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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: 11 jun. 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 jun. 11 ] 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 jun. 11 ] Available from: https://doi.org/10.4103/1673-5374.303030
Artigo de periodico
DNA methylation fingerprint of monozygotic twins and their singleton sibling with intellectual disability carrying a novel KDM5C mutation (2020)
Guerra, João V.S; Oliveira-Santos, José; Oliveira, Danyllo F ; Leal, Gabriela F.; Oliveira, João Ricardo M.; Costa, Sílvia S; Krepischi, Ana Cristina Victorino ; Vianna-Morgante, Angela M ; Maschietto, Mariana
Source: European Journal of Medical Genetics. Unidade: IB
Subjects: GENÉTICA MÉDICA, PESSOAS COM DEFICIÊNCIA INTELECTUAL, METILAÇÃO DE DNA, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUERRA, João V.S et al. DNA methylation fingerprint of monozygotic twins and their singleton sibling with intellectual disability carrying a novel KDM5C mutation. European Journal of Medical Genetics, v. 63, n. 3, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.ejmg.2019.103737. Acesso em: 11 jun. 2024.
APA
Guerra, J. V. S., Oliveira-Santos, J., Oliveira, D. F., Leal, G. F., Oliveira, J. R. M., Costa, S. S., et al. (2020). DNA methylation fingerprint of monozygotic twins and their singleton sibling with intellectual disability carrying a novel KDM5C mutation. European Journal of Medical Genetics, 63( 3). doi:10.1016/j.ejmg.2019.103737
NLM
Guerra JVS, Oliveira-Santos J, Oliveira DF, Leal GF, Oliveira JRM, Costa SS, Krepischi ACV, Vianna-Morgante AM, Maschietto M. DNA methylation fingerprint of monozygotic twins and their singleton sibling with intellectual disability carrying a novel KDM5C mutation [Internet]. European Journal of Medical Genetics. 2020 ; 63( 3):[citado 2024 jun. 11 ] Available from: https://doi.org/10.1016/j.ejmg.2019.103737
Vancouver
Guerra JVS, Oliveira-Santos J, Oliveira DF, Leal GF, Oliveira JRM, Costa SS, Krepischi ACV, Vianna-Morgante AM, Maschietto M. DNA methylation fingerprint of monozygotic twins and their singleton sibling with intellectual disability carrying a novel KDM5C mutation [Internet]. European Journal of Medical Genetics. 2020 ; 63( 3):[citado 2024 jun. 11 ] Available from: https://doi.org/10.1016/j.ejmg.2019.103737
Artigo de periodico
Population and computational analysis of the MGEA6 P521A variation as a risk factor for familial Idiopathic Basal Ganglia Calcification (Fahr’s Disease) (2011)
Lemos, Roberta R.; Oliveira, Danyllo F; Zatz, Mayana ; Oliveira, João R. M
Source: Journal of Molecular Neuroscience. Unidade: IB
Subjects: DOENÇAS GENÉTICAS, POLIMORFISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LEMOS, Roberta R. et al. Population and computational analysis of the MGEA6 P521A variation as a risk factor for familial Idiopathic Basal Ganglia Calcification (Fahr’s Disease). Journal of Molecular Neuroscience, v. 43, n. 3, p. 333-336, 2011Tradução . . Disponível em: https://doi.org/10.1007/s12031-010-9445-7. Acesso em: 11 jun. 2024.
APA
Lemos, R. R., Oliveira, D. F., Zatz, M., & Oliveira, J. R. M. (2011). Population and computational analysis of the MGEA6 P521A variation as a risk factor for familial Idiopathic Basal Ganglia Calcification (Fahr’s Disease). Journal of Molecular Neuroscience, 43( 3), 333-336. doi:10.1007/s12031-010-9445-7
NLM
Lemos RR, Oliveira DF, Zatz M, Oliveira JRM. Population and computational analysis of the MGEA6 P521A variation as a risk factor for familial Idiopathic Basal Ganglia Calcification (Fahr’s Disease) [Internet]. Journal of Molecular Neuroscience. 2011 ; 43( 3): 333-336.[citado 2024 jun. 11 ] Available from: https://doi.org/10.1007/s12031-010-9445-7
Vancouver
Lemos RR, Oliveira DF, Zatz M, Oliveira JRM. Population and computational analysis of the MGEA6 P521A variation as a risk factor for familial Idiopathic Basal Ganglia Calcification (Fahr’s Disease) [Internet]. Journal of Molecular Neuroscience. 2011 ; 43( 3): 333-336.[citado 2024 jun. 11 ] Available from: https://doi.org/10.1007/s12031-010-9445-7

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