A clinical phenotype of chronic inflammatory demyelinating polyneuropathy (CIDP) associated with persistent conduction block (2006)
- Authors:
- USP affiliated authors: MARQUES JÚNIOR, WILSON - FMRP ; BARREIRA, AMILTON ANTUNES - FMRP
- Unidade: FMRP
- Assunto: NEUROLOGIA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Arquivos de Neuro-Psiquiatria
- Volume/Número/Paginação/Ano: v. 64, supl. 1, p. 109, res. P-350, 2006
- Conference titles: Congresso Brasileiro de Neurologia
-
ABNT
RESENDE, C. C. et al. A clinical phenotype of chronic inflammatory demyelinating polyneuropathy (CIDP) associated with persistent conduction block. Arquivos de Neuro-Psiquiatria. São Paulo: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 24 mar. 2023. , 2006 -
APA
Resende, C. C., Barreira, A. A., Nascimento, O., Marques Júnior, W., & Flauzino, J. A. (2006). A clinical phenotype of chronic inflammatory demyelinating polyneuropathy (CIDP) associated with persistent conduction block. Arquivos de Neuro-Psiquiatria. São Paulo: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. -
NLM
Resende CC, Barreira AA, Nascimento O, Marques Júnior W, Flauzino JA. A clinical phenotype of chronic inflammatory demyelinating polyneuropathy (CIDP) associated with persistent conduction block. Arquivos de Neuro-Psiquiatria. 2006 ; 64 109.[citado 2023 mar. 24 ] -
Vancouver
Resende CC, Barreira AA, Nascimento O, Marques Júnior W, Flauzino JA. A clinical phenotype of chronic inflammatory demyelinating polyneuropathy (CIDP) associated with persistent conduction block. Arquivos de Neuro-Psiquiatria. 2006 ; 64 109.[citado 2023 mar. 24 ] - Clinical manifestations of patients with the hereditary neuropathy with liability to pressure palsies (HNPP) and deletion of 17P11.2 chromossome
- Phenotypic characterization of late-onset TTR met 30 familiar amyloid polyneuropathy
- A descriptive study of a Brazilian population with early onset chronic peripheral polyneuropathy
- A mild and unusual CMT compound phenotype due to the presence of two mutations in pmP22 gene: 17p duplication and Ser72Leuc
- The one limb multineuropathy of neural leprosy
- Coexistence of CMT1A and diabetes mellitus in a young woman with a severe and progressive neuropathy and respiratory insufficiency. [Carta]
- Concurrent multiple sclerosis and amyotrophic lateral sclerosis
- A MPZ R98C CMT patient presenting a fluctuating neuropathy susceptible to treatment
- A patient with ataxia with oculomotor apraxia type 1 and slow conduction velocities
- A MPZ R98C CMT patient presenting a fluctuating neuropathy susceptible to treatment
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas