Pearls & Oy-sters [Editorial]: A curable myopathy manifesting as exercise intolerance and respiratory failure (2018)
- Authors:
- Autor USP: ZANOTELI, EDMAR - FM
- Unidade: FM
- DOI: 10.1212/WNL.0000000000005867
- Subjects: MUTAÇÃO GENÉTICA; INSUFICIÊNCIA RESPIRATÓRIA; BIÓPSIA; MÚSCULOS
- Language: Inglês
- Imprenta:
- Publisher place: Philadelphia
- Date published: 2018
- Source:
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: bronze
-
ABNT
SILVA, Andre M. S. et al. Pearls & Oy-sters [Editorial]: A curable myopathy manifesting as exercise intolerance and respiratory failure. Neurology. Philadelphia: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1212/WNL.0000000000005867. Acesso em: 30 set. 2024. , 2018 -
APA
Silva, A. M. S., Zanoteli, E., Mendonça, R. H., Soares, D. C., Callegaro, D., Caldas, V. M., et al. (2018). Pearls & Oy-sters [Editorial]: A curable myopathy manifesting as exercise intolerance and respiratory failure. Neurology. Philadelphia: Faculdade de Medicina, Universidade de São Paulo. doi:10.1212/WNL.0000000000005867 -
NLM
Silva AMS, Zanoteli E, Mendonça RH, Soares DC, Callegaro D, Caldas VM, Perissinotti IN, Carvalho MS. Pearls & Oy-sters [Editorial]: A curable myopathy manifesting as exercise intolerance and respiratory failure [Internet]. Neurology. 2018 ; 91( 4): 187-190.[citado 2024 set. 30 ] Available from: https://doi.org/10.1212/WNL.0000000000005867 -
Vancouver
Silva AMS, Zanoteli E, Mendonça RH, Soares DC, Callegaro D, Caldas VM, Perissinotti IN, Carvalho MS. Pearls & Oy-sters [Editorial]: A curable myopathy manifesting as exercise intolerance and respiratory failure [Internet]. Neurology. 2018 ; 91( 4): 187-190.[citado 2024 set. 30 ] Available from: https://doi.org/10.1212/WNL.0000000000005867 - Myopathy due to HMGCR antibodies in adult mimicking muscular dystrophy associated with cancer and statin exposure - narrative review of the literature - case report
- Diagnostic yield of multi-gene panel for muscular dystrophies and other hereditary myopathies
- Genotype-phenotype correlations in valosin-containing protein disease: a retrospective muticentre study
- Whole-Body MRI in Limb Girdle Muscular Dystrophy Type R1/2A: Correlation With Clinical Scores
- Rhabdomyolysis: a genetic perspective
- A new mutation in PYGM causing McArdle disease in a Brazilian patient [Carta]
- Myasthenia gravis and COVID-19: clinical characteristics and outcomes
- STAC3 variants cause a congenital myopathy with distinctive dysmorphic features and malignant hyperthermia susceptibility
- Therapeutic advances in 5q-linked spinal muscular atrophy
- Affected female carriers of MTM1 mutations display a wide spectrum of clinical and pathological involvement: delineating diagnostic clues
Informações sobre o DOI: 10.1212/WNL.0000000000005867 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas