Antoni Barrientos

Sporadic heteroplasmic single 5.5 Kb mitochondrial DNA deletion associated with cerebellar ataxia, hypogonadotropic hypogonadism, choroidal dystrophy, and mitochondrial respiratory chain complex I deficiency

X. Estivill, J. Fernández-Real, J. Grau, 1997, Human mutation.

Autosomal recessive Wolfram syndrome associated with an 8.5-kb mtDNA single deletion.

X. Estivill, E. Tolosa, V. Volpini, 1996, American journal of human genetics.

A nuclear defect in the 4p16 region predisposes to multiple mitochondrial DNA deletions in families with Wolfram syndrome.

X. Estivill, V. Volpini, I. Ferrer, 1996, The Journal of clinical investigation.

Mitochondrial function in heart muscle from patients with idiopathic dilated cardiomyopathy.

Ò. Miró, C. Moraes, A. Barrientos, 2000, Cardiovascular research.

Biochemical parameters for the diagnosis of mitochondrial respiratory chain deficiency in humans, and their lack of age-related changes.

A. Munnich, P. Rustin, A. Rötig, 1998, The Biochemical journal.

Effects of general anaesthetic procedures on mitochondrial function of human skeletal muscle

Ò. Miró, A. Barrientos, F. Cardellach, 1999, European Journal of Clinical Pharmacology.