Julio
Montoya Villaroya
Julio Montoya Villaroya-rekin lankidetzan egindako argitalpenak (8)
2019
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Muscle involvement in a large cohort of pediatric patients with genetic diagnosis of mitochondrial disease
Journal of Clinical Medicine, Vol. 8, Núm. 1
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Plasma coenzyme Q10 status is impaired in selected genetic conditions
Scientific Reports, Vol. 9, Núm. 1
2016
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A statistical algorithm showing coenzyme Q10 and citrate synthase as biomarkers for mitochondrial respiratory chain enzyme activities
Scientific Reports, Vol. 6, Núm. 1
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Secondary coenzyme Q10 deficiencies in oxidative phosphorylation (OXPHOS) and non-OXPHOS disorders
Mitochondrion, Vol. 30, pp. 51-58
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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
2013
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Coenzyme Q10 deficiency in mitochondrial DNA depletion syndromes
Mitochondrion, Vol. 13, Núm. 4, pp. 337-341
2009
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Coenzyme Q10 deficiency associated with a mitochondrial DNA depletion syndrome: A case report
Clinical Biochemistry, Vol. 42, Núm. 7-8, pp. 742-745