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Combining familial hypercholesterolemia and statin genetic studies as a strategy for the implementation of pharmacogenomics. A multidisciplinary approach.
Ramudo-Cela L, Santana-Martínez S, García-Ramos M, Bergamino M, García-Giustiniani D, Vélez-Vieitez P, Hernández-Hernández JL, García-Ibarbia C, González-Bustos P, Ruíz-Martín P, González-Lozano J, Santomé-Collazo L, Grana-Fernandez A, Cabaleiro-Cerviño P, Ortíz M, Monserrat-Iglesias L. Ramudo-Cela L, et al. Among authors: monserrat iglesias l. Pharmacogenomics J. 2022 May;22(3):180-187. doi: 10.1038/s41397-022-00274-8. Epub 2022 Mar 31. Pharmacogenomics J. 2022. PMID: 35361995
Genotype-phenotype correlations in hypertrophic cardiomyopathy: a multicenter study in Portugal and Spain of the TPM1 p.Arg21Leu variant.
Lamounier Junior A, Guitián González A, Rodríguez Vilela A, Repáraz Andrade A, Rubio Alcaide Á, Berta Sousa A, Benito López C, Alonso García D, Fernández Ferro G, Cruz I, Cárdenas Reyes IJ, Salazar-Mendiguchía García J, Larrañaga-Moreira JM, Ochoa JP, Palomino-Doza J, de la Higuera Romero L, Nicolás Cicerchia M, Restrepo Córdoba MA, Peña-Peña ML, Noël Brögger M, Loureiro M, Mogollón Jiménez MV, Bilbao Quesada R, Franco Gutiérrez R, García Hernández S, Ripoll-Vera T, Fernández X, Azevedo O, García Pavía P, Lopes LR, Ortiz M, Brito D, Barriales-Villa R, Monserrat Iglesias L. Lamounier Junior A, et al. Among authors: monserrat iglesias l. Rev Esp Cardiol (Engl Ed). 2022 Mar;75(3):242-250. doi: 10.1016/j.rec.2021.01.001. Epub 2021 Feb 26. Rev Esp Cardiol (Engl Ed). 2022. PMID: 33642254 English, Spanish.
The R820W mutation in the MYBPC3 gene, associated with hypertrophic cardiomyopathy in cats, causes hypertrophic cardiomyopathy and left ventricular non-compaction in humans.
Ripoll Vera T, Monserrat Iglesias L, Hermida Prieto M, Ortiz M, Rodriguez Garcia I, Govea Callizo N, Gómez Navarro C, Rosell Andreo J, Gámez Martínez JM, Pons Lladó G, Cremer Luengos D, Torres Marqués J. Ripoll Vera T, et al. Among authors: monserrat iglesias l. Int J Cardiol. 2010 Nov 19;145(2):405-407. doi: 10.1016/j.ijcard.2010.04.032. Epub 2010 Jun 14. Int J Cardiol. 2010. PMID: 20542340
The p.Arg118Cys Variant in the GLA Gene Does Not Cause Fabry Disease. More Evidence.
Barbeito-Caamaño C, Cao-Vilariño M, Mosquera-Reboredo J, García-Pavía P, Monserrat-Iglesias L, Barriales-Villa R. Barbeito-Caamaño C, et al. Among authors: monserrat iglesias l. Rev Esp Cardiol (Engl Ed). 2018 Oct;71(10):871-873. doi: 10.1016/j.rec.2017.08.007. Epub 2017 Sep 21. Rev Esp Cardiol (Engl Ed). 2018. PMID: 28941980 English, Spanish. No abstract available.
Cardiac-only Timothy Syndrome (COTS): Peripartum Cardiomyopathy and Long QT Syndrome.
Larrañaga-Moreira JM, Quintela-García S, Cárdenas-Reyes IJ, Barbeito-Caamaño C, Monserrat-Iglesias L, Barriales-Villa R. Larrañaga-Moreira JM, et al. Among authors: monserrat iglesias l. Rev Esp Cardiol (Engl Ed). 2019 Oct;72(10):876-878. doi: 10.1016/j.rec.2019.01.017. Epub 2019 May 13. Rev Esp Cardiol (Engl Ed). 2019. PMID: 31097345 English, Spanish. No abstract available.
[Exercise echocardiography to differentiate dilated cardiomyopathy from ischemic left ventricular dysfunction].
Peteiro Vázquez J, Monserrat Iglesias L, Vázquez Rey E, Calviño Santos R, Vázquez Rodríguez JM, Fabregas Casal R, Salgado Fernández J, Rodríguez-Fernández JA, Castro Beiras A. Peteiro Vázquez J, et al. Among authors: monserrat iglesias l. Rev Esp Cardiol. 2003 Jan;56(1):57-64. doi: 10.1016/s0300-8932(03)76822-5. Rev Esp Cardiol. 2003. PMID: 12550001 Free article. Spanish.
12 results