CIENCIAS DEL DEPORTE
Departamento
Universitat Autònoma de Barcelona
Barcelona, EspañaPublicaciones en colaboración con investigadores/as de Universitat Autònoma de Barcelona (53)
2024
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Acute ketone supplementation in the absence of muscle glycogen utilization: Insights from McArdle disease
Clinical Nutrition, Vol. 43, Núm. 3, pp. 692-700
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Dose–response effect of pre-exercise carbohydrates under muscle glycogen unavailability: Insights from McArdle disease
Journal of Sport and Health Science
2023
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Data from the European registry for patients with McArdle disease (EUROMAC): functional status and social participation
Orphanet Journal of Rare Diseases, Vol. 18, Núm. 1
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Measuring optimal psychological states: Proposal of two brief versions to measure flow and clutch in athletes
Frontiers in Psychology, Vol. 14
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Mujeres y deporte en España: avances y desafíos hacia la igualdad
Sociología del deporte (Dykinson), pp. 21-42
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Muscle glycogen unavailability and fat oxidation rate during exercise: Insights from McArdle disease
Journal of Physiology, Vol. 601, Núm. 3, pp. 551-566
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Sex Differences in the Association between Risk of Anterior Cruciate Ligament Rupture and COL5A1 Polymorphisms in Elite Footballers
Genes, Vol. 14, Núm. 1
2022
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Identification of Potential Muscle Biomarkers in McArdle Disease: Insights from Muscle Proteome Analysis
International Journal of Molecular Sciences, Vol. 23, Núm. 9
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Long-Term Exercise Intervention in Patients with McArdle Disease: Clinical and Aerobic Fitness Benefits
Medicine and science in sports and exercise, Vol. 54, Núm. 8, pp. 1231-1241
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Low aerobic capacity in McArdle disease: A role for mitochondrial network impairment?
Molecular metabolism, Vol. 66, pp. 101648
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Preclinical Research in McArdle Disease: A Review of Research Models and Therapeutic Strategies
Genes, Vol. 13, Núm. 1
2021
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The Second Wind in McArdle Patients: Fitness Matters
Frontiers in Physiology, Vol. 12
2020
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A DM1 family with interruptions associated with atypical symptoms and late onset but not with a milder phenotype
Human Mutation, Vol. 41, Núm. 2, pp. 420-431
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Absence of p.R50X Pygm read-through in McArdle disease cellular models
DMM Disease Models and Mechanisms, Vol. 13, Núm. 1
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Creation and implementation of a European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC registry)
Orphanet Journal of Rare Diseases, Vol. 15, Núm. 1
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Data from the European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC)
Orphanet Journal of Rare Diseases, Vol. 15, Núm. 1
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Preclinical research in glycogen storage diseases: A comprehensive review of current animal models
International Journal of Molecular Sciences, Vol. 21, Núm. 24, pp. 1-50
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Preliminary findings on ctg expansion determination in different tissues from patients with myotonic dystrophy type 1
Genes, Vol. 11, Núm. 11, pp. 1-8
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Sex differences and the influence of an active lifestyle on adiposity in patients with mcardle disease
International Journal of Environmental Research and Public Health, Vol. 17, Núm. 12, pp. 1-11
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The Influence of Basic Psychological Needs and Passion in Promoting Elite Young Football Players’ Development
Frontiers in Psychology, Vol. 11