Search Results - "Villaverde, F. Julián"

Impact of COVID‐19 outbreak in reperfusion therapies of acute ischaemic stroke in northwest Spain by Tejada Meza, H., Lambea Gil, Á., Sancho Saldaña, A., Martínez‐Zabaleta, M., Garmendia Lopetegui, E., López‐Cancio Martínez, E., Castañón Apilánez, M., Herrera Isasi, M., Marta Enguita, J., Gómez‐Vicente, B., Arenillas, J.F., Arenaza Basterrechea, N., Timiraos Fernández, J.J., Sánchez Herrero, J., Maciñeiras Montero, J.L., Castellanos Rodrigo, M., Fernández‐Coud, D., Casado Menéndez, I., Temprano Fernández, M.T., Freijo, M., Luna, A., Palacio Portilla, E.J., Jiménez López, Y., Rodríguez‐Castro, E., Rodríguez‐Yáñez, M., Tejada García, J., Beltrán Rodríguez, I., Julián‐Villaverde, F., Moreno García, M.P., Trejo Gabriel‐Galán, J.M., Echavarría Iñiguez, A., Pérez Lázaro, C., Navarro Pérez, M.P., Marta Moreno, J.

“…Background and purpose Spain has been one of the countries more heavily stricken by SARS‐CoV‐2, which has had huge implications for stroke care. The aim was to…”
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Incidence and outcoMes of MInor stroke and high-risk traNsient ischEmic attack in NordicTus. IMMINENT study by Ramos-Araque, M.E., Castellanos, M., Naya Rios, L., López-Cancio, E., Molina Gil, J., Marta-Moreno, J., Tejada-Meza, H., Temprano Fernández, M., Antón González, C., Vidal de Francisco, D., Tejada-García, J., Maciñeiras Montero, J.L., Vicente Alba, P., García-Sánchez, J.M., Aguilera Irazabal, B., Martínez-Zabaleta, M., Diez, I.N., Pinedo Brochado, A., Azkune Calle, I., Freijo, M.M., Moreno-Estebanez, A., Palacio-Portilla, E., Manrique Arregui, L., Rodríguez-Yáñez, M., Santamaría-Cadavid, M., Timiraos-Fernández, J.J., Herrero Infante, Y., Trejo-Gabriel-Galán, J., Echavarria-Iñiguez, A., Tejero-Juste, C., Rodríguez Montolio, J., Julián-Villaverde, F., Moreno García, M., López-Mesonero, L., Redondo-Robles, L., Aymerich, N., Korroza, J., Arenillas, J.F.

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Fatal familial insomnia (FFI) in Basque country. Clinical manifestations, polysomnographic patterns and pathologic findings in three cases by Guerra, A. Asencio, De Larrinaga, A. Alvarez Ruiz, Santaolalla, C. Egea, Cantolla, J. Durán, Vadillo, E. Alvarez, Villaverde, F. Julián

“…Introduction The FFI is a rare prion disease, originated by the mutation D178N in the PRNP gene. It has an autosomal dominant inheritance pattern. Patients…”
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