E. Rivas Infante

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

P. Navas, E. Ruiz-Pesini, E. Trevisson, 2016, Mitochondrion.

A novel dominant mutation in CRYAB gene leading to a severe phenotype with childhood onset

A. T. Marcos, F. Galán, J. Navarro-Pando, 2020, Molecular genetics & genomic medicine.

Screening of effective pharmacological treatments for MELAS syndrome using yeasts, fibroblasts and cybrid models of the disease

M. Álvarez-Dolado, P. Navas, S. Francisci, 2012, British journal of pharmacology.

Cricopharyngeal myotomy in the treatment of oculopharyngeal muscular dystrophy.

F. Esteban Ortega, Antonio Gómez-Torres, I. Tirado Zamora, 2012, Acta otorrinolaringologica espanola.

Neuropeptides in the developing human hippocampus under hypoxic–ischemic conditions

E. Rivas Infante, S. Cebada Sánchez, Marı’a del Mar Arroyo Jiménez, 2021, Journal of anatomy.

[Cerebral amyloid angiopathy, recurrent intracerebral haemorrhages and Down's syndrome].

J. L. Maciñeiras Montero, E. Rivas Infante, J. Romero López, 2006, Neurologia.