RYR1-related exertional rhabdomyolysis: Expanding spectrum and diagnostic challenges (2015)
- Authors:
- USP affiliated authors: REED, UMBERTINA CONTI - FM ; ZANOTELI, EDMAR - FM
- Unidade: FM
- DOI: 10.1016/j.nmd.2015.06.263
- Subjects: DOENÇAS MUSCULARES; PROTEÍNAS MUSCULARES; DOENÇAS MUSCULOSQUELÉTICAS
- Language: Inglês
- Imprenta:
- Source:
- Título: Neuromuscular Disorders
- ISSN: 0960-8966
- Volume/Número/Paginação/Ano: v. 25, suppl. 2, p. S257-S258, res. G.P.238, 2015
- Conference titles: International Congress of the World Muscle Society
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
GARDINER, A. et al. RYR1-related exertional rhabdomyolysis: Expanding spectrum and diagnostic challenges. Neuromuscular Disorders. London: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.nmd.2015.06.263. Acesso em: 31 dez. 2025. , 2015 -
APA
Gardiner, A., Scalco, R., Parton, M., Hanna, M., Pitceathly, R., Zanoteli, E., et al. (2015). RYR1-related exertional rhabdomyolysis: Expanding spectrum and diagnostic challenges. Neuromuscular Disorders. London: Faculdade de Medicina, Universidade de São Paulo. doi:10.1016/j.nmd.2015.06.263 -
NLM
Gardiner A, Scalco R, Parton M, Hanna M, Pitceathly R, Zanoteli E, Murphy E, Treves S, Houlden H, Wilmshurst J, Straub V, Hilton-Jones D, Voermans N, Manzur A, Oflazer P, Reed U, Lachmann R, Quinlivan R, Jungbluth H. RYR1-related exertional rhabdomyolysis: Expanding spectrum and diagnostic challenges [Internet]. Neuromuscular Disorders. 2015 ; 25 S257-S258.[citado 2025 dez. 31 ] Available from: https://doi.org/10.1016/j.nmd.2015.06.263 -
Vancouver
Gardiner A, Scalco R, Parton M, Hanna M, Pitceathly R, Zanoteli E, Murphy E, Treves S, Houlden H, Wilmshurst J, Straub V, Hilton-Jones D, Voermans N, Manzur A, Oflazer P, Reed U, Lachmann R, Quinlivan R, Jungbluth H. RYR1-related exertional rhabdomyolysis: Expanding spectrum and diagnostic challenges [Internet]. Neuromuscular Disorders. 2015 ; 25 S257-S258.[citado 2025 dez. 31 ] Available from: https://doi.org/10.1016/j.nmd.2015.06.263 - A novel acta 1 mutation in a patient with nemaline myopathy
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Informações sobre o DOI: 10.1016/j.nmd.2015.06.263 (Fonte: oaDOI API)
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