M. Martín

发表

Sporadic MERRF/MELAS overlap syndrome associated with the 3243 tRNALeu(UUR) mutation of mitochondrial DNA

J. Arenas, Miguel Ángel Martín, Y. Campos, 1996, Muscle & nerve.

Myocardial carnitine and carnitine palmitoyltransferase deficiencies in patients with severe heart failure.

J. Arenas, M. Gomez, Y. Campos, 2000, Biochimica et biophysica acta.

Mitochondrial myopathy, cardiomyopathy and psychiatric illness in a Spanish family harbouring the mtDNA 3303C > T mutation

M. Castro‐Gago, J. Arenas, M. Fuster, 2001, Journal of Inherited Metabolic Disease.

Single large-scale mitochondrial DNA deletion in a patient with mitochondrial myopathy associated with multiple symmetric lipomatosis

J. Arenas, Miguel Ángel Martín, C. Navarro, 1996, Neurology.

Respiratory chain enzyme activities in isolated mitochondria of lymphocytes from patients with Alzheimer's disease

J. Benito-León, F. Jiménez-Jiménez, M. Ortı́-Pareja, 1997, Neurology.

Leigh syndrome associated with the T9176C mutation in the ATPase 6 gene of mitochondrial DNA

J. Terradas, J. Arenas, Y. Campos, 1997, Neurology.

Can patients with McArdle’s disease run?

A. Lucia, M. Pérez, J. Arenas, 2006, British Journal of Sports Medicine.

Biological roles of L-carnitine in perinatal metabolism.

J. Arenas, Y. Campos, M. Martín, 1998, Early human development.

Molecular analysis of the superoxide dismutase 1 gene in Spanish patients with sporadic or familial amyotrophic lateral sclerosis

J. Arenas, F. Cañadillas, F. Bustos, 2002, Muscle & nerve.

Exercise capacity in a 78 year old patient with McArdle’s disease: it is never too late to start exercising

Margarita Pérez, A. Lucia, M. Pérez, 2006, British Journal of Sports Medicine.

211th ENMC International Workshop: Development of diagnostic criteria and management strategies for McArdle Disease and related rare glycogenolytic disorders to improve standards of care. 17–19 April 2015, Naarden, The Netherlands

P. Laforêt, J. Vissing, B. Schoser, 2017, Neuromuscular Disorders.

Molecular analysis of Spanish patients with AMP deaminase deficiency

J. Arenas, Miguel Ángel Martín, C. Navarro, 2000, Muscle & nerve.

AMPD1 Genotypes and Exercise Capacity in McArdle Patients

A. Lucia, M. Pérez, J. Arenas, 2007, International journal of sports medicine.

Mitochondrial dysfunction associated with a mutation in the Notch3 gene in a CADASIL family

J. Molina, B. Bornstein, J. Arenas, 2001, Neurology.

Natural disease course and genotype-phenotype correlations in Complex I deficiency caused by nuclear gene defects: what we learned from 130 cases

M. Tarnopolsky, R. Rodenburg, M. Knaap, 2012, Journal of Inherited Metabolic Disease.

Abnormal carnitine distribution in the muscles of patients with idiopathic inflammatory myopathy.

J. Gómez-Reino, J. Arenas, M. R. Gonzalez-Crespo, 1996, Arthritis and rheumatism.

Non-osteogenic muscle hypertrophy in children with McArdle disease

I. Ara, L. Alegre, A. Santalla, 2018, Journal of Inherited Metabolic Disease.

Effect of nitric oxide on mitochondrial respiratory activity of human articular chondrocytes

M. D. de Andrés, J. Arenas, F. Blanco, 2004, Annals of the rheumatic diseases.

Mobilisation of mesenchymal cells into blood in response to skeletal muscle injury

A. Lucia, J. Arenas, A. Andreu, 2006, British Journal of Sports Medicine.