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Artigo de periodico
Association of three diferent mutations in the CLCN1 Gene Modulating the phenotype in a consanguineous family with myotonia congenita (2021)
Souza, Lucas Santos; Calyjur, Priscila; Ribeiro Jr, Antonio Fernando; Gurgel-Giannetti, Juliana; Pavanello, Rita de Cássia Mingroni; Zatz, Mayana ; Vainzof, Mariz
Source: Journal of Molecular Neuroscience. Unidade: IB
Subjects: DOENÇAS NEUROMUSCULARES, MUTAÇÃO GENÉTICA, MIOPATIAS CONGÊNITAS ESTRUTURAIS, DOENÇAS GENÉTICAS, FENÓTIPOS
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ABNT
SOUZA, Lucas Santos et al. Association of three diferent mutations in the CLCN1 Gene Modulating the phenotype in a consanguineous family with myotonia congenita. Journal of Molecular Neuroscience, n. Ja 2021, 2021Tradução . . Disponível em: https://doi.org/10.1007/s12031-020-01785-4. Acesso em: 05 nov. 2024.
APA
Souza, L. S., Calyjur, P., Ribeiro Jr, A. F., Gurgel-Giannetti, J., Pavanello, R. de C. M., Zatz, M., & Vainzof, M. (2021). Association of three diferent mutations in the CLCN1 Gene Modulating the phenotype in a consanguineous family with myotonia congenita. Journal of Molecular Neuroscience, ( Ja 2021). doi:10.1007/s12031-020-01785-4
NLM
Souza LS, Calyjur P, Ribeiro Jr AF, Gurgel-Giannetti J, Pavanello R de CM, Zatz M, Vainzof M. Association of three diferent mutations in the CLCN1 Gene Modulating the phenotype in a consanguineous family with myotonia congenita [Internet]. Journal of Molecular Neuroscience. 2021 ;( Ja 2021):[citado 2024 nov. 05 ] Available from: https://doi.org/10.1007/s12031-020-01785-4
Vancouver
Souza LS, Calyjur P, Ribeiro Jr AF, Gurgel-Giannetti J, Pavanello R de CM, Zatz M, Vainzof M. Association of three diferent mutations in the CLCN1 Gene Modulating the phenotype in a consanguineous family with myotonia congenita [Internet]. Journal of Molecular Neuroscience. 2021 ;( Ja 2021):[citado 2024 nov. 05 ] Available from: https://doi.org/10.1007/s12031-020-01785-4
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
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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: 05 nov. 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 nov. 05 ] 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 nov. 05 ] Available from: https://doi.org/10.1007/s12031-010-9445-7
Artigo de periodico
The gentics of Alzheimer´s Disease in Brazil: 10 years of analysis in a unique population (2009)
Oliveira, João Ricardo Mendes de; Nishimura, Agnes Lumi; Lemos, R. R; Zatz, Mayana
Source: Journal of Molecular Neuroscience. Unidade: IB
Subjects: DOENÇA DE ALZHEIMER, GENÉTICA
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ABNT
OLIVEIRA, João Ricardo Mendes de et al. The gentics of Alzheimer´s Disease in Brazil: 10 years of analysis in a unique population. Journal of Molecular Neuroscience, v. 37, n. 1, p. 74-79, 2009Tradução . . Disponível em: https://doi.org/10.1007/s12031-008-9124-0. Acesso em: 05 nov. 2024.
