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Articles, 2 records found
Articles 2 records found  
1.
15 p, 9.5 MB Low aerobic capacity in McArdle disease : A role for mitochondrial network impairment? / Villarreal-Salazar, M. (Hospital Universitari Vall d'Hebron) ; Santalla, A. (Universidad Pablo de Olavide) ; Real-Martinez, Alberto (Hospital Universitari Vall d'Hebron) ; Nogales, Gisela (Institut Germans Trias i Pujol. Hospital Universitari Germans Trias i Pujol) ; Valenzuela, P.L. (Hospital Universitario 12 de Octubre (Madrid)) ; Fiuza-Luces, C. (Hospital Universitario 12 de Octubre (Madrid)) ; Andreu, A. L. (European Infrastructure for Translational Medicine) ; Rodríguez-Aguilera, J.C. (Universidad Pablo de Olavide) ; Martín, M.A. (Hospital Universitario 12 de Octubre (Madrid)) ; Arenas, Joaquín (Hospital Universitario 12 de Octubre (Madrid)) ; Vissing, J. (University of Copenhagen) ; Lucia, A. (European University) ; Krag, T.O. (University of Copenhagen) ; Pinós Figueras, Tomàs (Hospital Universitari Vall d'Hebron) ; Universitat Autònoma de Barcelona
McArdle disease is caused by myophosphorylase deficiency and results in complete inability for muscle glycogen breakdown. A hallmark of this condition is muscle oxidation impairment (e. g. , low peak oxygen uptake (VO)), a phenomenon traditionally attributed to reduced glycolytic flux and Krebs cycle anaplerosis. [...]
2022 - 10.1016/j.molmet.2022.101648
Molecular metabolism, Vol. 66 (november 2022)  
Detailed record - Creative Commons
2.
8 p, 618.0 KB A Transcriptomic Approach to Search for Novel Phenotypic Regulators in McArdle Disease / Nogales, Gisela (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Consuegra-García, Inés (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Rubio, Juan C. (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Arenas, Joaquín (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Cuadros, Marc (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Cámara, Yolanda (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Torres-Torronteras, Javier (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Fiuza-Luces, Carmen (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Lucia, Alejandro (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Martín, Miguel A. (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Garcia-Arumi, Elena (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Andreu Périz, Antoni Lluís (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Universitat Autònoma de Barcelona
McArdle disease is caused by lack of glycogen phosphorylase (GP) activity in skeletal muscle. Patients experience exercise intolerance, presenting as early fatigue and contractures. In this study, we investigated the effects produced by a lack of GP on several genes and proteins of skeletal muscle in McArdle patients. [...]
2012 - 10.1371/journal.pone.0031718
PloS one, Vol. 7 (february 2012)  
Detailed record - Creative Commons

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1 Fiuza-Luces, Carmen
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