Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Luis Gutiérrez-Solana"'
Autor:
Dídac Casas-Alba, Anna Aguilar, Itziar Alonso, María Teresa García, Maria Roberta Cilio, Carmen Fons, Javier López-Pisón, Luis Gutiérrez-Solana, Fernando Ferragut, María Luz Ruiz-Falcó, Víctor Soto-Insuga, Elena González, Tamara Pablos, María José Mas, Sara Hernández, María Vázquez-López, Patricia Fuentes-Pita, Sergio Aguilera-Albesa, Rocío Sánchez-Carpintero, Montserrat Garcia-Puig, Deyanira García-Navas, Helena Alarcón-Martínez, Candelaria González, Rocío Calvo, Ana Extraviz, Jordi Muchart, Francesc Palau, Judith Armstrong, Dèlia Yubero, Carlos Eduardo Valera, Verónica González, Mar O'’Callaghan, Ariadna Borràs, Àngels García-Cazorla, Óscar Casis, Amaia Alquiza, Ainhoa Rodríguez de Yurre, Álvaro Villarroel
Publikováno v:
Pediatric Neurology. 144:11-15
Autor:
Victor Soto Insuga, Luis Gutiérrez Solana, Fernando Ferragut Ferretjans, Anna Duat Rodríguez, Marta Furones García, Verónica Cantarín Extremera, Juan José García Peñas, Maria-Luz Ruiz Falcó, Beatriz Bernardino Cuesta, María Jiménez Legido, Teresa Moreno Cantero, Elena González Alguacil
Publikováno v:
Epilepsy research. 177
Background and objectives To determine the efficacy, tolerance, and safety of BRV in children with epilepsy. Methods A retrospective study of patients with epilepsy who received treatment with BRV before age 16 years and underwent a minimum follow-up
Autor:
Miguel Ángel Fernández-García, Paula Pérez-Albert, Cristina Aparicio López, Teresa de Rojas, Carmen de Lucas Collantes, Luis Gutiérrez-Solana
Publikováno v:
JIMD Reports ISBN: 9783662583647
Mitochondrial diseases (MD) are a heterogeneous group of clinical syndromes characterized by the involvement of different organ systems. They constitute the most prevalent hereditary metabolic disease group.To review the importance of the kidney in M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::016e328156e1b61672c616605b6485a0
https://doi.org/10.1007/8904_2017_78
https://doi.org/10.1007/8904_2017_78
Autor:
Ana Fernández-Marmiesse, Iria Roca, Felícitas Díaz-Flores, Verónica Cantarín, Mª Socorro Pérez-Poyato, Ana Fontalba, Francisco Laranjeira, Sofia Quintans, Oana Moldovan, Blanca Felgueroso, Montserrat Rodríguez-Pedreira, Rogelio Simón, Ana Camacho, Pilar Quijada, Salvador Ibanez-Mico, Mª Rosario Domingno, Carmen Benito, Rocío Calvo, Antonia Pérez-Cejas, Mª Llanos Carrasco, Feliciano Ramos, Mª Luz Couce, Mª Luz Ruiz-Falcó, Luis Gutierrez-Solana, Margarita Martínez-Atienza
Publikováno v:
Frontiers in Neuroscience, Vol 13 (2019)
In order to characterize the genetic architecture of epilepsy in a pediatric population from the Iberian Peninsula (including the Canary Islands), we conducted targeted exome sequencing of 246 patients with infantile-onset seizures with or without ne
Externí odkaz:
https://doaj.org/article/9472500101a14f7eb251f61423ea1fb9