APA
Oliveira, J. R. M. de, Nishimura, A. L., Lemos, R. R., & Zatz, M. (2009). The gentics of Alzheimer´s Disease in Brazil: 10 years of analysis in a unique population. Journal of Molecular Neuroscience, 37( 1), 74-79. doi:10.1007/s12031-008-9124-0
NLM
Oliveira JRM de, Nishimura AL, Lemos RR, Zatz M. The gentics of Alzheimer´s Disease in Brazil: 10 years of analysis in a unique population [Internet]. Journal of Molecular Neuroscience. 2009 ; 37( 1): 74-79.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1007/s12031-008-9124-0
Vancouver
Oliveira JRM de, Nishimura AL, Lemos RR, Zatz M. The gentics of Alzheimer´s Disease in Brazil: 10 years of analysis in a unique population [Internet]. Journal of Molecular Neuroscience. 2009 ; 37( 1): 74-79.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1007/s12031-008-9124-0
Artigo de periodico
Monoamine oxidase a polymorphism in brazilian patients (2005)
Nishimura, Agnes Lumi; Guindalini, Camila; Oliveira, João Ricardo Mendes de; Nitrini, Ricardo; Bahia, Valéria Santoro; Brito-Marques, Paulo Roberto; Otto, Paulo A ; Zatz, Mayana
Source: Journal of Molecular Neuroscience. Unidades: FM, IB
Subjects: DEMÊNCIA, NEUROLOGIA, POLIMORFISMO
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ABNT
NISHIMURA, Agnes Lumi et al. Monoamine oxidase a polymorphism in brazilian patients. Journal of Molecular Neuroscience, v. 27, p. 213-217, 2005Tradução . . Acesso em: 05 nov. 2024.
APA
Nishimura, A. L., Guindalini, C., Oliveira, J. R. M. de, Nitrini, R., Bahia, V. S., Brito-Marques, P. R., et al. (2005). Monoamine oxidase a polymorphism in brazilian patients. Journal of Molecular Neuroscience, 27, 213-217.
NLM
Nishimura AL, Guindalini C, Oliveira JRM de, Nitrini R, Bahia VS, Brito-Marques PR, Otto PA, Zatz M. Monoamine oxidase a polymorphism in brazilian patients. Journal of Molecular Neuroscience. 2005 ; 27 213-217.[citado 2024 nov. 05 ]
Vancouver
Nishimura AL, Guindalini C, Oliveira JRM de, Nitrini R, Bahia VS, Brito-Marques PR, Otto PA, Zatz M. Monoamine oxidase a polymorphism in brazilian patients. Journal of Molecular Neuroscience. 2005 ; 27 213-217.[citado 2024 nov. 05 ]
Artigo de periodico
Analysis of IL-1'alfa', IL-1'beta', and IL-RA polymorphisms in dysthymia (2004)
Fertuzinhos, Sofia M. M.; Oliveira, João R. Mendes de; Nishimura, Agnes Lumi; Pontual, Deyse; Carvalho, Daniel Resende; Sougey, Everton Botelho; Otto, Paulo A ; Zatz, Mayana
Source: Journal of Molecular Neuroscience. Unidade: IB
Subjects: TRANSTORNOS MENTAIS, TRANSTORNO DISTÍMICO
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ABNT
FERTUZINHOS, Sofia M. M. et al. Analysis of IL-1'alfa', IL-1'beta', and IL-RA polymorphisms in dysthymia. Journal of Molecular Neuroscience, v. 22, n. 3, p. 251-255, 2004Tradução . . Acesso em: 05 nov. 2024.
APA
Fertuzinhos, S. M. M., Oliveira, J. R. M. de, Nishimura, A. L., Pontual, D., Carvalho, D. R., Sougey, E. B., et al. (2004). Analysis of IL-1'alfa', IL-1'beta', and IL-RA polymorphisms in dysthymia. Journal of Molecular Neuroscience, 22( 3), 251-255.
