Source: Orphanet Journal of Rare Diseases. Unidades: FM, EEFE, FMRP
Subjects: CARDIOPATIAS, AMILOIDOSE, DOENÇAS DO SISTEMA NERVOSO PERIFÉRICO, EPIDEMIOLOGIA
ABNT
FERNANDES, Fábio et al. Clinical and genetic profiles of patients with hereditary and wild-type transthyretin amyloidosis: the Transthyretin Cardiac Amyloidosis Registry in the state of São Paulo, Brazil (REACT-SP). Orphanet Journal of Rare Diseases, v. 19, 2024Tradução . . Disponível em: https://doi.org/10.1186/s13023-024-03281-z. Acesso em: 31 out. 2024.APA
Fernandes, F., Luzuriaga, G. del C. J., Fonseca, G. W. P. da, Correia, E. B., Macedo, A. V. S., Coelho-Filho, O. R., et al. (2024). Clinical and genetic profiles of patients with hereditary and wild-type transthyretin amyloidosis: the Transthyretin Cardiac Amyloidosis Registry in the state of São Paulo, Brazil (REACT-SP). Orphanet Journal of Rare Diseases, 19. doi:10.1186/s13023-024-03281-zNLM
Fernandes F, Luzuriaga G del CJ, Fonseca GWP da, Correia EB, Macedo AVS, Coelho-Filho OR, Scheinberg P, Antunes MO, Schwartzmann PV, Mangini S, Marques W, Simões MV. Clinical and genetic profiles of patients with hereditary and wild-type transthyretin amyloidosis: the Transthyretin Cardiac Amyloidosis Registry in the state of São Paulo, Brazil (REACT-SP) [Internet]. Orphanet Journal of Rare Diseases. 2024 ; 19[citado 2024 out. 31 ] Available from: https://doi.org/10.1186/s13023-024-03281-zVancouver
Fernandes F, Luzuriaga G del CJ, Fonseca GWP da, Correia EB, Macedo AVS, Coelho-Filho OR, Scheinberg P, Antunes MO, Schwartzmann PV, Mangini S, Marques W, Simões MV. Clinical and genetic profiles of patients with hereditary and wild-type transthyretin amyloidosis: the Transthyretin Cardiac Amyloidosis Registry in the state of São Paulo, Brazil (REACT-SP) [Internet]. Orphanet Journal of Rare Diseases. 2024 ; 19[citado 2024 out. 31 ] Available from: https://doi.org/10.1186/s13023-024-03281-z