Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Yolanda, de Diego"'
Autor:
Ana Aragón-González, Allan C Shaw, Jannigje R Kok, Florence S Roussel, Cleide dos Santos Souza, Sarah M Granger, Tatyana Vetter, Yolanda de Diego, Kathrin C Meyer, Selina N Beal, Pamela J Shaw, Laura Ferraiuolo
Publikováno v:
Fluids and Barriers of the CNS, Vol 21, Iss 1, Pp 1-14 (2024)
Abstract The blood-brain barrier (BBB) serves as a highly intricate and dynamic interface connecting the brain and the bloodstream, playing a vital role in maintaining brain homeostasis. BBB dysfunction has been associated with multiple neurodegenera
Externí odkaz:
https://doaj.org/article/3b68b76102ee4ab192145d471b0955af
Autor:
Jose Guzman-Parra, Fabian Streit, Andreas J. Forstner, Jana Strohmaier, Maria José González, Susana Gil Flores, Francisco J. Cabaleiro Fabeiro, Francisco del Río Noriega, Fermin Perez Perez, Jesus Haro González, Guillermo Orozco Diaz, Yolanda de Diego-Otero, Berta Moreno-Kustner, Georg Auburger, Franziska Degenhardt, Stefanie Heilmann-Heimbach, Stefan Herms, Per Hoffmann, Josef Frank, Jerome C. Foo, Lea Sirignano, Stephanie H. Witt, Sven Cichon, Fabio Rivas, Fermín Mayoral, Markus M. Nöthen, Till F. M. Andlauer, Marcella Rietschel
Publikováno v:
Translational Psychiatry, Vol 11, Iss 1, Pp 1-10 (2021)
Abstract The two major subtypes of bipolar disorder (BD), BD-I and BD-II, are distinguished based on the presence of manic or hypomanic episodes. Historically, BD-II was perceived as a less severe form of BD-I. Recent research has challenged this con
Externí odkaz:
https://doaj.org/article/bbfe0516372846358808b84f40df1628
Autor:
Elena Díaz-Santiago, M. Gonzalo Claros, Raquel Yahyaoui, Yolanda de Diego-Otero, Rocío Calvo, Janet Hoenicka, Francesc Palau, Juan A. G. Ranea, James R. Perkins
Publikováno v:
Frontiers in Molecular Biosciences, Vol 8 (2021)
Neuromuscular disorders (NMDs) represent an important subset of rare diseases associated with elevated morbidity and mortality whose diagnosis can take years. Here we present a novel approach using systems biology to produce functionally-coherent phe
Externí odkaz:
https://doaj.org/article/0b1a57da523a479ebbf16cd47b3994b9
Autor:
Jose Guzman-Parra, Nicolás Sánchez-Álvarez, Justyna Guzik, Trinidad Bergero-Miguel, Yolanda de Diego-Otero, Lucía Pérez-Costillas
Publikováno v:
Archives of Sexual Behavior.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b1619eccec326311ba670224f4c0da3
https://doi.org/10.1007/s10508-023-02594-7
https://doi.org/10.1007/s10508-023-02594-7
Publikováno v:
Children, Vol 8, Iss 2, p 164 (2021)
Due to the exponential increase of autism spectrum disorders’ prevalence in Western countries, it is necessary to improve early detection and intervention to enhance developmental milestones. This systematic review identified the most effective scr
Externí odkaz:
https://doaj.org/article/cd098def4ae54e95bdd8ffab372eb55c
Autor:
Noora Putkonen, Asta Laiho, Doug Ethell, Juha Pursiheimo, Anna-Kaisa Anttonen, Juho Pitkonen, Adriana M. Gentile, Yolanda de Diego-Otero, Maija L. Castrén
Publikováno v:
Cells, Vol 9, Iss 2, p 289 (2020)
A triplet repeat expansion leading to transcriptional silencing of the FMR1 gene results in fragile X syndrome (FXS), which is a common cause of inherited intellectual disability and autism. Phenotypic variation requires personalized treatment approa
Externí odkaz:
https://doaj.org/article/1c9531baa28f4443aa9700608cccba12
Autor:
Yolanda de Diego Otero, Lucía Pérez Costillas, Rocío Calvo Medina, Carolina Quintero Navarro, Isabel del Pino Benítez, Yolanda Casado Martín, Cristina Nogueira Cobas
Publikováno v:
Revista Española de Discapacidad, Vol 5, Iss 1 (2017)
De Diego Otero, Y. et al. (2017): “Avances en investigación de la discapacidad intelectual de origen genético: tratamientos experimentales en el síndrome X frágil”. Revista Española de Discapacidad, 5 (I): 217-227.
Externí odkaz:
https://doaj.org/article/e3ecda9bafc141fc828de9d32c78017a
Autor:
Yolanda de Diego, Abdelkrim Hmadcha, Francisco Moron, Miguel Lucas, Mercedes Carrasco, Elizabeth Pintado
Publikováno v:
Genetics and Molecular Biology, Vol 25, Iss 1, Pp 01-06 (2002)
Fragile X syndrome is the most common inherited form of mental retardation. We investigated the prevalence of the Fragile X syndrome in the population with mental retardation of unknown etiology in Andalusia, South Spain. We analyzed 322 unrelated pa
Externí odkaz:
https://doaj.org/article/0fa4dd4fee694c2dacc8022f76e9a674
Autor:
Juho Pitkonen, Asta Laiho, Noora Putkonen, Anna-Kaisa Anttonen, Adriana Gentile, Maija L. Castrén, Juha-Pekka Pursiheimo, Doug Ethell, Yolanda de Diego-Otero
Publikováno v:
Cells
Volume 9
Issue 2
Cells, Vol 9, Iss 2, p 289 (2020)
Volume 9
Issue 2
Cells, Vol 9, Iss 2, p 289 (2020)
A triplet repeat expansion leading to transcriptional silencing of the FMR1 gene results in fragile X syndrome (FXS), which is a common cause of inherited intellectual disability and autism. Phenotypic variation requires personalized treatment approa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cddcb0888607d9127feaea578c4c1411
Publikováno v:
Medicina Clínica. 152:307-309
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b0a9d4310800e817063918bc075483a
https://doi.org/10.1016/j.medcli.2018.11.023
https://doi.org/10.1016/j.medcli.2018.11.023