Results 21 to 30 of about 160 (89)

Position Statement on Diagnosis and Treatment of Cardiac Amyloidosis - 2021. [PDF]

Arq Bras Cardiol, 2021
Simões MV, Fernandes F, Marcondes-Braga FG, Scheinberg P, Correia EB, Rohde LEP, Bacal F, Alves SMM, Mangini S, Biolo A, Beck-da-Silva L, Szor RS, Marques Junior W, Oliveira ASB, Cruz MW, Bueno BVK, Hajjar LA, Issa AFC, Ramires FJA, Coelho Filho OR, Schmidt A, Pinto IMF, Rochitte CE, Vieira MLC, Mesquita CT, Ramos CD, Soares-Junior J, Romano MMD, Mathias Junior W, Garcia Junior MI, Montera MW, Melo MDT, Silva SME, Garibaldi PMM, Alencar Neto AC, Lopes RD, Ávila DX, Viana D, Saraiva JFK, Canesin MF, Oliveira GMM, Mesquita ET.   +41 more
europepmc   +1 more source

Left Ventricular Hypertrophy: One Phenotype, Two Hypotheses, Three Lessons. [PDF]

Arq Bras Cardiol, 2021
Rodrigues P, Soares AR, Taipa R, Ferreira S, Reis H.   +4 more
europepmc   +1 more source

Position Statement on the Use of Myocardial Strain in Cardiology Routines by the Brazilian Society of Cardiology's Department Of Cardiovascular Imaging - 2023. [PDF]

Arq Bras Cardiol, 2023
Almeida ALC, Melo MDT, Bihan DCSL, Vieira MLC, Pena JLB, Del Castillo JM, Abensur H, Hortegal RA, Otto MEB, Piveta RB, Dantas MR, Assef JE, Beck ALS, Santo THCE, Silva TO, Salemi VMC, Rocon C, Lima MSM, Barberato SH, Rodrigues AC, Rabschkowisky A, Frota DDCR, Gripp EA, Barretto RBM, Silva SME, Cauduro SA, Pinheiro AC, Araujo SP, Tressino CG, Silva CES, Monaco CG, Paiva MG, Fisher CH, Alves MSL, Grau CRPC, Santos MVCD, Guimarães ICB, Morhy SS, Leal GN, Soares AM, Cruz CBBV, Guimarães Filho FV, Assunção BMBL, Fernandes RM, Saraiva RM, Tsutsui JM, Soares FLJ, Falcão SNDRS, Hotta VT, Armstrong ADC, Hygidio DA, Miglioranza MH, Camarozano AC, Lopes MMU, Cerci RJ, Siqueira MEM, Torreão JA, Rochitte CE, Felix A.   +58 more
europepmc   +1 more source

Transthyretin Amyloid Cardiomyopathy Mimicking Hypertrophic Cardiomyopathy in an Older Patient. [PDF]

Arq Bras Cardiol, 2021
Guimarães JPA, Trigo J, Gonçalves F, Moreira JI.   +3 more
europepmc   +1 more source

Amiloidose e o aparelho respiratorio.

Acta Médica Portuguesa, 2009
Amyloidosis is a disease of protein metabolism characterized by the deposition of amyloid substance in several organs. Several types of amyloid protein exist and one of the possible classifications is primary, secondary or hereditary amyloidosis, based on the type of protein involved and whether there is another condition that leads to amyloidosis. One
Teresa Costa, Vitória Martins, Yvette Martins, Jorge Pires   +3 more
openaire   +1 more source

The Challenge of Making Cardiac Resonance a Global Reality. [PDF]

Arq Bras Cardiol, 2023
Gomes HJA, Figueredo Junior AR.
europepmc   +1 more source

Hereditary transthyretin-mediated amyloidosis with polyneuropathy: baseline anthropometric, demographic and disease characteristics of patients from a reference center. [PDF]

Arq Neuropsiquiatr, 2022
Sequeira VCC, Penetra MA, Duarte L, Azevedo FR, Sayegh RSR, Pedrosa RC, Cruz MW.   +6 more
europepmc   +1 more source

Transdisciplinarity in the approach to amyloidosis. [PDF]

Rev Fac Cien Med Univ Nac Cordoba, 2021
Alfonsín AE, Escada SS, Kohan D, Valeo Chulvi MP, Posadas Martínez ML, Aguirre MA, Nucifora EM.   +6 more
europepmc   +1 more source

Nuclear Cardiology in the Optimization of Resynchronization Therapy: Quo Vadis? [PDF]

Arq Bras Cardiol, 2023
Grossman GB.
europepmc   +1 more source

Apical Sparing and Granular Sparkling: Not Everything that Glitters Is Cardiac Amyloidosis. [PDF]

Arq Bras Cardiol
Barros APM, Romero CE, Cardoso JN, Fernandes F, Hotta VT.   +4 more
europepmc   +1 more source