Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Eulalia Turon‐Viñas"'
Autor:
Susana Boronat, Eulalia Turon‐Viñas, Noel Mac Manus, Asuncion Diaz‐Gomez, Mónica Vicente, Victoria Ros‐Castelló, Alba Sierra‐Marcos
Publikováno v:
Epilepsia Open, Vol 9, Iss 6, Pp 2505-2509 (2024)
Abstract Type I Alexander disease (AxD) presents with paroxysmal neurodegeneration, refractory epilepsy, and encephalopathy in the first years of life and is associated with a poor prognosis. Although there is no treatment, mild symptomatic improveme
Externí odkaz:
https://doaj.org/article/31442da6b42c4c98a6f988bd8932da1f
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:
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:
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 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
Externí odkaz:
https://doaj.org/article/cd5b7b0069af4fba957e91daa63624be