Nebulin expression in patients with nemaline myopathy (1999)
- Authors:
- USP affiliated authors: REED, UMBERTINA CONTI - FM ; MARIE, SUELY KAZUE NAGAHASHI - FM ; ZATZ, MAYANA - IB
- Unidades: FM; IB
- Assunto: NEUROLOGIA
- Language: Inglês
- Imprenta:
- Publisher place: Estados Unidos
- Date published: 1999
- Source:
- Título: Neuromuscular Disorders
- Volume/Número/Paginação/Ano: v. 09, n. 06-07, p. 513, res. G.P.5.2, 1999
- Conference titles: International Congress of the World Muscle Society
-
ABNT
GURGEL, J. E. P et al. Nebulin expression in patients with nemaline myopathy. Neuromuscular Disorders. Estados Unidos: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 15 fev. 2026. , 1999 -
APA
Gurgel, J. E. P., Reed, U. C., Marie, S. K. N., Carvalho, M., Zanoteli, E., Fireman, M. A. T., et al. (1999). Nebulin expression in patients with nemaline myopathy. Neuromuscular Disorders. Estados Unidos: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Gurgel JEP, Reed UC, Marie SKN, Carvalho M, Zanoteli E, Fireman MAT, Oliveira ASB, Zatz M, Vainzof M. Nebulin expression in patients with nemaline myopathy. Neuromuscular Disorders. 1999 ; 09( 06-07): 513.[citado 2026 fev. 15 ] -
Vancouver
Gurgel JEP, Reed UC, Marie SKN, Carvalho M, Zanoteli E, Fireman MAT, Oliveira ASB, Zatz M, Vainzof M. Nebulin expression in patients with nemaline myopathy. Neuromuscular Disorders. 1999 ; 09( 06-07): 513.[citado 2026 fev. 15 ] - Rods proteic-constituition and muscle fiber maturation in nemaline myopathy
- Nemaline myopathy (NM) 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
- Phenotypic and immunohistochemical characterization of sarcoglycanopathies
- MHC class 1 as an additional marker to the course of juvenille dermatomyositis
- Distrofia Muscular Congênita Como Causa de Fraqueza Cervical
- The correlation between upper limbs and trunk involvement in patients with duchenne muscular dystrophy and the perfomance in scholar as well as daily activities
- Perfil Funcional de Pacientes com Distrofia Muscular de Duchenne
- Deletions of study of dystrophin gene in Duchenne and Becker muscular dystrophy
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
