compositionElisa Grazioli, Ivan Dimauro, Neri Mercatelli, et al.
International Journal of Environmental Research and Public Health|October 13, 2021
Effect of Tadalafil Administration on Redox Homeostasis and Polyamine Levels in Healthy Men with High Level of Physical ActivityGuglielmo Duranti, Roberta Ceci, Luigi Di Luigi, et al.
Neuromuscular Disorders : NMD|March 1, 1997
Sudden infant death syndrome (SIDS) in a family with myophosphorylase deficiencyM el-Schahawi, C Bruno, S Tsujino, et al.
Journal of Inherited Metabolic Disease|December 31, 1998
Comparative biochemical studies of ATPases in cells from patients with the T8993G or T8993C mitochondrial DNA mutationsM E Vázquez-Memije, S Shanske, F M Santorelli, et al.
Pageof 95

Showing results (451-460 of 942) with videos related to

Sort By:
Pageof 95
Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy|June 7, 2008
Raman, IR, UV-vis and EPR characterization of two copper dioxolene complexes derived from L-dopa and dopamineWagner J Barreto, Sônia R G Barreto, Rômulo A Ando, et al.
Neurology|February 1, 1993
Phosphoglycerate kinase deficiency: biochemical and molecular genetic studies in a new myopathic variant (PGK Alberta)P Tonin, S Shanske, A F Miranda, et al.
Cardio-Oncology (London, England)|April 27, 2023
Cardiac and noncardiac biomarkers in patients undergoing anthracycline chemotherapy - a prospective analysisMatthew Dean, Min Jung Kim, Sharon Dimauro, et al.
Deutsche Medizinische Wochenschrift (1946)|July 8, 1983
[Muscular carnitine-palmityl-transferase deficiency]K W Rumpf, H Kaiser, H H Goebel, et al.
Physical Review Letters|May 16, 2020
Universal High-Energy Photoelectron Emission from Nanoclusters Beyond the Atomic LimitZhou Wang, Abraham Camacho Garibay, Hyunwook Park, et al.
Neurology|June 9, 2004
A novel mitochondrial tRNAPhe mutation causes MERRF syndromeM Mancuso, M Filosto, V K Mootha, et al.
Free Radical Biology & Medicine|October 14, 2015
SFRR-E Young Investigator AwardeeαB-crystallin modulation after acute exercise in skeletal muscle: the role of oxidative stress and fiber compositionElisa Grazioli, Ivan Dimauro, Neri Mercatelli, et al.
International Journal of Environmental Research and Public Health|October 13, 2021
Effect of Tadalafil Administration on Redox Homeostasis and Polyamine Levels in Healthy Men with High Level of Physical ActivityGuglielmo Duranti, Roberta Ceci, Luigi Di Luigi, et al.
Neuromuscular Disorders : NMD|March 1, 1997
Sudden infant death syndrome (SIDS) in a family with myophosphorylase deficiencyM el-Schahawi, C Bruno, S Tsujino, et al.
Journal of Inherited Metabolic Disease|December 31, 1998
Comparative biochemical studies of ATPases in cells from patients with the T8993G or T8993C mitochondrial DNA mutationsM E Vázquez-Memije, S Shanske, F M Santorelli, et al.
Pageof 95