Cardiovascular manifestations in idiopathic inflammatory myopathies (2023)
- Authors:
- Autor USP: SHINJO, SAMUEL KATSUYUKI - FM
- Unidade: FM
- DOI: 10.1007/s10067-023-06599-4
- Subjects: DOENÇAS CARDIOVASCULARES; MIOSITE; DOENÇAS AUTOIMUNES
- Language: Inglês
- Imprenta:
- Source:
- Título: Clinical rheumatology
- ISSN: 0770-3198
- Volume/Número/Paginação/Ano: v. 42, n. 10, p. 2557-2575, 2023
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: hybrid
- Licença: cc-by
-
ABNT
SHAH, Meera et al. Cardiovascular manifestations in idiopathic inflammatory myopathies. Clinical rheumatology, v. 42, n. 10, p. 2557-2575, 2023Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/55992. Acesso em: 19 nov. 2024. -
APA
Shah, M., Shinjo, S. K., Day, J., & Gupta, L. (2023). Cardiovascular manifestations in idiopathic inflammatory myopathies. Clinical rheumatology, 42( 10), 2557-2575. doi:10.1007/s10067-023-06599-4 -
NLM
Shah M, Shinjo SK, Day J, Gupta L. Cardiovascular manifestations in idiopathic inflammatory myopathies [Internet]. Clinical rheumatology. 2023 ; 42( 10): 2557-2575.[citado 2024 nov. 19 ] Available from: https://observatorio.fm.usp.br/handle/OPI/55992 -
Vancouver
Shah M, Shinjo SK, Day J, Gupta L. Cardiovascular manifestations in idiopathic inflammatory myopathies [Internet]. Clinical rheumatology. 2023 ; 42( 10): 2557-2575.[citado 2024 nov. 19 ] Available from: https://observatorio.fm.usp.br/handle/OPI/55992 - Miopatias autoimunes sistêmicas
- Dor em reumatologia
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- Physical exercise among patients with systemic autoimmune myopathies
- Muscle biopsies in dermatomyositis and polymyositis: practical relevance of analyzing different levels of histological sections of the same muscular compartment
- Intravenous human immunoglobulin and/or methylprednisolone pulse therapies as a possible treat-to-target strategy in immune-mediated necrotizing myopathies
- Frequency and clinical relevance of anti-Mi-2 autoantibody in adult Brazilian patients with dermatomyositis
Informações sobre o DOI: 10.1007/s10067-023-06599-4 (Fonte: oaDOI API)
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