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Fabry Disease and the Heart: A Comprehensive Review.
Azevedo O, Cordeiro F, Gago MF, Miltenberger-Miltenyi G, Ferreira C, Sousa N, Cunha D. Azevedo O, et al. Among authors: miltenberger miltenyi g. Int J Mol Sci. 2021 Apr 23;22(9):4434. doi: 10.3390/ijms22094434. Int J Mol Sci. 2021. PMID: 33922740 Free PMC article. Review.
Screening for Fabry disease in patients with left ventricular noncompaction.
Azevedo O, Marques N, Craveiro N, Pereira AR, Antunes H, Reis L, Guerreiro RA, Pontes Dos Santos R, Miltenberger-Miltenyi G, Sousa N, Cunha D. Azevedo O, et al. Rev Port Cardiol (Engl Ed). 2019 Oct;38(10):709-716. doi: 10.1016/j.repc.2019.02.014. Epub 2020 Jan 1. Rev Port Cardiol (Engl Ed). 2019. PMID: 31901299 Free article. English, Portuguese.
Natural history of the late-onset phenotype of Fabry disease due to the p.F113L mutation.
Azevedo O, Gago MF, Miltenberger-Miltenyi G, Robles AR, Costa MA, Pereira O, Vide AT, Castelo Branco G, Simões S, Guimarães MJ, Salgado A, Sousa N, Cunha D. Azevedo O, et al. Mol Genet Metab Rep. 2020 Feb 15;22:100565. doi: 10.1016/j.ymgmr.2020.100565. eCollection 2020 Mar. Mol Genet Metab Rep. 2020. PMID: 32099817 Free PMC article.
Predictors of Fabry disease in patients with hypertrophic cardiomyopathy: How to guide the diagnostic strategy?
Azevedo O, Marques N, Reis L, Cruz I, Craveiro N, Antunes H, Lourenço C, Gomes R, Guerreiro RA, Faria R, Sá F, Lima R, Gaspar P, Faria R, Miltenberger-Miltenyi G, Sousa N, Cunha D; group of investigators. Azevedo O, et al. Among authors: miltenberger miltenyi g. Am Heart J. 2020 Aug;226:114-126. doi: 10.1016/j.ahj.2020.04.006. Epub 2020 Apr 18. Am Heart J. 2020. PMID: 32531501 Free article.
Fabry Disease Therapy: State-of-the-Art and Current Challenges.
Azevedo O, Gago MF, Miltenberger-Miltenyi G, Sousa N, Cunha D. Azevedo O, et al. Among authors: miltenberger miltenyi g. Int J Mol Sci. 2020 Dec 28;22(1):206. doi: 10.3390/ijms22010206. Int J Mol Sci. 2020. PMID: 33379210 Free PMC article. Review.
Left ventricular noncompaction associated with a pathogenic mutation in the MYH7 gene: Known mutation, different phenotype.
Oliveira M, Azevedo O, Faria B, von Hafe P, Dias G, Faria R, Sanfins V, Lourenço M, Miltenberger-Miltenyi G, Lourenço A. Oliveira M, et al. Among authors: miltenberger miltenyi g. Rev Port Cardiol. 2022 Mar;41(3):253-259. doi: 10.1016/j.repc.2018.09.018. Epub 2022 Feb 25. Rev Port Cardiol. 2022. PMID: 36062655 Free article. English, Portuguese.
60 results