OPA1 mutations induce mitochondrial DNA instability and optic atrophy ‘plus’ phenotypes P Amati-Bonneau, ML Valentino, P Reynier, ME Gallardo, B Bornstein, ... Brain 131 (2), 338-351, 2008 | 562 | 2008 |
Complex I defect in muscle from patients with Huntington's disease J Arenas, Y Campos, R Ribacoba, MA Martín, JC Rubio, P Ablanedo, ... Annals of neurology 43 (3), 397-400, 1998 | 220 | 1998 |
Specific correlation between the wobble modification deficiency in mutant tRNAs and the clinical features of a human mitochondrial disease Y Kirino, Y Goto, Y Campos, J Arenas, T Suzuki Proceedings of the National Academy of Sciences 102 (20), 7127-7132, 2005 | 201 | 2005 |
Regulated lysosomal exocytosis mediates cancer progression E Machado, S White-Gilbertson, D van de Vlekkert, L Janke, S Moshiach, ... Science advances 1 (11), e1500603, 2015 | 135 | 2015 |
Identification and characterization of the nano-sized vesicles released by muscle cells DP Romancino, G Paterniti, Y Campos, A De Luca, V Di Felice, A d’Azzo, ... FEBS letters 587 (9), 1379-1384, 2013 | 130 | 2013 |
Renal pathology in children with mitochondrial diseases E Martín-Hernández, MT García-Silva, J Vara, Y Campos, A Cabello, ... Pediatric nephrology 20, 1299-1305, 2005 | 120 | 2005 |
Plasma carnitine insufficiency and effectiveness of L‐carnitine therapy in patients with mitochondril myopathy Y Campos, R Huertas, G Lorenzo, J Bautista, E Gutierrez, M Aparicio, ... Muscle & Nerve: Official Journal of the American Association of …, 1993 | 115 | 1993 |
Molecular heterogeneity of myophosphorylase deficiency (McArdle's disease): a genotype‐phenotype correlation study MA Martín, JC Rubio, J Buchbinder, R Fernández‐Hojas, P Del Hoyo, ... Annals of Neurology: Official Journal of the American Neurological …, 2001 | 114 | 2001 |
Ozz-E3, a muscle-specific ubiquitin ligase, regulates β-catenin degradation during myogenesis T Nastasi, A Bongiovanni, Y Campos, L Mann, JN Toy, J Bostrom, ... Developmental cell 6 (2), 269-282, 2004 | 108 | 2004 |
Biological roles of L-carnitine in perinatal metabolism J Arenas, JC Rubio, MA Martı́n, Y Campos Early human development 53, S43-S50, 1998 | 105 | 1998 |
Respiratory chain enzyme activities in lymphocytes from untreated patients with Parkinson disease N Barroso, Y Campos, R Huertas, J Esteban, JA Molina, A Alonso, ... Clinical chemistry 39 (4), 667-669, 1993 | 104 | 1993 |
Exercise training in mitochondrial myopathy: a randomized controlled trial P Cejudo, J Bautista, T Montemayor, R Villagómez, L Jiménez, F Ortega, ... Muscle & Nerve: Official Journal of the American Association of …, 2005 | 102 | 2005 |
Leigh syndrome associated with mitochondrial complex I deficiency due to a novel mutation in the NDUFS1 gene MA Martín, A Blázquez, LG Gutierrez-Solana, D Fernández-Moreira, ... Archives of neurology 62 (4), 659-661, 2005 | 100 | 2005 |
Effects of l‐carnitine on the pyruvate dehydrogenase complex and carnitine palmitoyl transferase activities in muscle of endurance athletes J Arenas, R Huertas, Y Campos, AE Díaz, JM Villalón, E Vilas FEBS letters 341 (1), 91-93, 1994 | 97 | 1994 |
Leigh syndrome associated with the T9176C mutation in the ATPase 6 gene of mitochondrial DNA Y Campos, MA Martin, JC Rubio, LG Solana, C Garcia-Benayas, ... Neurology 49 (2), 595-597, 1997 | 92 | 1997 |
Heterodimerization of the sialidase NEU1 with the chaperone protective protein/cathepsin A prevents its premature oligomerization EJ Bonten, Y Campos, V Zaitsev, A Nourse, B Waddell, W Lewis, G Taylor, ... Journal of biological chemistry 284 (41), 28430-28441, 2009 | 91 | 2009 |
Coenzyme Q 10 improves lactic acidosis, strokelike episodes, and epilepsy in a patient with MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes) A Berbel-Garcia, JR Barbera-Farre, JP Etessam, AM Salio, A Cabello, ... Clinical neuropharmacology 27 (4), 187-191, 2004 | 91 | 2004 |
Respiratory chain enzymes in muscle of endurance athletes: effect of L-carnitine R Huertas, Y Campos, E Díaz, J Esteban, L Vechietti, G Montanari, ... Biochemical and biophysical research communications 188 (1), 102-107, 1992 | 89 | 1992 |
Bilateral striatal necrosis and MELAS associated with a new T3308C mutation in the mitochondrial ND1 gene Y Campos, MA Martı́n, JC Rubio, MCG del Olmo, A Cabello, J Arenas Biochemical and biophysical research communications 238 (2), 323-325, 1997 | 86 | 1997 |
Prevalence and progression of mitochondrial diseases: a study of 50 patients J Arpa, A Cruz‐Martínez, Y Campos, M Gutiérrez‐Molina, F García‐Rio, ... Muscle & nerve 28 (6), 690-695, 2003 | 83 | 2003 |