Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Carla Manterola"'
Autor:
Leonie Kausel, Alejandra Figueroa-Vargas, Francisco Zamorano, Ximena Stecher, Mauricio Aspé-Sánchez, Patricio Carvajal-Paredes, Victor Márquez-Rodríguez, María Paz Martínez-Molina, Claudio Román, Patricio Soto-Fernández, Gabriela Valdebenito-Oyarzo, Carla Manterola, Reinaldo Uribe-San-Martín, Claudio Silva, Rodrigo Henríquez-Ch, Francisco Aboitiz, Rafael Polania, Pamela Guevara, Paula Muñoz-Venturelli, Patricia Soto-Icaza, Pablo Billeke
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-14 (2024)
Abstract Patients recovering from COVID-19 commonly exhibit cognitive and brain alterations, yet the specific neuropathological mechanisms and risk factors underlying these alterations remain elusive. Given the significant global incidence of COVID-1
Externí odkaz:
https://doaj.org/article/8e08439f44554f6dafbf261e2474c97e
Autor:
Viviana Venegas, Carla Manterola, Jose De Pablo, Mariano Garcia, Sonia Ponce deLeón, Gabriel Cavada
Publikováno v:
Epilepsia Open, Vol 7, Iss 3, Pp 442-451 (2022)
Abstract Objective This study aimed to describe the characteristics of pediatric neurologists (PNs) in Latin America (LA) who attend to children and adolescents with epilepsy and convey to them the risk of sudden unexpected death in epilepsy (SUDEP).
Externí odkaz:
https://doaj.org/article/addc99bfe54746a09eafbf74a8240779
Autor:
Ximena Stecher, Valeria Schonstedt, Carla Manterola, Fernando Carreño, Francisco Zamorano, Alvaro Velasquez, Mauricio Castillo
Publikováno v:
Epilepsia Open, Vol 6, Iss 1, Pp 235-238 (2021)
Abstract Objective To report our initial experience using an adult‐template MAP in drug‐resistant focal epilepsy in five children with apparently normal MRI. Methods Patients selected were highly suspicious of harboring focal structural lesions a
Externí odkaz:
https://doaj.org/article/52db1e1b58114df7a326a1586588f91f
Autor:
Carla Manterola, Fernando Carreño, Mauricio Castillo, Francisco Zamorano, Alvaro Velasquez, Valeria Schonstedt, Ximena Stecher
Publikováno v:
Epilepsia Open, Vol 6, Iss 1, Pp 235-238 (2021)
Epilepsia Open
Epilepsia Open
Objective To report our initial experience using an adult‐template MAP in drug‐resistant focal epilepsy in five children with apparently normal MRI. Methods Patients selected were highly suspicious of harboring focal structural lesions and had ne
Autor:
Camila Cortes, Carla Manterola
Publikováno v:
Epilepsybehavior : EB. 112
Levetiracetam (LEV) has an improved pharmacological profile and is one of the most commonly used antiepileptic drugs (AEDs). However, associations between this pharmacological profile and behavioral side effects have been extensively reported in pedi
Publikováno v:
Revista chilena de pediatría v.91 n.1 2020
SciELO Chile
CONICYT Chile
instacron:CONICYT
SciELO Chile
CONICYT Chile
instacron:CONICYT
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5f91f2d18b4e92f61104c1fe2b68142
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0370-41062020000100007
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0370-41062020000100007
Autor:
Karla L Loss, Carla Manterola, Alberto Farina, Osama E A Idris, Anna Stein, Pierina Danos, Elias M Morón, Carolina F de Sousa, Dina Maki, Antônio Felipe Raquelo-Menegassio, Rofida A A Mahmoud, Carolina Victor, Rocio Ortiz-Lopez, Sergio Gresse, Fabiano Ferreira Abrantes, Fatima Iqbal, Lorenzo Thompson, Joanna Jimenez-Pavón, Mariam W J Nashwan, Anthony Gutierrez, Jazmin Camacho-Vilchez, Matthias Diebold, Lygia Bonanato, Marianna A G Galvani, Daniella Braz Parente, Erica V Stelmaszewski, Maria V C P Da Silva, Juan P Polania
Publikováno v:
Cardiology in the young. 30(3)
Introduction:Tuberous sclerosis complex is a rare genetic disorder leading to the growth of hamartomas in multiple organs, including cardiac rhabdomyomas. Children with symptomatic cardiac rhabdomyoma require frequent admissions to intensive care uni
Publikováno v:
Revista Chilena de Pediatría. 91:260
La deficiencia del transportador de glucosa tipo 1 constituye un síndrome (SD-GLUT1), provocado por la mutación del gen SLC2A1, que codifica la proteína transportadora de glucosa al encéfalo. Las manifestaciones neurológicas se dan en tres domin
Autor:
Felipe, Quezada, Richard, Castillo, Constanza, Villalón, José Miguel, Zúñiga, Carla, Manterola, María Elena, Molina, Felipe, Bellolio, Gonzalo, Urrejola
Publikováno v:
Revista medica de Chile. 143(5)
A loop ileostomy with intraoperative anterograde colonic lavage has been described as an alternative to colectomy in the management of cases of Clostridium difficile infection refractory to medical treatment. We report a 69 years old diabetic women a