Universidad de Zaragoza-ko ikertzaileekin lankidetzan egindako argitalpenak (9)

2019

  1. Muscle involvement in a large cohort of pediatric patients with genetic diagnosis of mitochondrial disease

    Journal of Clinical Medicine, Vol. 8, Núm. 1

2016

  1. A statistical algorithm showing coenzyme Q10 and citrate synthase as biomarkers for mitochondrial respiratory chain enzyme activities

    Scientific Reports, Vol. 6, Núm. 1

  2. Secondary coenzyme Q10 deficiencies in oxidative phosphorylation (OXPHOS) and non-OXPHOS disorders

    Mitochondrion, Vol. 30, pp. 51-58

  3. Severe encephalopathy associated to pyruvate dehydrogenase mutations and unbalanced coenzyme Q 10 content

    European Journal of Human Genetics, Vol. 24, Núm. 3, pp. 367-372

  4. The CoQH2/CoQ Ratio Serves as a Sensor of Respiratory Chain Efficiency

    Cell Reports, Vol. 15, Núm. 1, pp. 197-209

2013

  1. Coenzyme Q10 deficiency in mitochondrial DNA depletion syndromes

    Mitochondrion, Vol. 13, Núm. 4, pp. 337-341

  2. Supercomplex assembly determines electron flux in the mitochondrial electron transport chain

    Science, Vol. 340, Núm. 6140, pp. 1567-1570

2009

  1. Coenzyme Q10 deficiency associated with a mitochondrial DNA depletion syndrome: A case report

    Clinical Biochemistry, Vol. 42, Núm. 7-8, pp. 742-745

2005

  1. Muscle coenzyme Q10 concentrations in patients with probable and definite diagnosis of respiratory chain disorders

    BioFactors