Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Rafaela Caballero-Andaluz"'
Autor:
Rafaela Caballero Andaluz
As the leading partner in the Marco Polo Project, the University of Seville is proud to publish this work. The publication contains essential contributions to the ongoing Higher Education internationalisation debate, but from a new and challenging pe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d86f687d40ab2a6675661b1d6e81af43
https://doi.org/10.12795/9788447229420
https://doi.org/10.12795/9788447229420
Autor:
Eftichia Duketis, Amaia Hervás, Giovanni Malerba, Thomas Bourgeron, Richard Delorme, Barbara Franke, Elisabetta Trabetti, Rafaela Caballero-Andaluz, Marion Benabou, Bru Cormand, Francisco G. Scholl, Christine M. Freitag, Nanda Rommelse, Afsheen Yousaf, Amalia Martinez-Mir, Elena Bacchelli, Agatino Battaglia, Marta Ribasés, Claudio Toma, Bàrbara Torrico, Elena Maestrini, Jan K. Buitelaar, Andreas G. Chiocchetti
Publikováno v:
Autism Research. 10:202-211
Common variants contribute significantly to the genetics of autism spectrum disorder (ASD), although the identification of individual risk polymorphisms remains still elusive due to their small effect sizes and limited sample sizes available for asso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::18c5ca1b178b4bbe7411b09c73a18290
https://doi.org/10.1002/aur.1662
https://doi.org/10.1002/aur.1662
Autor:
Miguel Del Campo, Ivon Cuscó, Josep Antoni Ramos-Quiroga, Ma Inmaculada Planelles, Elisabet Vilella, Yolanda de Diego-Otero, Bàrbara Torrico, Luis A. Pérez-Jurado, A. Hervas, Bru Cormand, Claudio Toma, Marta Salgado, Marta Maristany, Lucía Pérez-Costillas, Rafael Martínez-Leal, Marta Ribasés, Noemí Balmaña, Mònica Bayés, Rafaela Caballero-Andaluz
Publikováno v:
Psychiatric Genetics. 23:82-85
Impairment of language abilities is a common feature in autistic individuals. Heterozygous mutations in the Forkhead Box P2 (FOXP2) gene lead to a severe spoken language disorder. Recently, several studies have pinpointed the involvement of common va
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67b5ad440717ac9206105e6025e5084a
https://doi.org/10.1097/ypg.0b013e32835d6fc6
https://doi.org/10.1097/ypg.0b013e32835d6fc6
Autor:
Guadalupe Guzmán-Alvarez, Yolanda de Diego-Otero, Francisco Aguilera, Josep Antoni Ramos-Quiroga, Bru Cormand, Elisabet Vilella, Luis A. Pérez-Jurado, Fátima Gallastegui, Mònica Bayés, Rafaela Caballero-Andaluz, Amaia Hervás, Marta Salgado, Noemí Balmaña, Claudio Toma, Carmen Orejuela, Marta Maristany, Marta Ribasés, Ivon Cuscó
Publikováno v:
The World Journal of Biological Psychiatry. 14:516-527
Neurotransmitter systems and neurotrophic factors can be considered strong candidates for autism spectrum disorder (ASD). The serotoninergic and dopaminergic systems are involved in neurotransmission, brain maturation and cortical organization, while
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bed6a8b96431d23b9aebf0b50807dab1
https://doi.org/10.3109/15622975.2011.602719
https://doi.org/10.3109/15622975.2011.602719
Autor:
Lourdes Sánchez-Salido, Francisco Garcia-Guirado, Yolanda de Diego-Otero, Ignacio del Arco-Herrera, Rafaela Caballero-Andaluz, Teresa Ferrando-Lucas, Carolina Quintero-Navarro, Isabel Fernandez-Carvajal, Lucía Pérez-Costillas, R. Calvo-Medina
Publikováno v:
Trials
Digital.CSIC. Repositorio Institucional del CSIC
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Digital.CSIC. Repositorio Institucional del CSIC
instname
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0).
[Background]: Fragile X syndrome (FXS) is an inherited neurodevelopmental condition characterise
[Background]: Fragile X syndrome (FXS) is an inherited neurodevelopmental condition characterise
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::940cfa245747909aca12b5b601872c9f
https://pubmed.ncbi.nlm.nih.gov/25187257
https://pubmed.ncbi.nlm.nih.gov/25187257