Zobrazeno 1 - 10
of 201
pro vyhledávání: '"Assumpta Caixàs"'
Autor:
Josep León-Mengíbar, Enric Sánchez, Ferrán Herrerías, Mari Cruz De La Fuente, Maite Santamaría, José Manuel Valdivielso, Marcelino Bermúdez-López, Eva Castro, Judit Pallarés, Xavier Matias-Guiu, Felip Vilardell, Assumpta Caixàs, Marta Bueno, Raquel Martí, Albert Lecube
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
IntroductionNonalcoholic fatty liver disease (NAFLD) affects a quarter of the world’s population and encompasses a spectrum of liver conditions, from non-alcoholic steatohepatitis (NASH) to inflammation and fibrosis. In addition, NAFLD also links t
Externí odkaz:
https://doaj.org/article/eaa2eec326e04ad7b3143538377bfe90
Autor:
Tura Benítez, Assumpta Caixàs, Pere Rebasa, Alexis Luna, Sara Crivillés, Teresa Gutiérrez, Joan Deus
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-9 (2023)
Abstract Presurgical psychopathological assessment usually focuses on detecting severe mental disorders. However, mild intensity psychopathology and eating behaviour pattern may also influence postsurgical outcomes. The aim was to identify psychopath
Externí odkaz:
https://doaj.org/article/0e07e21034284a73b9a8e3eed9f315db
Autor:
Denise H. van Abswoude, Karlijn Pellikaan, Naomi Nguyen, Anna G. W. Rosenberg, Kirsten Davidse, Franciska M. E. Hoekstra, Ilse M. Rood, Christine Poitou, Graziano Grugni, Charlotte Høybye, Tania P. Markovic, Assumpta Caixàs, Antonino Crinò, Sjoerd A. A. van den Berg, Aart J. van der Lely, Laura C. G. de Graaff
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
Externí odkaz:
https://doaj.org/article/4bb7a1911f2d4e0e918bd1cd80546a0c
Genetic testing for familial hyperparathyroidism: clinical-genetic profile in a Mediterranean cohort
Autor:
Isabel Mazarico-Altisent, Ismael Capel, Neus Baena, Maria Rosa Bella-Cueto, Santi Barcons, Xavier Guirao, Rocío Pareja, Andreea Muntean, Valeria Arsentales, Assumpta Caixàs, Mercedes Rigla
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
BackgroundApproximately 10% of primary hyperparathyroidism cases are hereditary, due to germline mutations in certain genes. Although clinically relevant, a systematized genetic diagnosis is missing due to a lack of firm evidence regarding individual
Externí odkaz:
https://doaj.org/article/fd79259ca4f343449091ac1e86afec29
Autor:
Denise H. van Abswoude, Karlijn Pellikaan, Naomi Nguyen, Anna G. W. Rosenberg, Kirsten Davidse, Franciska M. E. Hoekstra, Ilse M. Rood, Christine Poitou, Graziano Grugni, Charlotte Høybye, Tania P. Markovic, Assumpta Caixàs, Antonino Crinò, Sjoerd A. A. van den Berg, Aart J. van der Lely, Laura C. G. de Graaff
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
BackgroundPrader-Willi syndrome (PWS) is a rare, complex, genetic disorder characterized by hyperphagia, hypotonia, delayed psychomotor development, low muscle mass and hypothalamic dysfunction. Adults with PWS often have obesity, hypertension and ty
Externí odkaz:
https://doaj.org/article/b7fe49a89b8d4fd9b087a1e6cebb9573
Autor:
Yolanda Couto-Rosende, Diana Garcia-Tirado, Mónica Palacio-Marco, Assumpta Caixàs, Raquel Corripio
Publikováno v:
Journal of Clinical Medicine, Vol 12, Iss 12, p 3967 (2023)
Prader–Willi Syndrome (PWS) is the most frequent cause of genetic obesity. Early reports indicate that children with PWS require 20–40% fewer calories than healthy children to maintain adequate growth. Growth hormone treatment for children with P
Externí odkaz:
https://doaj.org/article/1a09a8bc79bf4015aaa6a3a4f3799874
Autor:
Lauren Schwartz, Assumpta Caixàs, Anastasia Dimitropoulos, Elisabeth Dykens, Jessica Duis, Stewart Einfeld, Louise Gallagher, Anthony Holland, Lauren Rice, Elizabeth Roof, Parisa Salehi, Theresa Strong, Bonnie Taylor, Kate Woodcock
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 13, Iss 1, Pp 1-13 (2021)
Abstract Prader-Willi syndrome (PWS) is a rare neurodevelopmental genetic disorder associated with a characteristic behavioral phenotype that includes severe hyperphagia and a variety of other behavioral challenges such as temper outbursts and anxiet
Externí odkaz:
https://doaj.org/article/a466c191ad0f4cdc8dfe5ffff5827f66
Autor:
Rocío Escartín, Maria Font, José Miguel González-Clemente, Joan Vendrell, Assumpta Caixàs, Raquel Corripio
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
ObjectiveObesity is characterized by a low-grade inflammatory state in adipose tissue. Tumor Necrosis Factor Weak Inducer of Apoptosis (TWEAK) and Cluster of Differentiation 163 (CD163) are cytokines potentially involved in the pathogenesis of obesit
Externí odkaz:
https://doaj.org/article/1d69e0bc960c4ccfa72b957176b71b36
Autor:
Sara Gámez, Jesus Cobo, Meritxell Fernández-Lafitte, Ramón Coronas, Isabel Parra, Joan Carles Oliva, Aida Àlvarez, Susanna Esteba-Castillo, Olga Giménez-Palop, Raquel Corripio, Diego J. Palao, Assumpta Caixàs
Publikováno v:
Journal of Clinical Medicine, Vol 12, Iss 3, p 1155 (2023)
Prader–Willi syndrome (PWS) is a genetic disorder produced by a lack of expression of paternally derived genes in the 15q11–13 region. Research has generally focused on its genetic and behavioral expression, but only a few studies have examined e
Externí odkaz:
https://doaj.org/article/4454a3673a7c46358b920dc7e1785b8f
Autor:
Jose León Mengíbar, Ismael Capel, Teresa Bonfill, Isabel Mazarico, Laia Casamitjana Espuña, Assumpta Caixàs, Mercedes Rigla
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-4 (2019)
Durvalumab, a human immunoglobulin G1 kappa monoclonal antibody that blocks the interaction of programmed cell death ligand 1 (PD-L1) with the PD-1 and CD80 (B7.1) molecules, is increasingly used in advanced neoplasias. Durvalumab use is associated w
Externí odkaz:
https://doaj.org/article/93f45ffdb87947429811fbe62ca91869