Rod distribution and muscles fibers type modification in the progression of nemaline myopathy (2002)
- 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:
- Source:
- Título: Neuromuscular Disorders
- ISSN: 0960-8966
- Volume/Número/Paginação/Ano: v. 12, n. 7-8, p. 767 res. G.P.6.11, Oct. 2002
- Conference titles: International Congress of the World Muscle Society
-
ABNT
GURGEL-GIANNETTI, J. et al. Rod distribution and muscles fibers type modification in the progression of nemaline myopathy. Neuromuscular Disorders. Oxford: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 22 fev. 2026. , 2002 -
APA
Gurgel-Giannetti, J., Zanoteli, E., Werneck, L. C., Reed, U. C., Beggs, A. H., Marie, S. K. N., et al. (2002). Rod distribution and muscles fibers type modification in the progression of nemaline myopathy. Neuromuscular Disorders. Oxford: Faculdade de Medicina, Universidade de São Paulo. -
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 muscles fibers type modification in the progression of nemaline myopathy. Neuromuscular Disorders. 2002 ; 12( 7-8): 767 res. G.P.6.11.[citado 2026 fev. 22 ] -
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 muscles fibers type modification in the progression of nemaline myopathy. Neuromuscular Disorders. 2002 ; 12( 7-8): 767 res. G.P.6.11.[citado 2026 fev. 22 ] - Estudo imunohistoquímico de proteínas musculares na miopatia nemalínica
- Rod distribution and muscle fiber type modification in the progression of nemaline myopathy
- Rods proteic-constituition and muscle fiber maturation in nemaline myopathy
- Nebulin expression in patients with nemaline myopathy
- 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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