Miguel Angel Martin Casanueva
Miguel Angel Martin Casanueva
Hospital Universitario 12 de Octubre. Instituto de Investigación i+12
Dirección de correo verificada de h12o.es
TítuloCitado porAño
Defective hepatic mitochondrial respiratory chain in patients with nonalcoholic steatohepatitis
M Pérez-Carreras, P Del Hoyo, MA Martın, JC Rubio, A Martın, ...
Hepatology 38 (4), 999-1007, 2003
5942003
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, 2007
4102007
Mitochondrial complex I plays an essential role in human respirasome assembly
D Moreno-Lastres, F Fontanesi, I García-Consuegra, MA Martín, J Arenas, ...
Cell metabolism 15 (3), 324-335, 2012
1972012
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
1741998
Mitochondrial respiratory activity is altered in osteoarthritic human articular chondrocytes
E Maneiro, MA Martín, MC de Andres, MJ López‐Armada, ...
Arthritis & Rheumatism 48 (3), 700-708, 2003
1702003
Mitochondrial DNA background modulates the assembly kinetics of OXPHOS complexes in a cellular model of mitochondrial disease
R Pello, MA Martín, V Carelli, LG Nijtmans, A Achilli, M Pala, A Torroni, ...
Human molecular genetics 17 (24), 4001-4011, 2008
1452008
McArdle disease: what do neurologists need to know?
A Lucia, G Nogales-Gadea, M Pérez, MA Martín, AL Andreu, J Arenas
Nature Reviews Neurology 4 (10), 568, 2008
1252008
X‐linked NDUFA1 gene mutations associated with mitochondrial encephalomyopathy
D Fernandez‐Moreira, C Ugalde, R Smeets, RJT Rodenburg, ...
Annals of neurology 61 (1), 73-83, 2007
1252007
Effect of nitric oxide on mitochondrial respiratory activity of human articular chondrocytes
E Maneiro, MJ Lopez-Armada, MC De Andres, B Carames, MA Martin, ...
Annals of the rheumatic diseases 64 (3), 388-395, 2005
1202005
Mitochondrial respiratory chain dysfunction: implications in neurodegeneration
M Morán, D Moreno-Lastres, L Marín-Buera, J Arenas, MA Martín, ...
Free Radical Biology and Medicine 53 (3), 595-609, 2012
1192012
Genotypic and phenotypic features of McArdle disease: insights from the Spanish national registry
A Lucia, JR Ruiz, A Santalla, G Nogales-Gadea, JC Rubio, ...
J Neurol Neurosurg Psychiatry 83 (3), 322-328, 2012
1012012
Mitochondrial activity is modulated by TNFα and IL-1β in normal human chondrocyte cells
MJ López-Armada, B Carames, MA Martin, B Cillero-Pastor, M Lires-Dean, ...
Osteoarthritis and cartilage 14 (10), 1011-1022, 2006
1012006
Frequency of the C34T mutation of the AMPD1 gene in world-class endurance athletes: does this mutation impair performance?
JC Rubio, MA Martín, M Rabadán, F Gómez-Gallego, AF San Juan, ...
Journal of Applied Physiology 98 (6), 2108-2112, 2005
962005
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
952001
Natural disease course and genotype-phenotype correlations in Complex I deficiency caused by nuclear gene defects: what we learned from 130 cases
S Koene, RJ Rodenburg, MS Van Der Knaap, M Willemsen, W Sperl, ...
Journal of inherited metabolic disease 35 (5), 737-747, 2012
892012
Renal pathology in children with mitochondrial diseases
E Martín-Hernández, MT García-Silva, J Vara, Y Campos, A Cabello, ...
Pediatric nephrology 20 (9), 1299-1305, 2005
872005
Mitochondrial respiration controls lysosomal function during inflammatory T cell responses
F Baixauli, R Acín-Pérez, C Villarroya-Beltrí, C Mazzeo, N Nuñez-Andrade, ...
Cell metabolism 22 (3), 485-498, 2015
862015
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
842005
Favorable responses to acute and chronic exercise in McArdle patients
JL Maté-Munoz, M Moran, M Pérez, C Chamorro-Vina, F Gómez-Gallego, ...
Clinical Journal of Sport Medicine 17 (4), 297-303, 2007
832007
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
801997
El sistema no puede realizar la operación en estos momentos. Inténtalo de nuevo más tarde.
Artículos 1–20