M. Lara

Targeted impairment of thymidine kinase 2 expression in cells induces mitochondrial DNA depletion and reveals molecular mechanisms of compensation of mitochondrial respiratory activity.

A. Meseguer, E. García-Arumí, J. Villarroya, 2011, Biochemical and biophysical research communications.

Hearing Loss in a Patient With the Myopathic Form of Mitochondrial DNA Depletion Syndrome and a Novel Mutation in the TK2 Gene

E. Ruiz-Pesini, M. Pineda, J. Montoya, 2010, Pediatric Research.

Unchanged thymidine triphosphate pools and thymidine metabolism in two lines of thymidine kinase 2‐mutated fibroblasts

V. Bianchi, C. Rampazzo, M. R. Vilá, 2009, The FEBS journal.

Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE): Biochemical Features and Therapeutic Approaches

M. Valentino, M. Hirano, R. Martí, 2007, Bioscience reports.

Infusion of platelets transiently reduces nucleoside overload in MNGIE

Y. Anikster, B. Weiss, A. Andreu, 2006, Neurology.

Cognitive dysfunction and hypogonadotrophic hypogonadism in a Brazilian patient with mitochondrial neurogastrointestinal encephalomyopathy and a novel ECGF1 mutation

E. Ruiz-Pesini, J. Montoya, F. J. Carod-Artal, 2007, European journal of neurology.

A novel thymidine phosphorylase mutation in a Spanish MNGIE patient

F. Mearin, A. Andreu, J. Gámez, 2005, Journal of the Neurological Sciences.

Increased muscle nucleoside levels associated with a novel frameshift mutation in the thymidine phosphorylase gene in a Spanish patient with MNGIE

J. Arenas, A. Andreu, R. Garesse, 2005, Neuromuscular Disorders.

Lack of gastrointestinal symptoms in a 60-year-old patient with MNGIE

J. Arenas, A. Andreu, Y. Campos, 2004, Neurology.