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Portuguese WGMPD Recommendations and consensus documents on Transthyretin Amyloidotic Cardiomyopathy
Páginas 1-68 (fevereiro 2025)
Editorials
Cardiac amyloidosis: Upcoming challenges for appropriate diagnosis and treatment
Mário Oliveira
Rev Port Cardiol. 2025;44 Supl 1:1
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Portuguese recommendations on transthyretin amyloid cardiomyopathy: A step toward disease awareness, prompt referral and early diagnosis and treatment
Nuno Marques, Olga Azevedo
Rev Port Cardiol. 2025;44 Supl 1:3-5
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Guidelines
Portuguese recommendations for the management of transthyretin amyloid cardiomyopathy (Part 1 of 2): Screening, diagnosis and treatment. Developed by the Task Force on the management of transthyretin amyloid cardiomyopathy of the Working Group on Myocardial and Pericardial Diseases of the Portuguese Society of Cardiology
Nuno Marques, Sílvia Aguiar Rosa, Filipa Cordeiro, Raquel Menezes Fernandes, Catarina Ferreira, Dina Bento, Dulce Brito, Nuno Cardim, ... Olga Azevedo
Rev Port Cardiol. 2025;44 Supl 1:7-48
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Targeted disease-specific therapy for patients with hereditary transthyretin amyloidosis and cardiac involvement after orthotopic liver transplantation. Consensus from the Working Group on Myocardial and Pericardial Diseases of the Portuguese Society of Cardiology and National Reference Centers for Familial Amyloidosis
Sílvia Aguiar Rosa, Catarina Ferreira, Isabel Conceição, Teresa Coelho, Nuno Marques, Olga Azevedo
Rev Port Cardiol. 2025;44 Supl 1:49-57
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Suspicion and referral of patients with transthyretin amyloid cardiomyopathy: Recommendations by a Portuguese multidisciplinary expert panel
Dulce Brito, João Agostinho, Carlos Aguiar, Sílvia Aguiar Rosa, Nuno Cardim, Cândida Fonseca, Nuno Marques, Pedro Moraes Sarmento, ... Olga Azevedo
Rev Port Cardiol. 2025;44 Supl 1:59-68
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