Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Miquel, Tuson"'
Autor:
Víctor Pérez, Ariana Salavert, Jordi Espadaler, Miquel Tuson, Jerónimo Saiz-Ruiz, Cristina Sáez-Navarro, Julio Bobes, Enrique Baca-García, Eduard Vieta, José M. Olivares, Roberto Rodriguez-Jimenez, José M. Villagrán, Josep Gascón, Josep Cañete-Crespillo, Montse Solé, Pilar A. Saiz, Ángela Ibáñez, Javier de Diego-Adeliño, AB-GEN Collaborative Group, José M. Menchón
Publikováno v:
BMC Psychiatry, Vol 17, Iss 1, Pp 1-13 (2017)
Abstract Background A 12-week, double-blind, parallel, multi-center randomized controlled trial in 316 adult patients with major depressive disorder (MDD) was conducted to evaluate the effectiveness of pharmacogenetic (PGx) testing for drug therapy g
Externí odkaz:
https://doaj.org/article/d5844f200b4f4f299135845fb3c486c5
Publikováno v:
Pharmaceutics, Vol 11, Iss 9, p 453 (2019)
Several pharmacogenetic tests to support drug selection in psychiatric patients have recently become available. The current meta-analysis aimed to assess the clinical utility of a commercial pharmacogenetic-based tool for psychiatry (Neuropharmagen®
Externí odkaz:
https://doaj.org/article/bfc32c840b584a38994b831d125692ef
Autor:
Cristina Villanueva-Mendoza, David Apam-Garduño, Jean Remi Trotta, Vianney Cortés-González, Gemma Marfany, Rebeca Valero, Miquel Tuson, Raul Tonda, Marta de Castro-Miró, Roser Gonzàlez-Duarte
Publikováno v:
Genes, Vol 12, Iss 1824, p 1824 (2021)
Dipòsit Digital de la UB
Universidad de Barcelona
Genes
Volume 12
Issue 11
Dipòsit Digital de la UB
Universidad de Barcelona
Genes
Volume 12
Issue 11
In this work, we aimed to provide the genetic diagnosis of a large cohort of patients affected with inherited retinal dystrophies (IRDs) from Mexico. Our data add valuable information to the genetic portrait in rare ocular diseases of Mesoamerican po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c623eeab64ab4485ae3531125b2437c
http://hdl.handle.net/2445/184072
http://hdl.handle.net/2445/184072
Autor:
Jordi Espadaler-Mazo, Eva Solé, Gerard Anmella, Mercè Brat, Isabella Pacchiarotti, Andrea Murru, Miquel Tuson, Silvia Vilches, Giovanna Fico, Marina Garriga, Eduard Vieta
Publikováno v:
Genes
Volume 12
Issue 8
Genes, Vol 12, Iss 1259, p 1259 (2021)
Volume 12
Issue 8
Genes, Vol 12, Iss 1259, p 1259 (2021)
Several pharmacogenetic-based decision support tools for psychoactive medication selection are available. However, the scientific evidence of the gene-drug pairs analyzed is mainly based on pharmacogenetic studies in patients with major depression or
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6d3f4f3f9fa4a08c2b2b3b29f0dcc19
http://europepmc.org/articles/PMC8391230
http://europepmc.org/articles/PMC8391230
Autor:
Roser, Gonzàlez-Duarte, Marta, de Castro-Miró, Miquel, Tuson, Valeria, Ramírez-Castañeda, Rebeca Valero, Gils, Gemma, Marfany
Publikováno v:
Advances in experimental medicine and biology. 1185
During the last 20 years, our group has focused on identifying the genes and mutations causative of inherited retinal dystrophies (IRDs). By applying massive sequencing approaches (NGS) in more than 500 familial and sporadic cases, we attained high d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ca582e8f09db1e71325a61be9896967c
https://pubmed.ncbi.nlm.nih.gov/31884614
https://pubmed.ncbi.nlm.nih.gov/31884614
Autor:
Miquel Tuson, Eduard Vieta, Virgili Pérez, Jerónimo Saiz-Ruiz, Jordi Espadaler, Julio Bobes, Enric Álvarez, José M. Menchón
Publikováno v:
Journal of Neural Transmission. 126:95-99
