المؤلفون: Nielsen, Joachim

المصدر: Nielsen , J 2023 , ' An experiment of nature links muscle glycogen unavailability with very high fat oxidation rates despite low aerobic fitness ' , Journal of Physiology , vol. 601 , no. 3 , pp. 389-390 . https://doi.org/10.1113/JP284098Test

مصطلحات موضوعية: exercise, fat metabolism, glycogen, McArdle disease, Oxidation-Reduction, Humans, Muscles, Exercise/physiology, Muscle, Skeletal/physiology, Glycogen/metabolism, Glycogen Storage Disease Type V/metabolism

العلاقة: https://portal.findresearcher.sdu.dk/da/publications/7f04d04c-7684-4d24-95a5-e000391d9027Test

الإتاحة: https://doi.org/10.1113/JP284098Test
https://portal.findresearcher.sdu.dk/da/publications/7f04d04c-7684-4d24-95a5-e000391d9027Test

المؤلفون: Nielsen, Tue L, Pinós, Tomàs, Brull, Astrid, Vissing, John, Krag, Thomas O

المصدر: Nielsen , T L , Pinós , T , Brull , A , Vissing , J & Krag , T O 2018 , ' Exercising with blocked muscle glycogenolysis : Adaptation in the McArdle mouse ' , Molecular Genetics and Metabolism , vol. 123 , no. 1 , pp. 21-27 . https://doi.org/10.1016/j.ymgme.2017.11.006Test

مصطلحات موضوعية: Animals, Disease Models, Animal, Glycogen/metabolism, Glycogen Storage Disease Type V/metabolism, Humans, Mice, Muscle, Skeletal/metabolism, Physical Conditioning

الإتاحة: https://doi.org/10.1016/j.ymgme.2017.11.006Test
https://curis.ku.dk/portal/da/publications/exercising-with-blocked-muscle-glycogenolysisTest(e95c018c-303c-4469-a819-07681467038a).html

المؤلفون: Marta Gonzalez-Freire, Joaquín Arenas, Alejandro Lucia, Juan C. Rubio, Antonio L. Andreu, Miguel A. Martín, Melissa Naidoo, LL Smith, Margarita Pérez

المصدر: Neuroscience Letters. 431:106-111

مصطلحات موضوعية: Adult, Male, Creatine Kinase/Blood, medicine.medical_specialty, Glycogenolysis, Inflammation, Biology, Fisiología humana, Systemic inflammation, Internal medicine, Myokine, medicine, Humans, Acute-Phase Reaction, Muscle, Skeletal, Creatine Kinase, Exercise, Enfermedad nutricional, Aged, Sedentary lifestyle, Analysis of Variance, General Neuroscience, Acute-phase protein, Middle Aged, Deporte, medicine.disease, Cytokines/Metabolism, Inflammation*/Physiopathology, Endocrinology, Glycogen Storage Disease Type V*/Physiopathology, Muscle, Skeletal/Metabolism, Myophosphorylase, Glycogen Storage Disease Type V*/Metabolism, Inflammation*/Metabolism, Inflammation*/Rehabilitation, Cytokines, Glycogen Storage Disease Type V, Female, medicine.symptom, Rhabdomyolysis, Glycogen Storage Disease Type V*/Rehabilitation

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef75c758dc55ec08bcce68d89dbd142aTest
https://doi.org/10.1016/j.neulet.2007.11.028Test

المؤلفون: González-Freire, Marta, Santiago Dorrego, Catalina, Gómez Gallego, Félix, Pérez Ruiz, Margarita, Foster, Carl, Arenas, Joaquín, Lucía Mulas, Alejandro

مصطلحات موضوعية: Genetic Predisposition To Disease/*Genetics, Glycogen Storage Disease Type V/*Genetics, Mutation/*Genetics, Myostatin/*Genetics, Amp Deaminase/Genetics, Dna Mutational Analysis, Exercise Tolerance/Genetics, Female, Genetic Variation/Genetics, Genotype, Glycogen/Metabolism, Glycogen Storage Disease Type V/Metabolism, Glycogen Storage Disease Type V/Physiopathology, Heterozygote, Humans, Muscle Weakness/Genetics, Muscle, Skeletal/Metabolism, Skeletal/Physiopathology, Peptidyl-Dipeptidase A/Genetics, Phenotype, Respiratory Insufficiency/Genetics, Enfermedad nutricional, Deporte, Tratamiento médico

