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Artigo de periodico
Lipidomic analysis identified potential predictive biomarkers of statin response in subjects with Familial hypercholesterolemia (2023)
Cerda, Alvaro; Bortolin, Raul Hernandes ; Yoshinaga, Marcos Yukio ; Freitas, Renata Caroline Costa de ; Hernandez, Carolina Dagli; Borges, Jessica Bassani; Oliveira, Victor Fernandes de ; Gonçalves, Rodrigo Marques; Faludi, André Arpad; Bastos, Gisele Medeiros ; Hirata, Rosario Dominguez Crespo ; Hirata, Mario Hiroyuki
Fonte: Chemistry and Physics of Lipids. Unidades: FCF, ICB
Assuntos: BIOMARCADORES, ESTATINAS, HIPERCOLESTEROLEMIA
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ABNT
CERDA, Alvaro et al. Lipidomic analysis identified potential predictive biomarkers of statin response in subjects with Familial hypercholesterolemia. Chemistry and Physics of Lipids, v. 257, p. 1-9 art. 105348, 2023Tradução . . Disponível em: https://dx.doi.org/10.1016/j.chemphyslip.2023.105348. Acesso em: 02 jul. 2024.
APA
Cerda, A., Bortolin, R. H., Yoshinaga, M. Y., Freitas, R. C. C. de, Hernandez, C. D., Borges, J. B., et al. (2023). Lipidomic analysis identified potential predictive biomarkers of statin response in subjects with Familial hypercholesterolemia. Chemistry and Physics of Lipids, 257, 1-9 art. 105348. doi:10.1016/j.chemphyslip.2023.105348
NLM
Cerda A, Bortolin RH, Yoshinaga MY, Freitas RCC de, Hernandez CD, Borges JB, Oliveira VF de, Gonçalves RM, Faludi AA, Bastos GM, Hirata RDC, Hirata MH. Lipidomic analysis identified potential predictive biomarkers of statin response in subjects with Familial hypercholesterolemia [Internet]. Chemistry and Physics of Lipids. 2023 ; 257 1-9 art. 105348.[citado 2024 jul. 02 ] Available from: https://dx.doi.org/10.1016/j.chemphyslip.2023.105348
Vancouver
Cerda A, Bortolin RH, Yoshinaga MY, Freitas RCC de, Hernandez CD, Borges JB, Oliveira VF de, Gonçalves RM, Faludi AA, Bastos GM, Hirata RDC, Hirata MH. Lipidomic analysis identified potential predictive biomarkers of statin response in subjects with Familial hypercholesterolemia [Internet]. Chemistry and Physics of Lipids. 2023 ; 257 1-9 art. 105348.[citado 2024 jul. 02 ] Available from: https://dx.doi.org/10.1016/j.chemphyslip.2023.105348
Artigo de periodico
Association of variants in MYH7, MYBPC3 and TNNT2 with sudden cardiac death-related risk factors in Brazilian patients with hypertrophic cardiomyopathy (2021)
Mori, Augusto Akira ; Castro, Lara Reinel de; Bortolin, Raul Hernandes ; Bastos, Gisele Medeiros; Oliveira, Victor Fernandes de ; Ferreira, Glaucio Monteiro ; Hirata, Thiago Dominguez Crespo ; Fajardo, Cristina Moreno ; Sampaio, Marcelo Ferraz; Moreira, Dalmo Antonio Ribeiro ; Mateos, José Carlos Pachon; Correia, Edileide de Barros; Sousa, Amanda Guerra de Moraes Rego ; Brion, Maria ; Carracedo, Angel ; Hirata, Rosario Dominguez Crespo ; Hirata, Mario Hiroyuki
Fonte: Forensic Science International. Unidades: FCF, IDPC
Assuntos: MORTE SÚBITA, HIPERTROFIA VENTRICULAR ESQUERDA, FATORES DE RISCO
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ABNT
MORI, Augusto Akira et al. Association of variants in MYH7, MYBPC3 and TNNT2 with sudden cardiac death-related risk factors in Brazilian patients with hypertrophic cardiomyopathy. Forensic Science International, v. 52, p. 1-10 art. 102478, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.fsigen.2021.102478. Acesso em: 02 jul. 2024.
