Publicacions en què col·labora amb Diana Reche López (12)
2023
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Actin Polymerization Defects Induce Mitochondrial Dysfunction in Cellular Models of Nemaline Myopathies
Antioxidants, Vol. 12, Núm. 12
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Alpha-lipoic acid supplementation corrects pathological alterations in cellular models of pantothenate kinase-associated neurodegeneration with residual PANK2 expression levels
Orphanet journal of rare diseases, Vol. 18, Núm. 1, pp. 80
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Antioxidants Prevent Iron Accumulation and Lipid Peroxidation, but Do Not Correct Autophagy Dysfunction or Mitochondrial Bioenergetics in Cellular Models of BPAN
International Journal of Molecular Sciences, Vol. 24, Núm. 19
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Mitochondrial Quality Control via Mitochondrial Unfolded Protein Response (mtUPR) in Ageing and Neurodegenerative Diseases
Biomolecules, Vol. 13, Núm. 12
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Neurodegeneration, Mitochondria, and Antibiotics
Metabolites, Vol. 13, Núm. 3
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Patient-Derived Cellular Models for Polytarget Precision Medicine in Pantothenate Kinase-Associated Neurodegeneration
Pharmaceuticals, Vol. 16, Núm. 10
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Vicious cycle of lipid peroxidation and iron accumulation in neurodegeneration
Neural Regeneration Research, Vol. 18, Núm. 6, pp. 1196-1202
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mtUPR Modulation as a Therapeutic Target for Primary and Secondary Mitochondrial Diseases
International Journal of Molecular Sciences, Vol. 24, Núm. 2
2022
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Activation of the Mitochondrial Unfolded Protein Response: A New Therapeutic Target?
Biomedicines, Vol. 10, Núm. 7
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Pantothenate and L-Carnitine Supplementation Improves Pathological Alterations in Cellular Models of KAT6A Syndrome
Genes, Vol. 13, Núm. 12
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Therapeutic approach with commercial supplements for pantothenate kinase-associated neurodegeneration with residual PANK2 expression levels
Orphanet journal of rare diseases, Vol. 17, Núm. 1, pp. 311
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UPRmt activation improves pathological alterations in cellular models of mitochondrial diseases
Orphanet Journal of Rare Diseases, Vol. 17, Núm. 1