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Filtros : "MUTAÇÃO GENÉTICA" "Financiamento INCT" Removidos: "Gastroenterologia Clínica" "3Laboratory of Cell Structure and Dynamics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, 20892, USA" Limpar

Filtros

USP affiliated authors
- almeida, sergio verjovski de (1)
- figueiredo, fernanda barbosa (1)
- giuliatti, silvana (1)
- hallak, jaime eduardo cecilio (1)
- marques júnior, wilson (1)

Date published
- 2021 (~2)
Subjects
- mutação genética (2)
- células-tronco (1)
- doenças degenerativas (1)
- doenças do sistema nervoso (1)
- doenças neurodegenerativas (1)

Artigo de periodico
Phenotypic heterogeneity in amyotrophic lateral sclerosis type 8 and modifying mechanisms of neurodegeneration (2021)
Oliveira, Danyllo F ; Verjovski-Almeida, Sergio ; Zatz, Mayana
Source: Neural Regeneration Research. Unidades: IQ, IB
Subjects: ESCLEROSE AMIOTRÓFICA LATERAL, DOENÇAS NEURODEGENERATIVAS, MUTAÇÃO GENÉTICA, CÉLULAS-TRONCO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OLIVEIRA, Danyllo F e VERJOVSKI-ALMEIDA, Sergio e ZATZ, Mayana. Phenotypic heterogeneity in amyotrophic lateral sclerosis type 8 and modifying mechanisms of neurodegeneration. Neural Regeneration Research, v. 16, n. 9, p. 1776-1778, 2021Tradução . . Disponível em: https://doi.org/10.4103/1673-5374.303030. Acesso em: 12 nov. 2024.
APA
Oliveira, D. F., Verjovski-Almeida, S., & Zatz, M. (2021). Phenotypic heterogeneity in amyotrophic lateral sclerosis type 8 and modifying mechanisms of neurodegeneration. Neural Regeneration Research, 16( 9), 1776-1778. doi:10.4103/1673-5374.303030
NLM
Oliveira DF, Verjovski-Almeida S, Zatz M. Phenotypic heterogeneity in amyotrophic lateral sclerosis type 8 and modifying mechanisms of neurodegeneration [Internet]. Neural Regeneration Research. 2021 ; 16( 9): 1776-1778.[citado 2024 nov. 12 ] Available from: https://doi.org/10.4103/1673-5374.303030
Vancouver
Oliveira DF, Verjovski-Almeida S, Zatz M. Phenotypic heterogeneity in amyotrophic lateral sclerosis type 8 and modifying mechanisms of neurodegeneration [Internet]. Neural Regeneration Research. 2021 ; 16( 9): 1776-1778.[citado 2024 nov. 12 ] Available from: https://doi.org/10.4103/1673-5374.303030
Artigo de periodico
GDAP1 mutations are frequent among Brazilian patients with autosomal recessive axonal Charcot-Marie-Tooth disease (2021)
Figueiredo, Fernanda Barbosa ; Silva Junior, Wilson Araújo da ; Giuliatti, Silvana ; Tomaselli, Pedro José; Lourenço, Charles Marques; Gouvêa, Silmara Paula; Covaleski, Anna Paula Paranhos Miranda; Hallak, Jaime Eduardo Cecilio ; Marques Júnior, Wilson
Source: Neuromuscular Disorders. Unidade: FMRP
Subjects: DOENÇAS DO SISTEMA NERVOSO, DOENÇAS DEGENERATIVAS, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FIGUEIREDO, Fernanda Barbosa et al. GDAP1 mutations are frequent among Brazilian patients with autosomal recessive axonal Charcot-Marie-Tooth disease. Neuromuscular Disorders, v. 31, n. 6, p. 505-511, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.nmd.2021.03.005. Acesso em: 12 nov. 2024.
APA
Figueiredo, F. B., Silva Junior, W. A. da, Giuliatti, S., Tomaselli, P. J., Lourenço, C. M., Gouvêa, S. P., et al. (2021). GDAP1 mutations are frequent among Brazilian patients with autosomal recessive axonal Charcot-Marie-Tooth disease. Neuromuscular Disorders, 31( 6), 505-511. doi:10.1016/j.nmd.2021.03.005
NLM
Figueiredo FB, Silva Junior WA da, Giuliatti S, Tomaselli PJ, Lourenço CM, Gouvêa SP, Covaleski APPM, Hallak JEC, Marques Júnior W. GDAP1 mutations are frequent among Brazilian patients with autosomal recessive axonal Charcot-Marie-Tooth disease [Internet]. Neuromuscular Disorders. 2021 ; 31( 6): 505-511.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1016/j.nmd.2021.03.005
Vancouver
Figueiredo FB, Silva Junior WA da, Giuliatti S, Tomaselli PJ, Lourenço CM, Gouvêa SP, Covaleski APPM, Hallak JEC, Marques Júnior W. GDAP1 mutations are frequent among Brazilian patients with autosomal recessive axonal Charcot-Marie-Tooth disease [Internet]. Neuromuscular Disorders. 2021 ; 31( 6): 505-511.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1016/j.nmd.2021.03.005

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