Información del autor
Autor Lopera, Francisco |
Documentos disponibles escritos por este autor (5)
Añadir el resultado a su cesta Hacer una sugerencia Refinar búsqueda
texto impreso
Language as a superior function, result of the process of phylogenetic evolution, has been studied since long time ago by different disciplines such as philosophy and psychology. However, nowadays thanks to the advance of the neurosciences, the [...]texto impreso
Velez-Pardo, Carlos ; Lorenzo-Betancor, Oswaldo ; Jimenez-Del-Rio, Marlene ; Moreno, Sonia ; Lopera, Francisco ; Cornejo-Olivas, Mario ; Torres, Luis ; Inca-Martinez, Miguel ; Mazzetti, Pilar ; Cosentino, Carlos ; Yearout, Dora ; Waldherr, Sarah M. ; Zabetian, Cyrus P. ; Mata, Ignacio F. | Elsevier | 2019-12-06T20:57:50ZBACKGROUND: Mutations in the glucocerebrosidase (GBA) gene are an important risk factor for Parkinson's disease (PD). However, most GBA genetic studies in PD have been performed in patients of European origin and very few data are available in [...]texto impreso
Velez-Pardo, Carlos ; Lorenzo-Betancor, Oswaldo ; Jimenez-Del-Rio, Marlene ; Moreno, Sonia ; Lopera, Francisco ; Cornejo-Olivas, Mario ; Torres, Luis ; Inca-Martinez, Miguel ; Mazzetti, Pilar ; Cosentino, Carlos ; Yearout, Dora ; Waldherr, Sarah M. ; Zabetian, Cyrus P. ; Mata, Ignacio F. | Elsevier | 2019-07-04T17:01:21ZBackground: Mutations in the glucocerebrosidase (GBA) gene are an important risk factor for Parkinson's disease (PD). However, most GBA genetic studies in PD have been performed in patients of European origin and very few data are available in o[...]texto impreso
Arias P., William H. ; Rojas, Winston ; Moreno, Sonia ; Lopera, Francisco ; Ruiz-Linares, Andrés ; Bedoya, Gabriel | Instituto Colombiano de Antropología e Historia - ICANH | 2012-06-30In a large family from Peque population (Antioquia), there have been found some individuals affected with juvenile Parkinson’s disease, due to the G736A mutation located in exon 6 of the PARK2 gene. As a result of the tri-ethnic composition of o[...]texto impreso
Cornejo-Olivas, Mario ; Torres, Luis ; Velit-Salazar, Mario R. ; Inca-Martinez, Miguel ; Mazzetti, Pilar ; Cosentino, Carlos ; Micheli, Federico ; Perandones, Claudia ; Dieguez, Elena ; Raggio, Victor ; Tumas, Vitor ; Borges, Vanderci ; Ferraz, Henrique B. ; Rieder, Carlos R. M. ; Shumacher-Schuh, Artur ; Velez-Pardo, Carlos ; Jimenez-Del-Rio, Marlene ; Lopera, Francisco ; Chang-Castello, Jorge ; Andreé-Munoz, Brennie ; Waldherr, Sarah ; Yearout, Dora ; Zabetian, Cyrus P. ; Mata, Ignacio F. | Nature Research | 2019-01-25T16:20:56ZMutations in Leucine-Rich Repeat Kinase 2 (LRRK2), primarily located in codons G2019 and R1441, represent the most common genetic cause of Parkinson's disease in European-derived populations. However, little is known about the frequency of these[...]