Zobrazeno 1 - 10
of 83
pro vyhledávání: '"Alberto Velez Van Meerbeke"'
Publikováno v:
Computational and Structural Biotechnology Journal, Vol 20, Iss , Pp 6041-6054 (2022)
Introduction: The development of vaccines against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in record time to cope with the ongoing coronavirus disease 2019 (COVID-19) pandemic has led to uncertainty about their use and the appeara
Externí odkaz:
https://doaj.org/article/ebed5169fc4046d497a28efb0658ae09
Autor:
Diego Alejandro Rodriguez-Gomez, Danna Paola Garcia-Guaqueta, Jesús David Charry-Sánchez, Elias Sarquis-Buitrago, Mariana Blanco, Alberto Velez-van-Meerbeke, Claudia Talero-Gutiérrez
Publikováno v:
BMC Neuroscience, Vol 22, Iss 1, Pp 1-12 (2021)
Abstract Background Autism spectrum disorder (ASD) is a complex neurodevelopmental condition characterized by persistent deficits in social communication and interaction. Common genetic variation appears to play a key role in the development of this
Externí odkaz:
https://doaj.org/article/e0386564e75c4862bf6f2cd5b9246633
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 79, Iss 4, Pp 343-345 (2021)
ABSTRACT Gaius Julius Caesar Augustus Germanicus, better known as Caligula, (12 CE to 41 CE) was the third Roman emperor and ruled only four years. Throughout his life he experienced several traumatic events, and, in addition, historians mention some
Externí odkaz:
https://doaj.org/article/59a69589dd594780b1f8f712da10b5ef
Autor:
Jesús Rodriguez-Quintana, Silvia Bueno-Florez, Laura Mora-Muñoz, Eduardo Orrego-González, Ana M. Barragan, Fabio Suárez-Burgos, Alberto Velez-Van-Meerbeke, Fernando Cendes
Publikováno v:
Seizure. 105:43-51
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a28809354a4aa733ada21b41ffcb377
https://doi.org/10.1016/j.seizure.2022.12.003
https://doi.org/10.1016/j.seizure.2022.12.003
Autor:
Julián Manrique-Niño, Andrés Díaz-Forero, Alberto Velez-van Meerbeke, Sofía Ramírez-Guerrero, Gabriela Florez-Esparza, Claudia Talero-Gutiérrez
Publikováno v:
Heliyon, Vol 6, Iss 11, Pp e05585- (2020)
The study aim was to characterize executive function in 114 children with Down syndrome from a reference institution in Bogotá, Colombia. Children were screened with the Battelle Developmental Inventory to establish their developmental age. Eighty c
Externí odkaz:
https://doaj.org/article/68a981403d86441db5c03aaa14487c6e
Autor:
Carlos Alberto Calderon-Ospina, Jubby Marcela Galvez, Claudia López-Cabra, Natalia Morales, Carlos Martín Restrepo, Jesús Rodríguez, Fabio Ancízar Aristizábal-Gutiérrez, Alberto Velez-van-Meerbeke, Paul Laissue, Dora Janeth Fonseca-Mendoza
Publikováno v:
Frontiers in Pharmacology, Vol 11 (2020)
BackgroundEpilepsy is a serious health problem worldwide. Despite the introduction of new antiepileptic drugs (AEDs) almost 30% of these patients have drug-resistant forms of the disease (DRE), with a significant increase in morbi-mortality.Objective
Externí odkaz:
https://doaj.org/article/9f3719a2c3e144a8b76d410583e31f63
Autor:
Laura Mora-Muñoz, Alejandro Guerrero-Naranjo, Elisa Angélica Rodríguez-Jimenez, Claudio Alberto Mastronardi, Alberto Velez-van-Meerbeke
Publikováno v:
BMC Neuroscience, Vol 19, Iss 1, Pp 1-9 (2018)
Abstract Adipose tissue is a dynamic organ with different effects on the body. Many of these effects are mediated by leptin, a hormone strongly involved in regulation of feeding and energy metabolism. It has an important role as a mediator of neurona
Externí odkaz:
https://doaj.org/article/6d964bca554441cd98ee0a1823ba1a99
Publikováno v:
Acta Neurológica Colombiana, Vol 34, Iss 3 (2018)
OBJETIVO: Revisar la fisiopatología de las craneosinostosis y las deformidades posicionales del cráneo y analizar los tipos de tratamiento, especialmente las ortesis de moldeamiento craneal. MÉTODOS: Revisión de la literatura de e
Externí odkaz:
https://doaj.org/article/a3ddbf6c6b444649b1b4e9dcaa7c1fe7
Autor:
Martha Milade Torres Nupan, Alberto Velez Van Meerbeke, Claudia Alejandra López Cabra, Paula Marcela Herrera Gomez
Publikováno v:
Frontiers in Pediatrics, Vol 5 (2017)
AimThe last systematic review of research on the behavior of children with neurofibromatosis type 1 (NF1) was in 2012. Since then, several important findings have been published. Therefore, the study aim was to synthesize recent relevant work related
Externí odkaz:
https://doaj.org/article/b1fd216932f943b59c903fb4ab8475b6
Publikováno v:
Molecular Syndromology. 12:57-64
Noonan syndrome with multiple lentigines (NSML), previously known as LEOPARD syndrome, is a rare autosomal dominant disorder with an unknown prevalence. Characteristics of this disease include cutaneous, neurologic, and cardiologic abnormalities. In
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f5ced9a3eeec55750b37afc278ecbdd4
https://doi.org/10.1159/000512374
https://doi.org/10.1159/000512374