The value of cardiovascular magnetic resonance in the follow-up of Duchenne/Becker muscular dystrophy (2010)
- Authors:
- USP affiliated authors: VAINZOF, MARIZ - IB ; ZATZ, MAYANA - IB
- Unidade: IB
- Subjects: DISTROFIA MUSCULAR; RESSONÂNCIA MAGNÉTICA
- Language: Inglês
- Imprenta:
- Publisher place: Ospedaletto
- Date published: 2010
- Source:
- Título do periódico: Acta Myologica
- ISSN: 1128-2460
- Volume/Número/Paginação/Ano: v. 29, p. 99 res.S6.PP2, 2010
- Conference titles: International Congress on Neuromuscular Diseases (ICNMD)
-
ABNT
GURGEL-GIANNETTI, Juliana et al. The value of cardiovascular magnetic resonance in the follow-up of Duchenne/Becker muscular dystrophy. Acta Myologica. Ospedaletto: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 23 abr. 2024. , 2010 -
APA
Gurgel-Giannetti, J., Silva, M., Meira, Z., Ferreira, R. A., Yamamoto, L. U., Vainzof, M., et al. (2010). The value of cardiovascular magnetic resonance in the follow-up of Duchenne/Becker muscular dystrophy. Acta Myologica. Ospedaletto: Instituto de Biociências, Universidade de São Paulo. -
NLM
Gurgel-Giannetti J, Silva M, Meira Z, Ferreira RA, Yamamoto LU, Vainzof M, Zatz M, Rochitte CE. The value of cardiovascular magnetic resonance in the follow-up of Duchenne/Becker muscular dystrophy. Acta Myologica. 2010 ; 29 99 res.S6.PP2.[citado 2024 abr. 23 ] -
Vancouver
Gurgel-Giannetti J, Silva M, Meira Z, Ferreira RA, Yamamoto LU, Vainzof M, Zatz M, Rochitte CE. The value of cardiovascular magnetic resonance in the follow-up of Duchenne/Becker muscular dystrophy. Acta Myologica. 2010 ; 29 99 res.S6.PP2.[citado 2024 abr. 23 ] - Partial telethonin deficiency in severely affected North American limb girdle muscular dystrophy patients
- Duchenne clinically discordant brothers: a "Ringo-like" phenotype in humans?
- Um novo locus para uma forma tardia de doença do neurônio motor/esclerose lateral aminotrófica
- Calpainopatia: surpresas nos estudos de correlação genótipo: fenótipo
- Expressão de distrofia em co-culturas de células-tronco de cordão umbilical e mioblastos de pacientes afetados pela DMD
- Ringo:: discordance between the molecular and clinical manifestation in a Golden Retriever muscular dystrophy dog
- Sarcoglycanopathies: a multiplex molecular analysis for the most common mutations
- Central core disease due to recessive mutations in RYR1 gene: is it more common than described?
- Muscular dystrophies and protein mutations
- Central core disease (CCD): improving the screening for mutations in RYR1 gene
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas