Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Inés, Losada López"'
Autor:
Lucía Galán Dávila, Fernando Martinez Valle, Juan Buades Reinés, Juan Gonzalez-Moreno, Inés Losada López, Teresa Sevilla, Francisco Muñoz Beamud, José Eulalio Bárcena Llona, Manuel Romero Acebal, Francesca Setaro, Diana Primiano, Patricia Tarilonte
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-10 (2024)
Abstract Background Variant transthyretin amyloidosis (ATTRv) is a rare multisystemic disorder caused by mutations in the transthyretin (TTR) gene. The aim of the present work was to describe the clinical profile of asymptomatic carriers (AC) and Cou
Externí odkaz:
https://doaj.org/article/7af854a35a024965ae84da2f60cdfa1e
Autor:
Juan González-Moreno, Álvaro Gragera-Martínez, Adrián Rodríguez, Cristina Borrachero-Garro, Sandra García-Garrido, Carles Barceló, Ana Manovel-Sánchez, Maria Antonia Ribot-Sansó, Lesly Ibargüen-González, Rosa Gomila, Francisco Muñoz-Beamud, Inés Losada-López, Eugenia Cisneros-Barroso
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-8 (2024)
Abstract Early identification of ATTRv amyloidosis disease onset is still often delayed due to the lack of validated biomarkers of this disease. Light chain neurofilament (NfL) have shown promising results in early diagnosis in this disease, but data
Externí odkaz:
https://doaj.org/article/f491e56deaff4e268c5c6c466f3a8c66
Autor:
Aina Gayà-Barroso, Juan González-Moreno, Adrián Rodríguez, Tomás Ripoll-Vera, Inés Losada-López, Margarita Gili, Milena Paneque, Sara Pérez-Martínez, Eugenia Cisneros-Barroso
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-8 (2023)
Abstract Background Hereditary transthyretin amyloidosis (ATTRv) is a rare genetic disease that negatively affects patients' quality of life through the involvement of various organs and tissues. Despite a large amount of research on medical and psyc
Externí odkaz:
https://doaj.org/article/7ecaeaeaa59e4f45be8fb91e15e07268
Val50Met hereditary transthyretin amyloidosis: not just a medical problem, but a psychosocial burden
Autor:
Juan González-Moreno, Aina Gaya-Barroso, Inés Losada-López, Adrián Rodríguez, Teresa Bosch-Rovira, Tomás Ripoll-Vera, Mercedes Usón, Antoni Figuerola, Cristina Descals, Carles Montalà, María Asunción Ferrer-Nadal, Eugenia Cisneros-Barroso
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-7 (2021)
Abstract Background Hereditary transthyretin (TTR) amyloidosis (ATTRv) is a heterogeneous disease with a clinical presentation that varies according to geographical area and TTR mutation. The symptoms of Val50Met-ATTRv are mainly neuropathic and prog
Externí odkaz:
https://doaj.org/article/d74163ddd0f643278495d7688ff9e328
Autor:
Mercedes García-Gasalla, Juana M. Ferrer, Pablo A. Fraile-Ribot, Adrián Ferre-Beltrán, Adrián Rodríguez, Natalia Martínez-Pomar, Luisa Ramon-Clar, Amanda Iglesias, Inés Losada-López, Francisco Fanjul, Joan Albert Pou, Isabel Llompart-Alabern, Nuria Toledo, Jaime Pons, Antonio Oliver, Melchor Riera, Javier Murillas
Publikováno v:
Canadian Journal of Infectious Diseases and Medical Microbiology, Vol 2021 (2021)
Background. Early identification of COVID-19 patients at risk of critical illness is a challenging endeavor for clinicians. We aimed to establish immunological, virological, and routine laboratory markers, which, in combination with clinical informat
Externí odkaz:
https://doaj.org/article/93915232cdf24aaf9da6c04a58dbd879
Autor:
Juan González-Moreno, Aina Darder, Inés Losada López, Adrian Rodriguez, Cristina Gomez-Bellvert, Eugenia Cisneros
Publikováno v:
Rheumatology International. 41:2041-2044
Pulmonary nodular lymphoid hyperplasia, also known as pseudolymphoma, is an uncommon reactive lymphoproliferative disorder of unknown etiology that can be found in Sjogren's syndrome patients. Here, we present a case of a previously healthy woman in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c0b778db7b7f00e397ea1f4c852fa66b
https://doi.org/10.1007/s00296-021-04915-2
https://doi.org/10.1007/s00296-021-04915-2
Autor:
Aina Gayà-Barroso, Juan González-Moreno, Adrián Rodríguez, Tomás Ripoll-Vera, Inés Losada-López, Margarita Gili, Milena Paneque, Eugenia Cisneros-Barroso
Publikováno v:
International Journal of Environmental Research and Public Health; Volume 19; Issue 18; Pages: 11721
The purpose of this study was to explore the occupational performance and needs of patients with hereditary transthyretin amyloidosis (ATTRv). A semi-structured interview was conducted by an occupational therapist with 44 patients with Val50Met-ATTRv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::561f5882e164e5b9f5d6414c75375d89
https://pubmed.ncbi.nlm.nih.gov/36141995
https://pubmed.ncbi.nlm.nih.gov/36141995
Autor:
Inés Losada López, Mercedes García Gasalla, Juan González Moreno, Araceli Serrano, Francisco Javier Domínguez Valdés, Joan Milà, Antoni Payeras
Publikováno v:
European Journal of Inflammation, Vol 14 (2016)
Low mannose binding lectin (MBL) producer genotypes have been considered as a systemic lupus erythematosus (SLE) risk factor. The aim of this study was to explore whether polymorphisms in the MBL gene are associated with susceptibility to SLE and dis
Externí odkaz:
https://doaj.org/article/ee04eaa387b346adac97c8700e138e18
Autor:
Aina Gayà-Barroso, Juan González-Moreno, Adrián Rodríguez, Tomás Ripoll-Vera, Inés Losada-López, Margarita Gili, Eugenia Cisneros-Barroso
Publikováno v:
International Journal of Environmental Research and Public Health; Volume 19; Issue 8; Pages: 4464
This study was designed to investigate the global utilization of occupational therapy (OT) services by patients with hereditary transthyretin amyloidosis (ATTRv) in Spain. The main objective was to find out whether these patients have access to OT se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ad673f3462727375e6a65eafb520914
https://pubmed.ncbi.nlm.nih.gov/35457333
https://pubmed.ncbi.nlm.nih.gov/35457333
Autor:
Asuncion Ferrer-Nadal, Mercedes Iglesias, Jorge Álvarez Rubio, Juan González Moreno, Tomás Ripoll-Vera, Inés Losada López
Publikováno v:
Revista Española de Cardiología. 74:185-187
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::96ad373d272db411406df985df114c98
https://doi.org/10.1016/j.recesp.2020.05.027
https://doi.org/10.1016/j.recesp.2020.05.027