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Campos Y
Campos Y
Research Scientist, Mitochondrial Pathology Unit, Instituto de Salud Carlos III
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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
5612008
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
2161998
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
2002005
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
1332015
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
1302013
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
1202005
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
1151993
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
1132001
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
1072004
Biological roles of L-carnitine in perinatal metabolism
J Arenas, JC Rubio, MA Martı́n, Y Campos
Early human development 53, S43-S50, 1998
1041998
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
1022005
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
1021993
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
992005
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
961994
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
921997
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
912009
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
902004
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
881992
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
851997
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
822003
El sistema no puede realizar la operación en estos momentos. Inténtalo de nuevo más tarde.
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