NLM
Fertuzinhos SMM, Oliveira JRM de, Nishimura AL, Pontual D, Carvalho DR, Sougey EB, Otto PA, Zatz M. Analysis of IL-1'alfa', IL-1'beta', and IL-RA polymorphisms in dysthymia. Journal of Molecular Neuroscience. 2004 ; 22( 3): 251-255.[citado 2024 nov. 05 ]
Vancouver
Fertuzinhos SMM, Oliveira JRM de, Nishimura AL, Pontual D, Carvalho DR, Sougey EB, Otto PA, Zatz M. Analysis of IL-1'alfa', IL-1'beta', and IL-RA polymorphisms in dysthymia. Journal of Molecular Neuroscience. 2004 ; 22( 3): 251-255.[citado 2024 nov. 05 ]
Artigo de periodico
Lack of association between the brain-derived neurotrophin factor (C-270T) polymorphism and late-onset Alzheimers disease (LOAD) in Brazilian patients (2004)
Nishimura, Agnes Lumi; Oliveira, João Ricardo Mendes de; Nitrini, Ricardo; Bahia, Valéria Santoro; Brito-Marques, Paulo Roberto; Otto, Paulo A ; Zatz, Mayana
Source: Journal of Molecular Neuroscience. Unidades: FM, IB
Subjects: DOENÇA DE ALZHEIMER, POLIMORFISMO, APOLIPOPROTEÍNAS, BRASIL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NISHIMURA, Agnes Lumi et al. Lack of association between the brain-derived neurotrophin factor (C-270T) polymorphism and late-onset Alzheimers disease (LOAD) in Brazilian patients. Journal of Molecular Neuroscience, v. 22, p. 257-260, 2004Tradução . . Acesso em: 05 nov. 2024.
APA
Nishimura, A. L., Oliveira, J. R. M. de, Nitrini, R., Bahia, V. S., Brito-Marques, P. R., Otto, P. A., & Zatz, M. (2004). Lack of association between the brain-derived neurotrophin factor (C-270T) polymorphism and late-onset Alzheimers disease (LOAD) in Brazilian patients. Journal of Molecular Neuroscience, 22, 257-260.
NLM
Nishimura AL, Oliveira JRM de, Nitrini R, Bahia VS, Brito-Marques PR, Otto PA, Zatz M. Lack of association between the brain-derived neurotrophin factor (C-270T) polymorphism and late-onset Alzheimers disease (LOAD) in Brazilian patients. Journal of Molecular Neuroscience. 2004 ; 22 257-260.[citado 2024 nov. 05 ]
Vancouver
Nishimura AL, Oliveira JRM de, Nitrini R, Bahia VS, Brito-Marques PR, Otto PA, Zatz M. Lack of association between the brain-derived neurotrophin factor (C-270T) polymorphism and late-onset Alzheimers disease (LOAD) in Brazilian patients. Journal of Molecular Neuroscience. 2004 ; 22 257-260.[citado 2024 nov. 05 ]
Artigo de periodico
Deficiency of muscle 'alfa'-Actinin-3 is compatible with high muscle performance (2003)
Zanoteli, Edmar; Lotuffo, Renato M.; Oliveira, Acary Souza Bulle; Beggs, Alan H.; Canovas, Marta; Zatz, Mayana ; Vainzof, Mariz
Source: Journal of Molecular Neuroscience. Unidade: IB
Subjects: MÚSCULOS, FIBRAS, CORRIDAS
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ABNT
ZANOTELI, Edmar et al. Deficiency of muscle 'alfa'-Actinin-3 is compatible with high muscle performance. Journal of Molecular Neuroscience, v. 20, n. 1, p. 39-42, 2003Tradução . . Acesso em: 05 nov. 2024.
APA
Zanoteli, E., Lotuffo, R. M., Oliveira, A. S. B., Beggs, A. H., Canovas, M., Zatz, M., & Vainzof, M. (2003). Deficiency of muscle 'alfa'-Actinin-3 is compatible with high muscle performance. Journal of Molecular Neuroscience, 20( 1), 39-42.
