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Year Number of Results
2015 3
2016 3
2017 3
2018 5
2019 6
2020 5
2021 5
2022 4
2023 6
2024 1

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Page 1
Editorial: Women in pediatric cardiology 2021.
Muiño-Mosquera L, Nordmeyer S. Muiño-Mosquera L, et al. Front Pediatr. 2023 Feb 20;11:1143383. doi: 10.3389/fped.2023.1143383. eCollection 2023. Front Pediatr. 2023. PMID: 36891231 Free PMC article. No abstract available.
Cardiomyopathy in Genetic Aortic Diseases.
Muiño-Mosquera L, De Backer J. Muiño-Mosquera L, et al. Front Pediatr. 2021 Jul 15;9:682390. doi: 10.3389/fped.2021.682390. eCollection 2021. Front Pediatr. 2021. PMID: 34336739 Free PMC article. Review.
Aortic disease in Marfan syndrome is caused by overactivation of sGC-PRKG signaling by NO.
de la Fuente-Alonso A, Toral M, Alfayate A, Ruiz-Rodríguez MJ, Bonzón-Kulichenko E, Teixido-Tura G, Martínez-Martínez S, Méndez-Olivares MJ, López-Maderuelo D, González-Valdés I, Garcia-Izquierdo E, Mingo S, Martín CE, Muiño-Mosquera L, De Backer J, Nistal JF, Forteza A, Evangelista A, Vázquez J, Campanero MR, Redondo JM. de la Fuente-Alonso A, et al. Among authors: muino mosquera l. Nat Commun. 2021 May 11;12(1):2628. doi: 10.1038/s41467-021-22933-3. Nat Commun. 2021. PMID: 33976159 Free PMC article.
EMILIN1 deficiency causes arterial tortuosity with osteopenia and connects impaired elastogenesis with defective collagen fibrillogenesis.
Adamo CS, Beyens A, Schiavinato A, Keene DR, Tufa SF, Mörgelin M, Brinckmann J, Sasaki T, Niehoff A, Dreiner M, Pottie L, Muiño-Mosquera L, Gulec EY, Gezdirici A, Braghetta P, Bonaldo P, Wagener R, Paulsson M, Bornaun H, De Rycke R, De Bruyne M, Baeke F, Devine WP, Gangaram B, Tam A, Balasubramanian M, Ellard S, Moore S, Symoens S, Shen J, Cole S, Schwarze U, Holmes KW, Hayflick SJ, Wiszniewski W, Nampoothiri S, Davis EC, Sakai LY, Sengle G, Callewaert B. Adamo CS, et al. Among authors: muino mosquera l. Am J Hum Genet. 2022 Dec 1;109(12):2230-2252. doi: 10.1016/j.ajhg.2022.10.010. Epub 2022 Nov 8. Am J Hum Genet. 2022. PMID: 36351433 Free PMC article.
Managing aortic aneurysms and dissections during pregnancy.
Muiño Mosquera L, De Backer J. Muiño Mosquera L, et al. Expert Rev Cardiovasc Ther. 2015 Jun;13(6):703-14. doi: 10.1586/14779072.2015.1042862. Epub 2015 May 17. Expert Rev Cardiovasc Ther. 2015. PMID: 26000563 Review.
Genetics in congenital heart disease. Are we ready for it?
De Backer J, Callewaert B, Muiño Mosquera L. De Backer J, et al. Among authors: muino mosquera l. Rev Esp Cardiol (Engl Ed). 2020 Nov;73(11):937-947. doi: 10.1016/j.rec.2020.05.019. Epub 2020 Jul 6. Rev Esp Cardiol (Engl Ed). 2020. PMID: 32646792 Review. English, Spanish.
Physical activity and physical fitness in children with heritable connective tissue disorders.
de Koning L, Warnink-Kavelaars J, van Rossum M, Limmen S, Van der Looven R, Muiño-Mosquera L, van der Hulst A, Oosterlaan J, Rombaut L, Engelbert R; Pediatric Heritable Connective Tissue Disorders Study Group. de Koning L, et al. Among authors: muino mosquera l. Front Pediatr. 2023 Mar 17;11:1057070. doi: 10.3389/fped.2023.1057070. eCollection 2023. Front Pediatr. 2023. PMID: 37009265 Free PMC article.
Angiotensin-II receptor blockade in Marfan syndrome.
Muiño-Mosquera L, De Backer J. Muiño-Mosquera L, et al. Lancet. 2019 Dec 21;394(10216):2206-2207. doi: 10.1016/S0140-6736(19)32536-X. Epub 2019 Dec 10. Lancet. 2019. PMID: 31836197 Free article. No abstract available.
39 results