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L Andreu

Showing results (281-290 of 313) with videos related to

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Annals of Neurology|November 15, 2001
Molecular heterogeneity of myophosphorylase deficiency (McArdle's disease): a genotype-phenotype correlation studyM A Martín, J C Rubio, J Buchbinder, et al.
Antimicrobial Agents and Chemotherapy|July 5, 2017
Influence of Mitochondrial Genetics on the Mitochondrial Toxicity of Linezolid in Blood Cells and Skin Nerve FibersG Garrabou, À Soriano, T Pinós, et al.
The Science of the Total Environment|December 23, 2021
The unknown third - Hydrogen isotopes in tree-ring cellulose across EuropeV Vitali, E Martínez-Sancho, K Treydte, et al.
Rheumatology (Oxford, England)|December 25, 2009
Prediction of functional impairment and remission in rheumatoid arthritis patients by biochemical variables and genetic polymorphismsAlejandro Balsa, Jokin Del Amo, Francisco Blanco, et al.
American Journal of Respiratory Cell and Molecular Biology|February 27, 2023
Biomarkers of Fibrosis in Patients with COVID-19 One Year After Hospital Discharge: A Prospective Cohort StudyAlba Mulet, Julia Tarrasó, Enrique Rodríguez-Borja, et al.
Mitochondrion|March 16, 2010
Marked mitochondrial DNA depletion associated with a novel SUCLG1 gene mutation resulting in lethal neonatal acidosis, multi-organ failure, and interrupted aortic archHenry Rivera, Begoña Merinero, Mercedes Martinez-Pardo, et al.
Scandinavian Journal of Rheumatology|November 3, 2011
The C677T polymorphism in the MTHFR gene is associated with the toxicity of methotrexate in a Spanish rheumatoid arthritis populationR Cáliz, J del Amo, A Balsa, et al.
BMC Medicine|January 8, 2023
Recommendations for robust and reproducible preclinical research in personalised medicineVibeke Fosse, Emanuela Oldoni, Florence Bietrix, et al.
Orphanet Journal of Rare Diseases|October 15, 2020
Creation and implementation of a European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC registry)Tomàs Pinós, Antoni L Andreu, Claudio Bruno, et al.
The Journal of Physiology|January 10, 2018
Muscle molecular adaptations to endurance exercise training are conditioned by glycogen availability: a proteomics-based analysis in the McArdle mouse modelCarmen Fiuza-Luces, Alejandro Santos-Lozano, Francisco Llavero, et al.
Pageof 32

Showing results (281-290 of 313) with videos related to

Sort By:
Pageof 32
Annals of Neurology|November 15, 2001
Molecular heterogeneity of myophosphorylase deficiency (McArdle's disease): a genotype-phenotype correlation studyM A Martín, J C Rubio, J Buchbinder, et al.
Antimicrobial Agents and Chemotherapy|July 5, 2017
Influence of Mitochondrial Genetics on the Mitochondrial Toxicity of Linezolid in Blood Cells and Skin Nerve FibersG Garrabou, À Soriano, T Pinós, et al.
The Science of the Total Environment|December 23, 2021
The unknown third - Hydrogen isotopes in tree-ring cellulose across EuropeV Vitali, E Martínez-Sancho, K Treydte, et al.
Rheumatology (Oxford, England)|December 25, 2009
Prediction of functional impairment and remission in rheumatoid arthritis patients by biochemical variables and genetic polymorphismsAlejandro Balsa, Jokin Del Amo, Francisco Blanco, et al.
American Journal of Respiratory Cell and Molecular Biology|February 27, 2023
Biomarkers of Fibrosis in Patients with COVID-19 One Year After Hospital Discharge: A Prospective Cohort StudyAlba Mulet, Julia Tarrasó, Enrique Rodríguez-Borja, et al.
Mitochondrion|March 16, 2010
Marked mitochondrial DNA depletion associated with a novel SUCLG1 gene mutation resulting in lethal neonatal acidosis, multi-organ failure, and interrupted aortic archHenry Rivera, Begoña Merinero, Mercedes Martinez-Pardo, et al.
Scandinavian Journal of Rheumatology|November 3, 2011
The C677T polymorphism in the MTHFR gene is associated with the toxicity of methotrexate in a Spanish rheumatoid arthritis populationR Cáliz, J del Amo, A Balsa, et al.
BMC Medicine|January 8, 2023
Recommendations for robust and reproducible preclinical research in personalised medicineVibeke Fosse, Emanuela Oldoni, Florence Bietrix, et al.
Orphanet Journal of Rare Diseases|October 15, 2020
Creation and implementation of a European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC registry)Tomàs Pinós, Antoni L Andreu, Claudio Bruno, et al.
The Journal of Physiology|January 10, 2018
Muscle molecular adaptations to endurance exercise training are conditioned by glycogen availability: a proteomics-based analysis in the McArdle mouse modelCarmen Fiuza-Luces, Alejandro Santos-Lozano, Francisco Llavero, et al.
Pageof 32