Phenotypic characterization and long term follow-up of Brazilian patients with progressive external ophthalmoplegia and primary MTDNA mutations (2017)
- Authors:
- USP affiliated authors: SOBREIRA, CLAUDIA FERREIRA DA ROSA - FMRP ; MARQUES JÚNIOR, WILSON - FMRP ; BARREIRA, AMILTON ANTUNES - FMRP
- Unidade: FMRP
- Subjects: MITOCÔNDRIAS; DNA MITOCONDRIAL; PATOLOGIA
- Language: Inglês
- Imprenta:
- Source:
- Título: Abstracts
- Conference titles: International Meeting of Mitochondrial Pathology (EUROMIT)
-
ABNT
CARVALHO, E. et al. Phenotypic characterization and long term follow-up of Brazilian patients with progressive external ophthalmoplegia and primary MTDNA mutations. 2017, Anais.. Cologne: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 2017. . Acesso em: 12 fev. 2026. -
APA
Carvalho, E., Trindade, K. B. B., Marques Júnior, W., Barreira, A. A., & Sobreira, C. F. da R. (2017). Phenotypic characterization and long term follow-up of Brazilian patients with progressive external ophthalmoplegia and primary MTDNA mutations. In Abstracts. Cologne: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. -
NLM
Carvalho E, Trindade KBB, Marques Júnior W, Barreira AA, Sobreira CF da R. Phenotypic characterization and long term follow-up of Brazilian patients with progressive external ophthalmoplegia and primary MTDNA mutations. Abstracts. 2017 ;[citado 2026 fev. 12 ] -
Vancouver
Carvalho E, Trindade KBB, Marques Júnior W, Barreira AA, Sobreira CF da R. Phenotypic characterization and long term follow-up of Brazilian patients with progressive external ophthalmoplegia and primary MTDNA mutations. Abstracts. 2017 ;[citado 2026 fev. 12 ] - Increasing the differential diagnosis of the inherited demyelinating neuropathies with non-uniform nerve conduction(NCS): Andermann syndrome
- Spinocerebellar ataxia with hypogonadism: an intriguing group of genetic disorders
- Spinocerebellar ataxia with hypogonadism: unravelling and overlooked group of inherited metabolic disorders
- Profile of contractures in muscular dystrophies: analysis of 34 proximal and distal movemen
- Quantitative analysis of contractures in mitochondrial myopathies
- Inter-rater reliability among evaluators using the modified medical research council scale and the medical reasearch council scale in the assessment of lower limbs muscle strength of 61 patients
- Myopathy and exercise intolerance associated with the M.3460G>A MTDNA mutation: expanding the phenotype presentation
- Compound Charcot-Marie-Tooth disease may determine unusual and milder phenotypes
- Inter-rater reliability in the evaluation of muscles of the superior limbs using the medical research council (MRC) scale and the modified MRC scale
- Inter-rater reliability among evaluators using the modified medical research council scale and the medical research council scale in the assessment of upper limbs muscle strength of 61 patients
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