Clinical utility of commercial multi-gene pharmacogenetic tests in depression is starting to be studied with some promising results on efficacy and tolerability. Among the next steps is the definition of the patient profile that is most likely to ben
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4129b7c1a1292c0ad5769c06a46f8b52
https://doi.org/10.1007/s00702-018-1879-z
https://doi.org/10.1007/s00702-018-1879-z
Publikováno v:
PLoS ONE, Vol 4, Iss 8, p e6839 (2009)
Sonic hedgehog (Shh) signaling in the mouse requires the microtubule-based organelle, the primary cilium. The primary cilium is assembled and maintained through the process of intraflagellar transport (IFT) and the response to Shh is blocked in mouse
Externí odkaz:
https://doaj.org/article/4fb23349225b446fbf241da89510dcf8
Autor:
Miquel Tuson, Rebeca Valero Gils, Marta de Castro-Miró, Valeria Ramírez-Castañeda, Roser Gonzàlez-Duarte, Gemma Marfany
Publikováno v:
Retinal Degenerative Diseases ISBN: 9783030273774
During the last 20 years, our group has focused on identifying the genes and mutations causative of inherited retinal dystrophies (IRDs). By applying massive sequencing approaches (NGS) in more than 500 familial and sporadic cases, we attained high d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f79b0c529174d16349e6caf3974bedf
https://doi.org/10.1007/978-3-030-27378-1_35
https://doi.org/10.1007/978-3-030-27378-1_35
Autor:
María I López-Ibor, Jose Miguel Lopez-Ibor, Franciso Lopez-Ibor, Miquel Tuson, Jordi Espadaler
Publikováno v:
CNS Spectrums. 22:315-324
ObjectiveWe investigated the association between clinical outcome and the recommendations of a pharmacogenetic test (Neuropharmagen) in patients with a variety of psychiatric conditions whose previous treatment regimen had failed.MethodsThis retrospe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::663d44f85bf9762871eae8e729e3eaf7
https://doi.org/10.1017/s1092852915000711
https://doi.org/10.1017/s1092852915000711
Autor:
Juan Miguel Garrido Ocaña, Javier Quintero, JOSE CAÑETE, ANGELA IBAÑEZ, Miquel Tuson, Javier De Diego-Adeliño, Virginia Soria, Victor Perez, Jose Menchon, Jordi Espadaler Mazo, Diego Palao, Marta Puigmulé, Pilar A. Saiz, Enrique Baca-García, Marina Garriga, Maria Luisa Barrigon, Jose Villagran, Paz Garcia-Portilla, Julio Bobes, Roberto Sánchez-González, Fermin Mayoral-Cleries, Miquel Bernardo, Eva Aguilar, Gemma Safont, Eduard Vieta, Jose M Olivares
Publikováno v:
Recercat. Dipósit de la Recerca de Catalunya
instname
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Biblos-e Archivo. Repositorio Institucional de la UAM
Scopus
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
BMC Psychiatry
RUO. Repositorio Institucional de la Universidad de Oviedo
Dipòsit Digital de la UB
Universidad de Barcelona
BMC Psychiatry, Vol 17, Iss 1, Pp 1-13 (2017)
instname
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Biblos-e Archivo. Repositorio Institucional de la UAM
Scopus
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
BMC Psychiatry
RUO. Repositorio Institucional de la Universidad de Oviedo
Dipòsit Digital de la UB
Universidad de Barcelona
BMC Psychiatry, Vol 17, Iss 1, Pp 1-13 (2017)
Background: A 12-week, double-blind, parallel, multi-center randomized controlled trial in 316 adult patients with major depressive disorder (MDD) was conducted to evaluate the effectiveness of pharmacogenetic (PGx) testing for drug therapy guidance.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57ae26ca80555d358d82e1f90ec2d001
http://hdl.handle.net/10230/34398
http://hdl.handle.net/10230/34398