Madeira H - Search Results

1

Malignant mutations in hypertrophic cardiomyopathy: fact or fancy?

Brito D, Madeira H. Brito D, et al. Among authors: madeira h. Rev Port Cardiol. 2005 Sep;24(9):1137-46. Rev Port Cardiol. 2005. PMID: 16335287 Review. English, Portuguese.

2

Cardiac Anderson-Fabry disease: lessons from a 25-year-follow up.

Brito D, Miltenberger-Miltenyi G, Moldovan O, Navarro C, Madeira HC. Brito D, et al. Rev Port Cardiol. 2014 Apr;33(4):247.e1-7. doi: 10.1016/j.repc.2013.10.014. Epub 2014 May 13. Rev Port Cardiol. 2014. PMID: 24830310 Free article.

3

Plasma N-terminal pro-brain natriuretic peptide: a marker of left ventricular hypertrophy in hypertrophic cardiomyopathy.

Brito D, Matias JS, Sargento L, Cabral MJ, Madeira HC. Brito D, et al. Rev Port Cardiol. 2004 Dec;23(12):1557-82. Rev Port Cardiol. 2004. PMID: 15732658 English, Portuguese.

4

Dilated cardiomyopathy due to endocrine dysfunction.

Brito D, Pedro M, Bordalo A, Orgando AL, Aguiar A, Gouveia R, Martins AP, Vagueiro MC, Madeira H. Brito D, et al. Among authors: madeira h. Rev Port Cardiol. 2003 Mar;22(3):377-87. Rev Port Cardiol. 2003. PMID: 12847879 English, Portuguese.

5

Familial hypertrophic cardiomyopathy: the same mutation, different prognosis. Comparison of two families with a long follow-up.

Brito D, Richard P, Isnard R, Pipa J, Komajda M, Madeira H. Brito D, et al. Among authors: madeira h. Rev Port Cardiol. 2003 Dec;22(12):1445-61. Rev Port Cardiol. 2003. PMID: 15008060 English, Portuguese.

6

Evaluation of the clinical, hemodynamic and neurohormonal response to levosimendan administration in decompensated heart failure patients. One-month follow-up.

Sargento L, Brito D, Matias JS, Madeira H. Sargento L, et al. Among authors: madeira h. Rev Port Cardiol. 2007 Jul-Aug;26(7-8):717-26. Rev Port Cardiol. 2007. PMID: 17939581 English, Portuguese.

7

Familial and sporadic hypertrophic myopathy: differences and similarities in a genotyped population. A long follow-up study.

Brito D, Richard P, Komajda M, Madeira H. Brito D, et al. Among authors: madeira h. Rev Port Cardiol. 2008 Feb;27(2):147-73. Rev Port Cardiol. 2008. PMID: 18488914 English, Portuguese.

8

Portuguese study of familial dilated cardiomyopathy: the FATIMA study.

Martins E, Silva-Cardoso J, Bicho M, Bourbon M, Ceia F, Rebocho MJ, Moura B, Fonseca C, Correia MJ, Brito D, Perdigão C, Madeira H, Abreu-Lima C. Martins E, et al. Among authors: madeira h. Rev Port Cardiol. 2008 Sep;27(9):1029-42. Rev Port Cardiol. 2008. PMID: 19044174 English, Portuguese.

9

Left ventricular non-compaction: a new mutation predisposing to reverse remodeling?

Cortez-Dias N, Varela MG, Sargento L, Brito D, Almeida A, Cerqueira R, Lança V, Fernandes AR, Tavares P, Pereira RA, Fernandes A, Madeira H. Cortez-Dias N, et al. Among authors: madeira h. Rev Port Cardiol. 2009 Feb;28(2):185-94. Rev Port Cardiol. 2009. PMID: 19438153 English, Portuguese.

10

Genetic diagnosis of hypertrophic cardiomyopathy using mass spectrometry DNA arrays and high resolution melting.

Santos S, Lança V, Oliveira H, Branco P, Silveira L, Marques V, Brito D, Madeira H, Bicho M, Fernandes AR. Santos S, et al. Among authors: madeira h. Rev Port Cardiol. 2011 Jan;30(1):7-18. Rev Port Cardiol. 2011. PMID: 21425739

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