Clinical and Histologic Findings in ACTA1-Related Nemaline Myopathy: Case Series and Review of the Literature (2017)
- Autores:
- Autores USP: REED, UMBERTINA CONTI - FM ; ZANOTELI, EDMAR - FM
- Unidade: FM
- DOI: 10.1016/j.pediatrneurol.2017.04.002
- Assuntos: DOENÇAS CONGÊNITAS; MUTAÇÃO GÊNICA; ESTUDOS DE COORTES; MIOPATIA; REVISÃO SISTEMÁTICA
- Idioma: Inglês
- Imprenta:
- Local: Chippewa Falls (US)
- Data de publicação: 2017
- Fonte:
- Título do periódico: Pediatric Neurology
- ISSN: 0887-8994
- Volume/Número/Paginação/Ano: v. 75, p. 11-16, 2017
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
MORENO, Cristiane de Araújo Martins et al. Clinical and Histologic Findings in ACTA1-Related Nemaline Myopathy: Case Series and Review of the Literature. Pediatric Neurology, v. 75, p. 11-16, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.pediatrneurol.2017.04.002. Acesso em: 16 abr. 2024. -
APA
Moreno, C. de A. M., Abath Neto, O., Donkervoort, S., Reed, U. C., Oliveira, A. S. B., Bönnemann, C., & Zanoteli, E. (2017). Clinical and Histologic Findings in ACTA1-Related Nemaline Myopathy: Case Series and Review of the Literature. Pediatric Neurology, 75, 11-16. doi:10.1016/j.pediatrneurol.2017.04.002 -
NLM
Moreno C de AM, Abath Neto O, Donkervoort S, Reed UC, Oliveira ASB, Bönnemann C, Zanoteli E. Clinical and Histologic Findings in ACTA1-Related Nemaline Myopathy: Case Series and Review of the Literature [Internet]. Pediatric Neurology. 2017 ; 75 11-16.[citado 2024 abr. 16 ] Available from: https://doi.org/10.1016/j.pediatrneurol.2017.04.002 -
Vancouver
Moreno C de AM, Abath Neto O, Donkervoort S, Reed UC, Oliveira ASB, Bönnemann C, Zanoteli E. Clinical and Histologic Findings in ACTA1-Related Nemaline Myopathy: Case Series and Review of the Literature [Internet]. Pediatric Neurology. 2017 ; 75 11-16.[citado 2024 abr. 16 ] Available from: https://doi.org/10.1016/j.pediatrneurol.2017.04.002 - Clinical and imaging hallmarks of the MYH7-related myopathy with severe axial involvement
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- A novel acta 1 mutation in a patient with nemaline myopathy
- Clinical and histological features of brazilian patients with nemaline myopathy
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- Congenital fiber type disproportion caused by TPM3 mutation: a report of two atypical cases
- Clinicogenetic lessons from 370 patients with autosomal recessive limb-girdle muscular dystrophy
- Global Central Nervous System Atrophy in Spinal Muscular Atrophy Type 0 [Carta]
- Muscle biopsy with dystrophic pattern and rimmed vacuoles: GNE myopathy in a Brazilian patient
- Distrofias musculares e miopatias congênitas
Informações sobre o DOI: 10.1016/j.pediatrneurol.2017.04.002 (Fonte: oaDOI API)
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