E. M. Martínez Fernández

Clinical and molecular characterization of hereditary spastic paraplegia in a spanish Southern region

C. Méndez del Barrio, J. Oropesa, I. Royo, 2020, The International journal of neuroscience.

Unusual clinical presentation and new mutation in a case of triple A syndrome.

P. Carrasco Salas, E. M. Martínez Fernández, María Eugenia López Valverde, 2022, Endocrinologia, diabetes y nutricion.

Epidemiology of ataxia and hereditary spastic paraplegia in Spain: a cross-sectional study.

T. Segura Martín, M. Bártulos Iglesias, C. González Mingot, 2021, Neurologia.

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

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