Rod distribution and muscle fiber type modification in the progression of nemaline myopathy (2003)
- Authors:
- USP affiliated authors: REED, UMBERTINA CONTI - FM ; MARIE, SUELY KAZUE NAGAHASHI - FM ; ZATZ, MAYANA - IB ; VAINZOF, MARIZ - IB
- Unidades: FM; IB
- Assunto: NEUROLOGIA
- Language: Inglês
- Imprenta:
- Publisher place: Saint Lois
- Date published: 2003
- Source:
- Título: Journal of Child Neurology
- ISSN: 0883-0738
- Volume/Número/Paginação/Ano: v. 18, n. 3, p. 235-240, 2003
-
ABNT
GURGEL-GIANNETTI, J. et al. Rod distribution and muscle fiber type modification in the progression of nemaline myopathy. Journal of Child Neurology, v. 18, n. 3, p. 235-240, 2003Tradução . . Acesso em: 21 fev. 2026. -
APA
Gurgel-Giannetti, J., Zanoteli, E., Werneck, L. C., Reed, U. C., Beggs, A. H., Marie, S. K. N., et al. (2003). Rod distribution and muscle fiber type modification in the progression of nemaline myopathy. Journal of Child Neurology, 18( 3), 235-240. -
NLM
Gurgel-Giannetti J, Zanoteli E, Werneck LC, Reed UC, Beggs AH, Marie SKN, Fireman MAT, Oliveira ASB, Zatz M, Vainzof M. Rod distribution and muscle fiber type modification in the progression of nemaline myopathy. Journal of Child Neurology. 2003 ; 18( 3): 235-240.[citado 2026 fev. 21 ] -
Vancouver
Gurgel-Giannetti J, Zanoteli E, Werneck LC, Reed UC, Beggs AH, Marie SKN, Fireman MAT, Oliveira ASB, Zatz M, Vainzof M. Rod distribution and muscle fiber type modification in the progression of nemaline myopathy. Journal of Child Neurology. 2003 ; 18( 3): 235-240.[citado 2026 fev. 21 ] - Rod distribution and muscles fibers type modification in the progression of nemaline myopathy
- Estudo imunohistoquímico de proteínas musculares na miopatia nemalínica
- Rods proteic-constituition and muscle fiber maturation in nemaline myopathy
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- Nemaline myopathy (NM) in brazilian patients
- Nebulin expression in patients with nemaline myopathy
- Necklace fibers as histopathological marker in a patient with severe form of X-linked myotubular myopathy
- Dominant or recessive mutations in the RYR1 gene causing central core myopathy in Brazilian patients
- Relevance of the A8344G and T8356C mtDNA mutation analyses in the approach of progressive myoclonic epilepsy
- Expressão da nebulina em pacientes com miopatia nemalínica
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