A patient with ataxia with oculomotor apraxia type 1 and slow conduction velocities (2017)
- Authors:
- USP affiliated authors: BARREIRA, AMILTON ANTUNES - FMRP ; MARQUES JÚNIOR, WILSON - FMRP
- Unidade: FMRP
- Subjects: ATAXIA; ATROFIA DE MÚLTIPLOS SISTEMAS; DOENÇAS DO SISTEMA NERVOSO
- Language: Inglês
- Imprenta:
- Source:
- Título: Abstracts
- Conference titles: Annual Meeting of Peripheral Nerve Society - PNS
-
ABNT
TOMASELLI, P. J. et al. A patient with ataxia with oculomotor apraxia type 1 and slow conduction velocities. 2017, Anais.. Barcelona: PNS, 2017. . Acesso em: 11 mar. 2026. -
APA
Tomaselli, P. J., Lourenço, C. M., Cintra, V. P., Barreira, A. A., & Marques Júnior, W. (2017). A patient with ataxia with oculomotor apraxia type 1 and slow conduction velocities. In Abstracts. Barcelona: PNS. -
NLM
Tomaselli PJ, Lourenço CM, Cintra VP, Barreira AA, Marques Júnior W. A patient with ataxia with oculomotor apraxia type 1 and slow conduction velocities. Abstracts. 2017 ;[citado 2026 mar. 11 ] -
Vancouver
Tomaselli PJ, Lourenço CM, Cintra VP, Barreira AA, Marques Júnior W. A patient with ataxia with oculomotor apraxia type 1 and slow conduction velocities. Abstracts. 2017 ;[citado 2026 mar. 11 ] - Concurrent multiple sclerosis and amyotrophic lateral sclerosis
- Perdas sensitivas no tronco em pacientes com neuropatias desmielizantes
- Imunoterapia em sgb, mg, pidc e em v. Ciclofosfomida ciclosporina / combinacao procedimentos e b-interflon
- Imunoterapia na mg, sgb, pidc e esclerose multipla i. Plasmaferese
- Estudo das neuropatias periféricas no Estado de São Paulo de 1939 a 1985
- Estudo neurofisiologico em neuropatia apos intoxicacao com organo fosforado
- Imunoglobina humana endovenosa em altas doses (igiv) na sindrome de guillain barre (sgb)
- Hereditary neuropathy with liability to pressure palsies (HNPP): differential diagnosis with aquired neuropathies
- 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
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
