A MPZ R98C CMT patient presenting a fluctuating neuropathy susceptible to treatment (2017)
- Authors:
- USP affiliated authors: BARREIRA, AMILTON ANTUNES - FMRP ; MARQUES JÚNIOR, WILSON - FMRP
- Unidade: FMRP
- Assunto: DOENÇAS DO SISTEMA NERVOSO
- Language: Inglês
- Imprenta:
- Source:
- Título: Abstracts
- Conference titles: Annual Meeting of Peripheral Nerve Society - PNS
-
ABNT
GERMANO, C. S. B. et al. A MPZ R98C CMT patient presenting a fluctuating neuropathy susceptible to treatment. 2017, Anais.. Barcelona: PNS, 2017. . Acesso em: 30 dez. 2025. -
APA
Germano, C. S. B., Onofre, P. T. B. N., Bordini, E. C., Gouvea, S., Barreira, A. A., & Marques Júnior, W. (2017). A MPZ R98C CMT patient presenting a fluctuating neuropathy susceptible to treatment. In Abstracts. Barcelona: PNS. -
NLM
Germano CSB, Onofre PTBN, Bordini EC, Gouvea S, Barreira AA, Marques Júnior W. A MPZ R98C CMT patient presenting a fluctuating neuropathy susceptible to treatment. Abstracts. 2017 ;[citado 2025 dez. 30 ] -
Vancouver
Germano CSB, Onofre PTBN, Bordini EC, Gouvea S, Barreira AA, Marques Júnior W. A MPZ R98C CMT patient presenting a fluctuating neuropathy susceptible to treatment. Abstracts. 2017 ;[citado 2025 dez. 30 ] - Polineuropatia desmielinizante associada a gamopatia monoclonal por IGA (IGAP) com comprometimento sensitivo extenso incluindo o eixo corporal
- Polineuropatia desmielinizante sensitiva
- Resposta simpatica cutanea (rsc) na mielopatia associada ao htlv-i / paraparesia espastica tropical
- Opcoes de tratamento na polineuropatia inflamatoria cronica desmielinizante
- Chronic inflammatory demyelinating polyneuropathy in diabetics (CIDPD) and chronic polyneuropathy (CIDP)
- Manifestações clínicas atípicas na neuropatia hereditária com sensibilidade à compressão
- 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 patient with ataxia with oculomotor apraxia type 1 and slow conduction velocities
- A descriptive study of a Brazilian population with early onset chronic peripheral polyneuropathy
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
