Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Eulàlia Turón-Viñas"'
Autor:
Elba Pascual-Goñi, Maria Josa, Cristian Launes, Luis Querol, Marga del Cuerpo, M. Alba Bosch, Iolanda Jordan, Eulàlia Turón-Viñas
Publikováno v:
Frontiers in Neurology, Vol 10 (2019)
The clinical spectrum of Enterovirus-71-associated neurological disease includes acute flaccid paralysis, encephalomyelitis, or brainstem encephalitis with autonomic dysfunction. As no specific antiviral treatments are available, intravenous human im
Externí odkaz:
https://doaj.org/article/9f3db2e5501e4a91a92360960184e2ff
Autor:
Eulàlia Turón-Viñas, Mercè Pineda, Victòria Cusí, Eduardo López-Laso, Rebeca Losada del Pozo, Luis González Gutiérrez-Solana, David Conejo Moreno, Concha Sierra-Córcoles, Naiara Olabarrieta-Hoyos, Marcos Madruga-Garrido, Javier Aguirre-Rodríguez, Verónica González-Álvarez, Mar O’Callaghan, Jordi Muchart, Judith Armstrong-Moron
Publikováno v:
Journal of Central Nervous System Disease, Vol 2014, Iss 6, Pp 59-68 (2014)
Externí odkaz:
https://doaj.org/article/7d82afabc4a44215a8fb849d52ef7c8b
Autor:
Fátima Castillo, Eulàlia Turón-Viñas, Laura Armendariz, Emma Carbonell, Nuria Rabella, Margarita del Cuerpo, Elisenda Moliner
Publikováno v:
Enfermedades Infecciosas y Microbiología Clínica.
Autor:
Eulàlia Turón-Viñas, Susana Boronat, Maria Trabazo, Sònia Brió, Elisabet Coca, Georgina Morón-Cazalilla, Isabel Badell
Publikováno v:
JOURNAL OF CHILD NEUROLOGY
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Neurologic complications following stem cell transplantation are of utmost importance owing to their high morbimortality. Although many studies have been performed in the adult population, reports in children are scarce. Our objective was to determin
Autor:
Chiara Cavestro, Francesca Morra, Andrea Legati, Marco D'Amato, Alessia Nasca, Arcangela Iuso, Naomi Lubarr, Jennifer L. Morrison, Patricia G. Wheeler, Clara Serra‐Juhé, Benjamín Rodríguez‐Santiago, Eulalia Turón‐Viñas, Clement Prouteau, Magalie Barth, Susan J. Hayflick, Daniele Ghezzi, Valeria Tiranti, Ivano Di Meo
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 11, Iss 6, Pp 1615-1629 (2024)
Abstract Objective COASY, the gene encoding the bifunctional enzyme CoA synthase, which catalyzes the last two reactions of cellular de novo coenzyme A (CoA) biosynthesis, has been linked to two exceedingly rare autosomal recessive disorders, such as
Externí odkaz:
https://doaj.org/article/57f4965baaa6402db85985dc9844f841
Autor:
Eulàlia Turón Viñas, Fatima Castillo Gómez, Elisenda Moliner Calderón, Laura Armendáriz Lacasa, Emma Carbonell Estarellas, Margarita del Cuerpo Casas, Nuria Rabella Garcia
Enteroviruses are a type of RNA-strained virus with more than 100 different genotypes. Infection can be asymptomatic, or symptoms can range from mild to severe. Some patients can develop neurological involvement, such as aseptic meningitis, encephali
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::606e84b89332d3ab49f5b193382f5a58
https://doi.org/10.21203/rs.3.rs-1258816/v1
https://doi.org/10.21203/rs.3.rs-1258816/v1
Autor:
Asunción Díaz-Gómez, Elisabet Coca, Eulàlia Turón-Viñas, Lucía Dougherty, Carlos Ruiz, Susana Boronat
Publikováno v:
Child Neurology Open, Vol 8 (2021)
Child Neurology Open
Child Neurology Open
Dravet syndrome is a genetic developmental and epileptic encephalopathy (DEE) mostly due to mutations in SCN1A gene. Perampanel is a selective and non-competitive alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor antagonist. Th
Autor:
Naiara Olabarrieta-Hoyos, Veronica Gonzalez-Alvarez, Mar O'Callaghan, Victoria Cusi, Rebeca Losada-Del Pozo, Eulàlia Turón-Viñas, David Conejo Moreno, Javier Aguirre-Rodríguez, Judith Armstrong-Moron, Concha Sierra-Córcoles, Mercè Pineda, Luis González Gutiérrez-Solana, Eduardo López-Laso, Marcos Madruga-Garrido, Jordi Muchart
Publikováno v:
Journal of Central Nervous System Disease, Vol 2014, Iss 6, Pp 59-68 (2014)
Journal of Central Nervous System Disease
Journal of Central Nervous System Disease, Vol 6 (2014)
Journal of Central Nervous System Disease
Journal of Central Nervous System Disease, Vol 6 (2014)
Vanishing white matter (VWM) leukoencephalopathy is one of the most prevalent hereditary white matter diseases. It has been associated with mutations in genes encoding eukaryotic translation initiation factor ( eIF2B). We have compiled a list of all
Autor:
JC Flores-Gonzalez, Eider Onate-Vergara, Eulàlia Turón-Viñas, Cristina Montero-Valladares, J.P. García-Íñiguez, Cinta Tellez-Gonzalez, Francisco Fernández-Carrión, Antonio Rodríguez-Núñez, Iolanda Jordan-Garcia
Publikováno v:
Revista de Neurología. 62:240
Autor:
Eulàlia, Turón-Viñas, Anna, López-Casas, Andrea, Palacio-Navarro, Antonio, Donaire, Gemma, García-Fructuoso, Jordi, Rumià, Victoria, Cusí-Sánchez, Francesc X, Sanmartí
Publikováno v:
Revista de neurologia. 51(8)
The epilepsy monitoring unit is a space inside a hospital, which objective is to reproduce epileptic seizures in order to better study of an epileptic patient. We have analysed data from all the patients admitted to our pediatric epilepsy unit in the