العلاقة: González-Freire, M., Santiago-Dorrego, C., Gómez-Gallego, F., Pérez-Ruiz, M., Foster, C., Arenas, J., & Lucía-Mulas, A. (2009). Does the K153R variant of the myostatin gene influence the clinical presentation of women with McArdle disease? Neuromuscular Disorders, 19(3), 220-222.; http://hdl.handle.net/11268/1120Test

الإتاحة: https://doi.org/10.1016/j.nmd.2009.01.001Test
http://hdl.handle.net/11268/1120Test

المؤلفون: Lucía Mulas, Alejandro, Smith, Lucille, Naidoo, Melissa, González-Freire, Marta, Pérez Ruiz, Margarita, Rubio, Juan Carlos, Martín, Miguel Ángel, Andreu, Antoni L., Arenas, Joaquín

مصطلحات موضوعية: Exercise, Glycogen Storage Disease Type V*/Metabolism, Glycogen Storage Disease Type V*/Physiopathology, Glycogen Storage Disease Type V*/Rehabilitation, Inflammation*/Metabolism, Inflammation*/Physiopathology, Inflammation*/Rehabilitation, Analysis of Variance, Creatine Kinase/Blood, Cytokines/Metabolism, Female, Humans, Male, Middle Aged, Muscle, Skeletal/Metabolism, Enfermedad nutricional, Fisiología humana, Deporte

العلاقة: Lucía-Mulas, A., Smith, L., Naidoo, M., González-Freire, M., Pérez-Ruiz, M., Rubio, J. C., …, & Arenas, J. (2008). McArdle disease: another systemic low-inflammation disorder? Neuroscience Letters, 431(2), 106-111.; http://hdl.handle.net/11268/1119Test

الإتاحة: https://doi.org/10.1016/j.neulet.2007.11.028Test
http://hdl.handle.net/11268/1119Test

المؤلفون: Carl Foster, Joaquín Arenas, Alejandro Lucia, Félix Gómez-Gallego, Margarita Pérez, Catalina Santiago, Marta Gonzalez-Freire

مصطلحات موضوعية: DNA Mutational Analysis, Respiratory Insufficiency/Genetics, Myostatin, Disease, AMP Deaminase, Tratamiento médico, Genotype, Glycogen/Metabolism, Actinin, Genetics (clinical), Exercise Tolerance, Muscle Weakness, Exercise Tolerance/Genetics, biology, Muscle, Skeletal/Physiopathology, Genetic Variation/Genetics, Deporte, Dna Mutational Analysis, Phenotype, Neurology, Peptidyl-Dipeptidase A/Genetics, Female, medicine.symptom, Respiratory Insufficiency, Glycogen storage disease type V, Glycogen, Adult, Glycogen Storage Disease Type V/Physiopathology, medicine.medical_specialty, Heterozygote, Adolescent, Genetic Predisposition To Disease/*Genetics, Peptidyl-Dipeptidase A, Internal medicine, Genetic variation, Glycogen Storage Disease Type V/*Genetics, medicine, Myostatin/*Genetics, Humans, Genetic Predisposition to Disease, Muscle, Skeletal, Enfermedad nutricional, Muscle Weakness/Genetics, Aged, Muscle weakness, Genetic Variation, Cardiorespiratory fitness, Heterozygote advantage, medicine.disease, Endocrinology, Muscle, Skeletal/Metabolism, Amp Deaminase/Genetics, Pediatrics, Perinatology and Child Health, Mutation, biology.protein, Glycogen Storage Disease Type V, Neurology (clinical), Glycogen Storage Disease Type V/Metabolism, Mutation/*Genetics

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::539c42aa69b9ade0cc7de6f61a11a30dTest
https://hdl.handle.net/11268/1120Test

المصدر: Nielsen , T L , Pinós , T , Brull , A , Vissing , J & Krag , T O 2018 , ' Exercising with blocked muscle glycogenolysis : Adaptation in the McArdle mouse ' , Molecular Genetics and Metabolism , vol. 123 , no. 1 , pp. 21-27 .

مصطلحات الفهرس: Animals, Disease Models, Animal, Glycogen/metabolism, Glycogen Storage Disease Type V/metabolism, Humans, Mice, Muscle, Skeletal/metabolism, Physical Conditioning, Animal, article

URL: https://curis.ku.dk/portal/da/publications/exercising-with-blocked-muscle-glycogenolysisTest(e95c018c-303c-4469-a819-07681467038a).html
https://doi.org/10.1016/j.ymgme.2017.11.006Test