Zobrazeno 1 - 10
of 59
pro vyhledávání: '"Laura Muiño-Mosquera"'
Autor:
Liqun Sun, Laura Muiño-Mosquera
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
Externí odkaz:
https://doaj.org/article/418337378e954c969d39ebf855de9d81
Autor:
Amber Waddell, Sophie Hespe, Babken Asatryan, Emma Owens, Courtney Thaxton, Mhy-Lanie Adduru, Kailyn Anderson, Emily Brown, Lily Hoffman-Andrews, Elizabeth Jordan, Megan Mayers, Stacey Peters, Fergus Stafford, Richard Bagnall, Lucas Bronicki, Bert Callewaert, C. Anwar Chahal, Cynthia James, Olga Jarinova, Andrew Landstrom, Elizabeth McNally, Brittney Murray, Laura Muiño-Mosquera, Victoria Parikh, Chloe Reuter, Roddy Walsh, Bess Wayburn, James Ware, Jodie Ingles
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101047- (2024)
Externí odkaz:
https://doaj.org/article/bd0ce983443640bf8524d486c2542311
Autor:
Rik De Wolf, Mahmoud Zaqout, Kaoru Tanaka, Laura Muiño-Mosquera, Gerlant van Berlaer, Kristof Vandekerckhove, Wendy Dewals, Daniël De Wolf
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
IntroductionMultisystem inflammatory syndrome in children (MIS-C) is associated with important cardiovascular morbidity during the acute phase. Follow-up shows a swift recovery of cardiac abnormalities in most patients. However, a small portion of pa
Externí odkaz:
https://doaj.org/article/216e1711d3624a76b2271aa4de01fa60
Autor:
Lisanne de Koning, Jessica Warnink-Kavelaars, Marion van Rossum, Selina Limmen, Ruth Van der Looven, Laura Muiño-Mosquera, Annelies van der Hulst, Jaap Oosterlaan, Lies Rombaut, Raoul Engelbert, on behalf of the Pediatric Heritable Connective Tissue Disorders Study Group
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
ObjectivesHealth problems in patients with heritable connective tissue disorders (HCTD) are diverse and complex and might lead to lower physical activity (PA) and physical fitness (PF). This study aimed to investigate the PA and PF of children with h
Externí odkaz:
https://doaj.org/article/f589ea41785d418784d7d264ed998e21
Autor:
Laura Muiño-Mosquera, Sarah Nordmeyer
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
Externí odkaz:
https://doaj.org/article/6ce297cce4e64b8fb3c8f8b253a2ac18
Autor:
Andrea de la Fuente-Alonso, Marta Toral, Alvaro Alfayate, María Jesús Ruiz-Rodríguez, Elena Bonzón-Kulichenko, Gisela Teixido-Tura, Sara Martínez-Martínez, María José Méndez-Olivares, Dolores López-Maderuelo, Ileana González-Valdés, Eusebio Garcia-Izquierdo, Susana Mingo, Carlos E. Martín, Laura Muiño-Mosquera, Julie De Backer, J. Francisco Nistal, Alberto Forteza, Arturo Evangelista, Jesús Vázquez, Miguel R. Campanero, Juan Miguel Redondo
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-18 (2021)
Aortic aneurysm and dissection, the major problem linked to Marfan syndrome (MFS), lacks effective pharmacological treatment. Here, the authors show that the NO pathway is overactivated in MFS and that inhibition of guanylate cyclase and cGMP-depende
Externí odkaz:
https://doaj.org/article/439b8e5d5511412680725f97df82754a
Autor:
Laura Muiño-Mosquera, Hans De Wilde, Daniel Devos, Danilo Babin, Luc Jordaens, Anthony Demolder, Katya De Groote, Daniel De Wolf, Julie De Backer
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-11 (2020)
Abstract Background Aortic root dilatation and—dissection and mitral valve prolapse are established cardiovascular manifestations in Marfan syndrome (MFS). Heart failure and arrhythmic sudden cardiac death have emerged as additional causes of morbi
Externí odkaz:
https://doaj.org/article/44c42345486a4e2cb37838d67c6a8b5c
Autor:
Laura Muiño-Mosquera, Julie De Backer
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Genetic aortic diseases are a group of illnesses characterized by aortic aneurysms or dissection in the presence of an underlying genetic defect. They are part of the broader spectrum of heritable thoracic aortic disease, which also includes those ca
Externí odkaz:
https://doaj.org/article/bbfc3fe0769a42998b2c281966a99a09
Autor:
Laura Muiño‐Mosquera, Fré Bauters, Karlien Dhondt, Hans De Wilde, Luc Jordaens, Katya De Groote, Daniel De Wolf, Katrien Hertegonne, Julie De Backer
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 8, Pp n/a-n/a (2019)
Abstract Background Marfan syndrome (MFS) is an inherited connective tissue disorder characterized by ectopia lentis, aortic root dilation and dissection and specific skeletal features. Obstructive sleep apnea (OSA) in MFS has been described earlier
Externí odkaz:
https://doaj.org/article/8b9a4db5e8da401e8b3b6338f23375d9
Myocardial Function, Heart Failure and Arrhythmia in Marfan Syndrome: A Systematic Literature Review
Publikováno v:
Diagnostics, Vol 10, Iss 10, p 751 (2020)
Marfan syndrome (MFS) is a heritable systemic connective tissue disease with important cardiovascular involvement, including aortic root dilatation and mitral valve prolapse. Life expectancy in patients with MFS is mainly determined by cardiovascular
Externí odkaz:
https://doaj.org/article/808dc8f0ab5c46bc88302ebbb15e4ecf