HiperCKemia paucisintomática secundaria a mutación en el gen ANO5 by C. Alcahut-Rodríguez, I. Díaz-Maroto, A. Fernández-Marmiesse, J. García-García

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Muscle weakness, joint laxity and keloids. A more than suggestive association by Á. Martínez-Martín, I. Díaz-Maroto Cicuéndez, J. Simón Sánchez, J. García-García

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Debilidad muscular, laxitud articular y queloides. Una asociación más que sugerente by Á. Martínez-Martín, I. Díaz-Maroto Cicuéndez, J. Simón Sánchez, J. García-García

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A series of patients with refractory myasthenia gravis by J. Garcia-Garcia, I. Díaz-Maroto, A. Martínez-Martín, J.M. Pardal-Fernández, T. Segura

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

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Aportando luz en la oscuridad: ataxia cerebelosa autosómica recesiva por mutación en el gen SEPSECS by Á. Martínez-Martín, J. García-García, I. Díaz-Maroto Cicuéndez, M.L. Quintanilla-Mata, T. Segura

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

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Has the aetiology of ischaemic stroke changed in the past decades? Analysis and comparison of data from current and historical stroke databases by Á. Sánchez-Larsen, J. García-García, O. Ayo-Martín, F. Hernández-Fernández, I. Díaz-Maroto, E. Fernández-Díaz, M. Monteagudo, T. Segura

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