Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Alba Valiente-Pallejà"'
Autor:
Yolanda Alonso, Carmen Miralles, M. José Algora, Alba Valiente-Pallejà, Vanessa Sánchez-Gistau, Gerard Muntané, Javier Labad, Elisabet Vilella, Lourdes Martorell
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-11 (2022)
Abstract Metabolic syndrome (MetS) is a cluster of parameters encompassing the most dangerous heart attack risk factors, associated with increased morbidity and mortality. It is highly prevalent in recent-onset psychosis (ROP) patients. In this pilot
Externí odkaz:
https://doaj.org/article/86a0446c2007477d8bd603b6fe0fdbe9
Autor:
Alba Valiente-Pallejà, Juan Tortajada, Bengisu K. Bulduk, Elisabet Vilella, Glòria Garrabou, Gerard Muntané, Lourdes Martorell
Publikováno v:
EBioMedicine, Vol 76, Iss , Pp 103815- (2022)
Summary: Background: Mitochondrial DNA (mtDNA) encodes 37 genes necessary for synthesizing 13 essential subunits of the oxidative phosphorylation system. mtDNA alterations are known to cause mitochondrial disease (MitD), a clinically heterogeneous gr
Externí odkaz:
https://doaj.org/article/fa7cb403b94e4d329a0710948ccd3fce
Autor:
Helena Torrell, Juan Tortajada Valero, Elisabet Vilella, Bengisu Bulduk, Leire Torres-Egurrola, Gerard Muntané, Lourdes Martorell, Alba Valiente-Pallejà
Publikováno v:
European Neuropsychopharmacology. 51:e126-e127
Autor:
Juan Tortajada Valero, Alba Valiente-Pallejà, Elisabet Vilella, Bengisu Bulduk, Lourdes Martorell, Gerard Muntané
Publikováno v:
European Neuropsychopharmacology. 51:e236-e237
Publikováno v:
Acta neuropsychiatrica. 32(5)
Objective:It has been hypothesised that neuropsychiatric symptoms, including psychosis, can be the result of a milder brain bioenergetic defect produced by mitochondrial dysfunction; however, mitochondrial dysfunction can be present in other organs o
Autor:
Elisabet Vilella, Helena Torrell, Yolanda Alonso, Gerard Muntané, Alba Valiente-Pallejà, Lourdes Martorell
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
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Background: Mitochondrial dysfunction and an elevation of lactate are observed in patients with schizophrenia (SZ). However, it is unknown whether mitochondrial dysfunction is associated with the presence of mitochondrial DNA (mtDNA) alterations and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c80c9c34d3fd7b7e5613341bb636267
http://hdl.handle.net/10261/236731
http://hdl.handle.net/10261/236731
Autor:
Helena Torrell, Elisabet Vilella, Gerard Muntané, Lourdes Martorell, Nerea Abasolo, Alba Valiente-Pallejà, Rafael Martínez-Leal, Maria José Cortés, Yolanda Alonso
Publikováno v:
Human molecular genetics. 27(5)
Clinical conditions commonly associated with mitochondrial disorders (CAMDs) are often present in autism spectrum disorders (ASD) and intellectual disability (ID). Therefore, the mitochondrial dysfunction hypothesis has been proposed as a transversal