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Phenotypic Expression and Outcomes in Patients with the p.Arg301Gln GLA Variant in Anderson-Fabry Disease.
Blanco R, Rico-Ramírez Y, Hermida-Ameijeiras Á, Abdullah IMS, Lau K, Alvarez-Rubio J, Fortuny E, Martínez-Monzonís A, Nowak A, Nordbeck P, Veras-Burgos C, Pons-Llinares J, Rossi E, Caimi-Martínez F, Bosch-Rovira T, Alamar-Cervera M, Ruiz-Pizarro V, Torres-Juan L, Heine-Suñer D, Ripoll-Vera T. Blanco R, et al. Among authors: heine suner d. Int J Mol Sci. 2024 Apr 12;25(8):4299. doi: 10.3390/ijms25084299. Int J Mol Sci. 2024. PMID: 38673884 Free PMC article.
New Variant in Placophilin-2 Gene Causing Arrhythmogenic Myocardiopathy.
Caimi-Martinez F, Antoniutti G, Blanco R, García de la Villa B, Alvarenga N, Govea-Callizo N, Torres-Juan L, Heine-Suñer D, Rosell-Andreo J, Luengos DC, Alvarez-Rubio J, Ripoll-Vera T. Caimi-Martinez F, et al. Among authors: heine suner d. Genes (Basel). 2022 Apr 27;13(5):782. doi: 10.3390/genes13050782. Genes (Basel). 2022. PMID: 35627167 Free PMC article.
Case Report: A Novel NKX2-5 Mutation in a Family With Congenital Heart Defects, Left Ventricular Non-compaction, Conduction Disease, and Sudden Cardiac Death.
Morlanes-Gracia P, Antoniutti G, Alvarez-Rubio J, Torres-Juan L, Heine-Suñer D, Ripoll-Vera T. Morlanes-Gracia P, et al. Among authors: heine suner d. Front Cardiovasc Med. 2021 Jul 1;8:691203. doi: 10.3389/fcvm.2021.691203. eCollection 2021. Front Cardiovasc Med. 2021. PMID: 34277740 Free PMC article.
Propionic acidemia: a rare cause of dilated cardiomyopathy and long QT syndrome.
Siquier-Padilla J, Pons Llinares J, Grau Sepúlveda A, Heine-Suñer D, Massot-Cladera M, Peral Disdier V. Siquier-Padilla J, et al. Among authors: heine suner d. Rev Esp Cardiol (Engl Ed). 2023 Feb;76(2):129-132. doi: 10.1016/j.rec.2022.09.002. Epub 2022 Sep 17. Rev Esp Cardiol (Engl Ed). 2023. PMID: 36126866 English, Spanish. No abstract available.
54 results