Zobrazeno 1 - 10
of 75
pro vyhledávání: '"Juan José García Peñas"'
Autor:
Jana Ruiz Herrero, Elvira Cañedo Villarroya, Juan José García Peñas, Beatriz García Alcolea, Begoña Gómez Fernández, Laura Andrea Puerta Macfarland, Consuelo Pedrón-Giner
Publikováno v:
Anales de Pediatría (English Edition), Vol 96, Iss 6, Pp 511-522 (2022)
Aim: Ketogenic dietary therapies (KDT) produce anticonvulsant and neuroprotective effects, reduce seizures and improve the cognitive state in patients with epilepsy. Our purpose was to evaluate the effects of KDT in children with refractory epilepsy
Externí odkaz:
https://doaj.org/article/6faac18bb2524af28bd08e23eb22d040
Autor:
Jana Ruiz Herrero, Elvira Cañedo Villarroya, Juan José García Peñas, Beatriz García Alcolea, Begoña Gómez Fernández, Laura Andrea Puerta Macfarland, Consuelo Pedrón-Giner
Publikováno v:
Anales de Pediatría, Vol 96, Iss 6, Pp 511-522 (2022)
Resumen: Introducción: Las terapias dietéticas cetogénicas (TDC) tienen efecto neuroprotector y anticonvulsivante, reducen las crisis epilépticas y mejoran el estado cognitivo en pacientes epilépticos. Nuestro propósito fue evaluar los efectos
Externí odkaz:
https://doaj.org/article/31e95c6d50a54c93b7e1c0383ead2e98
Autor:
Anna Duat Rodríguez, Verónica Cantarín Extremera, Marta García Fernández, Juan José García Peñas, María Luz Ruiz-Falcó Rojas
Publikováno v:
Anales de Pediatría, Vol 91, Iss 5, Pp 346-348 (2019)
Externí odkaz:
https://doaj.org/article/8f2adafe3bde466a977be9361643dd6e
Autor:
Anna Duat Rodríguez, Verónica Cantarín Extremera, Marta García Fernández, Juan José García Peñas, María Luz Ruiz-Falcó Rojas
Publikováno v:
Anales de Pediatría (English Edition), Vol 91, Iss 5, Pp 346-348 (2019)
Externí odkaz:
https://doaj.org/article/59ff589d78064bcaa02840ca86da8d50
Autor:
Jana Ruiz Herrero, Elvira Cañedo Villarroya, Juan José García Peñas, Beatriz García Alcolea, Begoña Gómez Fernández, Laura Andrea Puerta Macfarland, Consuelo Pedrón Giner
Publikováno v:
Nutrients, Vol 12, Iss 2, p 306 (2020)
Background: The ketogenic diet (KD) is an effective treatment against drug-resistant epilepsy in children. The KD is a diet rich in fats that produces anticonvulsant and neuroprotective effects that reduces seizures and improves the cognitive state.
Externí odkaz:
https://doaj.org/article/8f0e51c503af42f489af21769c8e4d05
Autor:
Begoña Gómez Fernández, Elvira Cañedo Villarroya, Laura Andrea Puerta Macfarland, C. Pedrón-Giner, Beatriz García Alcolea, Jana Ruiz Herrero, Juan José García Peñas
Publikováno v:
Anales de Pediatría. 96:511-522
Resumen Introduccion Las terapias dieteticas cetogenicas (TDC) tienen efecto neuroprotector y anticonvulsivante, reducen las crisis epilepticas y mejoran el estado cognitivo en pacientes epilepticos. Nuestro proposito fue evaluar los efectos de las T
Autor:
Vicente Villanueva, Adrián García-Ron, Patricia Smeyers, Eva Arias, Victor Soto, Juan José García-Peñas, Elena González-Alguacil, Débora Sayas, Pedro Serrano-Castro, Mercedes Garces, Kevin Hampel, Miguel Tomás, Julian Lara, María de Toledo, Ines Barceló, Angel Aledo-Serrano, Antonio Gil-Nagel, Lucas Iacampo, Mercè Falip, Rosa Ana Saiz-Diaz, Asier Gómez-Ibañez, David Sopelana, Alvaro Sanchez-Larsen, Francisco Javier López-González
Publikováno v:
Epilepsybehavior : EB. 137
To evaluate the effectiveness and tolerability of cannabidiol (CBD) in patients with developmental and epileptic encephalopathies, including Dravet syndrome (DS), and Lennox-Gastaut syndrome (LGS), in a Spanish Expanded Access Program (EAP).This was
Autor:
María Jiménez Legido, Anna Duat Rodríguez, Nelmar Valentina Ortiz Cabrera, Juan José García Peñas, Verónica Cantarín Extremera, Bárbara Fernández Garoz, Beatriz Bernardino Cuesta
Publikováno v:
Molecular Syndromology. 12:25-32
Epileptic encephalopathy related to CACNA1E has been described as a severe neurodevelopmental disorder presenting with early-onset refractory seizures, hypotonia, macrocephaly, hyperkinetic movements, and contractures and is associated with an autoso
Autor:
Juan José García-Peñas, Álvaro Martín-Rivada, Laura María Palomino Pérez, C. Pedrón-Giner, Elvira Cañedo Villaroya, Margarita Cuervas-Mons Vendrell
Publikováno v:
JIMD Reports, Vol 55, Iss 1, Pp 3-11 (2020)
JIMD Reports
JIMD Reports
Hyperammonemic encephalopathy is a rare but potentially dangerous complication of the antiepileptic drug (AED) sodium valproate (VPA). We report a retrospective study of 25 pediatric patients, (15 females [60%]; age: 7.6 ± 4.9 years), with different
Autor:
Alberto García-Salido, María Luz Ruiz-Falcó-Rojas, Juan José García-Peñas, Inés Solís-Muñiz, Verónica Cantarín-Extremera, Beatriz Bernardino-Cuesta, María Jiménez-Legido, Víctor Soto-Insuga, Anna Duat-Rodríguez, Amelia Martínez-de-Azagra-Garde
Publikováno v:
European Journal of Paediatric Neurology. 27:60-66
Introduction Sturge-Weber syndrome (SWS) is a neurocutaneous syndrome with typical clinical features including seizures, chronic hemiplegia, hemianopsia and intellectual impairment. Progressive clinical decline may be attributable, at least in part,