M Pineda

[Familiar chronic progressive external ophthalmoplegia of mitochondrial origin].

R. Artuch, M. Pineda, J. Montoya, 2004, Revista de neurologia.

Molecular characterization of 3-phosphoglycerate dehydrogenase deficiency--a neurometabolic disorder associated with reduced L-serine biosynthesis.

R Berger, M. Durán, M. Pineda, 2000, American journal of human genetics.

Friedreich's ataxia: idebenone treatment in early stage patients.

E. Monrós, R. Artuch, M. Pineda, 2002, Neuropediatrics.