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Antoni L Andreu

Showing results (71-80 of 77) with videos related to

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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.
Age (Dordrecht, Netherlands)|October 29, 2013
The rs1333049 polymorphism on locus 9p21.3 and extreme longevity in Spanish and Japanese cohortsTomàs Pinós, Noriyuki Fuku, Yolanda Cámara, et al.
BMC Genomics|November 17, 2017
Genotypic and phenotypic features of all Spanish patients with McArdle disease: a 2016 updateAlfredo Santalla, Gisela Nogales-Gadea, Alberto Blázquez Encinar, et al.
Plos One|May 7, 2014
Mitochondrial DAMPs induce endotoxin tolerance in human monocytes: an observation in patients with myocardial infarctionIrene Fernández-Ruiz, Francisco Arnalich, Carolina Cubillos-Zapata, et al.
Orphanet Journal of Rare Diseases|November 25, 2020
Data from the European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC)Renata S Scalco, Alejandro Lucia, Alfredo Santalla, et al.
Orphanet Journal of Rare Diseases|July 24, 2023
Data from the European registry for patients with McArdle disease (EUROMAC): functional status and social participationWalaa Karazi, Renata S Scalco, Mads G Stemmerik, et al.
Pageof 8

Showing results (71-80 of 77) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 77 results.
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.
Age (Dordrecht, Netherlands)|October 29, 2013
The rs1333049 polymorphism on locus 9p21.3 and extreme longevity in Spanish and Japanese cohortsTomàs Pinós, Noriyuki Fuku, Yolanda Cámara, et al.
BMC Genomics|November 17, 2017
Genotypic and phenotypic features of all Spanish patients with McArdle disease: a 2016 updateAlfredo Santalla, Gisela Nogales-Gadea, Alberto Blázquez Encinar, et al.
Plos One|May 7, 2014
Mitochondrial DAMPs induce endotoxin tolerance in human monocytes: an observation in patients with myocardial infarctionIrene Fernández-Ruiz, Francisco Arnalich, Carolina Cubillos-Zapata, et al.
Orphanet Journal of Rare Diseases|November 25, 2020
Data from the European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC)Renata S Scalco, Alejandro Lucia, Alfredo Santalla, et al.
Orphanet Journal of Rare Diseases|July 24, 2023
Data from the European registry for patients with McArdle disease (EUROMAC): functional status and social participationWalaa Karazi, Renata S Scalco, Mads G Stemmerik, et al.
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