Bringing light into the darkness: autosomal recessive cerebellar ataxia due to a recessive mutation in the SEPSECS gene Á. Martínez-Martín; J. García-García; I. Díaz-Maroto Cicuéndez; M.L. Quintanilla-Mata; T. Segura;

Ocular myasthenia gravis and risk factors for developing a secondary generalisation: description of a Spanish series I. Díaz-Maroto; J. García-García; P.A. Sánchez-Ayaso; C. Alcahut-Rodríguez; E. González-Villar; J.M. Pardal-Fernández; T. Segura;

Calcified cerebral embolism: a 9-case series and review of the literature AJ. Mosqueira; B. Canneti; A. Martínez Calvo; P. Fernández Armendáriz; M. Seijo-Martinez; J.M. Pumar;