An evolutionary study of 72 children with Guillain-Barré (2001)
- Authors:
- USP affiliated authors: BARREIRA, AMILTON ANTUNES - FMRP ; FUNAYAMA, CAROLINA ARAUJO RODRIGUES - FMRP ; MARQUES JÚNIOR, WILSON - FMRP
- School: FMRP
- Subjects: DOENÇAS DO SISTEMA NERVOSO PERIFÉRICO; CRIANÇAS
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Journal of the Peripheral Nervous System
- Volume/Número/Paginação/Ano: v. 6, n. 3, p. 130-131, 2001
- Conference title: Meeting of the Peripheral Nerve Society
-
ABNT
BARREIRA, Amilton Antunes; ALVES, D. M.; FUNAYAMA, Carolina Araujo Rodrigues; MARQUES JÚNIOR, Wilson. An evolutionary study of 72 children with Guillain-Barré. Journal of the Peripheral Nervous System[S.l: s.n.], 2001. -
APA
Barreira, A. A., Alves, D. M., Funayama, C. A. R., & Marques Júnior, W. (2001). An evolutionary study of 72 children with Guillain-Barré. Journal of the Peripheral Nervous System. New York. -
NLM
Barreira AA, Alves DM, Funayama CAR, Marques Júnior W. An evolutionary study of 72 children with Guillain-Barré. Journal of the Peripheral Nervous System. 2001 ; 6( 3): 130-131. -
Vancouver
Barreira AA, Alves DM, Funayama CAR, Marques Júnior W. An evolutionary study of 72 children with Guillain-Barré. Journal of the Peripheral Nervous System. 2001 ; 6( 3): 130-131. - Coexistence of two chronic neuropathies in a young child: Charcot-Marie-Tooth disease type 1A and chronic inflammatory demyelinating polyneuropathy
- Concomitance of an inherited and an acquired demyelinating neuropathy in a young girl
- Maior susceptibilidade dos sistemas piramidal e cerebelar à disfunção da ATPase mitocondrial em uma família com a mutação T8993G no mtDNA
- Síndrome de Guillain-Barré (SGB) em crianças
- An evolutionary study of 72 children with guillain-barré syndrome
- Tyrosinemia type II (Richner-Hanhart syndrome): a rare disease with neurologic manifestations
- Correlação entre ENMG e biopsia em pacientes com síndrome da criança hipotônica
- Clinical and electrophysiological characteristics of children and adolescents with chronic peripheral neuropathy in a south american tertiary neuromuscular center
- A clinical phenotype of chronic inflammatory demyelinating polyneuropathy (CIDP) associated with persistent conduction block
- Autologous stem cell transplantation (ASCT) in patient with a chronic demyelinating neuropathy and persistent conduction block
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