Clinical and histological features of brazilian patients with nemaline myopathy (2014)
- Authors:
- USP affiliated authors: ZANOTELI, EDMAR - FM ; REED, UMBERTINA CONTI - FM
- Unidade: FM
- Subjects: BIÓPSIA; BRASILEIROS; MÚSCULOS (FISIOPATOLOGIA); MIOPATIAS CONGÊNITAS ESTRUTURAIS
- Language: Inglês
- Imprenta:
- Source:
- Título: Arquivos de Neuro-Psiquiatria
- ISSN: 0004-282X
- Volume/Número/Paginação/Ano: v. 72, supl. 2, p. 92-93, res. P-211, 2014
- Conference titles: Congresso Brasileiro de Neurologia
-
ABNT
MARTINS, C. A. et al. Clinical and histological features of brazilian patients with nemaline myopathy. Arquivos de Neuro-Psiquiatria. São Paulo: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 11 mar. 2026. , 2014 -
APA
Martins, C. A., Abath Neto, O. L., Carvalho, M., Oliveira, A. S. B., Fireman, M., Reed, U. C., & Zanoteli, E. (2014). Clinical and histological features of brazilian patients with nemaline myopathy. Arquivos de Neuro-Psiquiatria. São Paulo: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Martins CA, Abath Neto OL, Carvalho M, Oliveira ASB, Fireman M, Reed UC, Zanoteli E. Clinical and histological features of brazilian patients with nemaline myopathy. Arquivos de Neuro-Psiquiatria. 2014 ; 72 92-93.[citado 2026 mar. 11 ] -
Vancouver
Martins CA, Abath Neto OL, Carvalho M, Oliveira ASB, Fireman M, Reed UC, Zanoteli E. Clinical and histological features of brazilian patients with nemaline myopathy. Arquivos de Neuro-Psiquiatria. 2014 ; 72 92-93.[citado 2026 mar. 11 ] - Common and variable clinical, histological, and imaging findings of recessive RYR1-related centronuclear myopathy patients
- The clinical spectrum of the congenital myasthenic syndrome resulting from COL13A1 mutations
- Clinical and molecular findings in a cohort of ANO5-related myopathy
- Muscle biopsy with dystrophic pattern and rimmed vacuoles: GNE myopathy in a Brazilian patient
- Theraputic advances in 5q-linked spinal muscular atrophy
- Phenotypic Intermediate Forms Overlapping to Emery-Dreifuss and Limb Girdle Muscular Dystrophies Caused by Lamin A/C Gene Mutations
- Clinical and imaging hallmarks of the MYH7-related myopathy with severe axial involvement
- Clinicogenetic lessons from 370 patients with autosomal recessive limb-girdle muscular dystrophy
- Global Central Nervous System Atrophy in Spinal Muscular Atrophy Type 0 [Carta]
- A novel ATP1A2 mutation in a patient with hypokalaemic periodic paralysis and CNS symptoms
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas