Publicaciones en las que colabora con Eduardo Ruiz Pesini (6)

2020

  1. A novel mutation in the mitochondrial MT-ND5 gene in a family with MELAS. The relevance of genetic analysis on targeted tissues

    Mitochondrion, Vol. 50, pp. 14-18

2016

  1. Secondary coenzyme Q10 deficiencies in oxidative phosphorylation (OXPHOS) and non-OXPHOS disorders

    Mitochondrion, Vol. 30, pp. 51-58

2014

  1. Follow-up of folinic acid supplementation for patients with cerebral folate deficiency and Kearns-Sayre syndrome

    Orphanet journal of rare diseases, Vol. 9, pp. 217

2008

  1. Mitochondrial DNA background modulates the assembly kinetics of OXPHOS complexes in a cellular model of mitochondrial disease

    Human Molecular Genetics, Vol. 17, Núm. 24, pp. 4001-4011

1999

  1. Respiratory chain enzyme activities in spermatozoa from untreated Parkinson's disease patients

    Journal of Neural Transmission, Vol. 106, Núm. 9-10, pp. 919-924

1998

  1. Correlation of sperm motility with mitochondrial enzymatic activities

    Clinical Chemistry, Vol. 44, Núm. 8 I, pp. 1616-1620