NLM
Zanoteli E, Lotuffo RM, Oliveira ASB, Beggs AH, Canovas M, Zatz M, Vainzof M. Deficiency of muscle 'alfa'-Actinin-3 is compatible with high muscle performance. Journal of Molecular Neuroscience. 2003 ; 20( 1): 39-42.[citado 2024 nov. 05 ]
Vancouver
Zanoteli E, Lotuffo RM, Oliveira ASB, Beggs AH, Canovas M, Zatz M, Vainzof M. Deficiency of muscle 'alfa'-Actinin-3 is compatible with high muscle performance. Journal of Molecular Neuroscience. 2003 ; 20( 1): 39-42.[citado 2024 nov. 05 ]
Artigo de periodico
Calpainopathy: how broad is the spectrum of clinical variability? (2003)
Starling, Alessandra; Paula, Flavia de; Silva, Helga Cristina Almeida da; Vainzof, Mariz ; Zatz, Mayana
Source: Journal of Molecular Neuroscience. Unidade: IB
Subjects: DISTROFIA MUSCULAR (HUMANO), MUTAÇÃO GENÉTICA
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ABNT
STARLING, Alessandra et al. Calpainopathy: how broad is the spectrum of clinical variability?. Journal of Molecular Neuroscience, v. 21, n. 3, p. 233-236, 2003Tradução . . Acesso em: 05 nov. 2024.
APA
Starling, A., Paula, F. de, Silva, H. C. A. da, Vainzof, M., & Zatz, M. (2003). Calpainopathy: how broad is the spectrum of clinical variability? Journal of Molecular Neuroscience, 21( 3), 233-236.
NLM
Starling A, Paula F de, Silva HCA da, Vainzof M, Zatz M. Calpainopathy: how broad is the spectrum of clinical variability? Journal of Molecular Neuroscience. 2003 ; 21( 3): 233-236.[citado 2024 nov. 05 ]
Vancouver
Starling A, Paula F de, Silva HCA da, Vainzof M, Zatz M. Calpainopathy: how broad is the spectrum of clinical variability? Journal of Molecular Neuroscience. 2003 ; 21( 3): 233-236.[citado 2024 nov. 05 ]
Artigo de periodico
Dysferlin Protein Analysis in Limb-Girdle Muscular Dystrophies (2001)
Vainzof, Mariz ; Anderson, Louise V. B ; McNally, Elizabeth M ; Davis, Dawn B ; Faulkner, Georgine ; Valle, Giorgio ; Moreira, Eloisa S; Pavanello, Rita C M; Passos-Bueno, Maria Rita ; Zatz, Mayana
Source: Journal of Molecular Neuroscience. Unidade: IB
Subjects: GENÉTICA MÉDICA, DISTROFIA MUSCULAR, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VAINZOF, Mariz et al. Dysferlin Protein Analysis in Limb-Girdle Muscular Dystrophies. Journal of Molecular Neuroscience, v. 17, n. 1, p. 71-80, 2001Tradução . . Disponível em: https://doi.org/10.1385/JMN:17:1:71. Acesso em: 05 nov. 2024.
APA
Vainzof, M., Anderson, L. V. B., McNally, E. M., Davis, D. B., Faulkner, G., Valle, G., et al. (2001). Dysferlin Protein Analysis in Limb-Girdle Muscular Dystrophies. Journal of Molecular Neuroscience, 17( 1), 71-80. doi:10.1385/JMN:17:1:71
NLM
Vainzof M, Anderson LVB, McNally EM, Davis DB, Faulkner G, Valle G, Moreira ES, Pavanello RCM, Passos-Bueno MR, Zatz M. Dysferlin Protein Analysis in Limb-Girdle Muscular Dystrophies [Internet]. Journal of Molecular Neuroscience. 2001 ; 17( 1): 71-80.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1385/JMN:17:1:71
Vancouver
Vainzof M, Anderson LVB, McNally EM, Davis DB, Faulkner G, Valle G, Moreira ES, Pavanello RCM, Passos-Bueno MR, Zatz M. Dysferlin Protein Analysis in Limb-Girdle Muscular Dystrophies [Internet]. Journal of Molecular Neuroscience. 2001 ; 17( 1): 71-80.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1385/JMN:17:1:71

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