APA
Mori, A. A., Castro, L. R. de, Bortolin, R. H., Bastos, G. M., Oliveira, V. F. de, Ferreira, G. M., et al. (2021). Association of variants in MYH7, MYBPC3 and TNNT2 with sudden cardiac death-related risk factors in Brazilian patients with hypertrophic cardiomyopathy. Forensic Science International, 52, 1-10 art. 102478. doi:10.1016/j.fsigen.2021.102478
NLM
Mori AA, Castro LR de, Bortolin RH, Bastos GM, Oliveira VF de, Ferreira GM, Hirata TDC, Fajardo CM, Sampaio MF, Moreira DAR, Mateos JCP, Correia E de B, Sousa AG de MR, Brion M, Carracedo A, Hirata RDC, Hirata MH. Association of variants in MYH7, MYBPC3 and TNNT2 with sudden cardiac death-related risk factors in Brazilian patients with hypertrophic cardiomyopathy [Internet]. Forensic Science International. 2021 ; 52 1-10 art. 102478.[citado 2024 jul. 02 ] Available from: https://doi.org/10.1016/j.fsigen.2021.102478
Vancouver
Mori AA, Castro LR de, Bortolin RH, Bastos GM, Oliveira VF de, Ferreira GM, Hirata TDC, Fajardo CM, Sampaio MF, Moreira DAR, Mateos JCP, Correia E de B, Sousa AG de MR, Brion M, Carracedo A, Hirata RDC, Hirata MH. Association of variants in MYH7, MYBPC3 and TNNT2 with sudden cardiac death-related risk factors in Brazilian patients with hypertrophic cardiomyopathy [Internet]. Forensic Science International. 2021 ; 52 1-10 art. 102478.[citado 2024 jul. 02 ] Available from: https://doi.org/10.1016/j.fsigen.2021.102478
Artigo de periodico
SNPs from BCHE and DRD3 genes associated to cocaine abuse amongst violent individuals from Sao Paulo, Brazil (2020)
Pego, A. M. F; Leyton, Vilma ; Miziara, Ivan Dieb; Bortolin, Raul Hernandes ; Freitas, R. C. C; Hirata, Mario Hiroyuki ; Tomaz, Paulo Roberto Xavier; Santos, João; Santos, Paulo Caleb Junior Lima; Yonamine, Maurício
Fonte: Forensic Science International. Unidades: FM, FCF
Assuntos: DROGA (VÍCIO), COCAÍNA
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ABNT
PEGO, A. M. F et al. SNPs from BCHE and DRD3 genes associated to cocaine abuse amongst violent individuals from Sao Paulo, Brazil. Forensic Science International, v. 317, p. 1-9 art. 110511, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.forsciint.2020.110511. Acesso em: 02 jul. 2024.
APA
Pego, A. M. F., Leyton, V., Miziara, I. D., Bortolin, R. H., Freitas, R. C. C., Hirata, M. H., et al. (2020). SNPs from BCHE and DRD3 genes associated to cocaine abuse amongst violent individuals from Sao Paulo, Brazil. Forensic Science International, 317, 1-9 art. 110511. doi:10.1016/j.forsciint.2020.110511
NLM
Pego AMF, Leyton V, Miziara ID, Bortolin RH, Freitas RCC, Hirata MH, Tomaz PRX, Santos J, Santos PCJL, Yonamine M. SNPs from BCHE and DRD3 genes associated to cocaine abuse amongst violent individuals from Sao Paulo, Brazil [Internet]. Forensic Science International. 2020 ; 317 1-9 art. 110511.[citado 2024 jul. 02 ] Available from: https://doi.org/10.1016/j.forsciint.2020.110511
Vancouver
Pego AMF, Leyton V, Miziara ID, Bortolin RH, Freitas RCC, Hirata MH, Tomaz PRX, Santos J, Santos PCJL, Yonamine M. SNPs from BCHE and DRD3 genes associated to cocaine abuse amongst violent individuals from Sao Paulo, Brazil [Internet]. Forensic Science International. 2020 ; 317 1-9 art. 110511.[citado 2024 jul. 02 ] Available from: https://doi.org/10.1016/j.forsciint.2020.110511
Artigo de periodico
Genetic susceptibility in pharmacodynamic and pharmacokinetic pathways underlying drug-induced arrhythmia and sudden unexplained deaths (2019)
Matilla, Marina Martinez; Verea, Alejandro J. Blanco; Santori, Montserrat; Bermejo, Juan Ansede; Luis, Eva Ramos; Gil, Rocio; Bermejo, Ana María; Lotufo Neto, Francisco; Hirata, Mario Hiroyuki ; Brisighelli, Francesca; Páramo, Mario; Carracedo, Ángel M; Brion, Maria
Fonte: Forensic Science International. Unidades: FM, FCF
Assuntos: FARMACOCINÉTICA, FARMACODINÂMICA
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ABNT
MATILLA, Marina Martinez et al. Genetic susceptibility in pharmacodynamic and pharmacokinetic pathways underlying drug-induced arrhythmia and sudden unexplained deaths. Forensic Science International, v. 42, p. 203-212, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.fsigen.2019.07.010. Acesso em: 02 jul. 2024.
APA
Matilla, M. M., Verea, A. J. B., Santori, M., Bermejo, J. A., Luis, E. R., Gil, R., et al. (2019). Genetic susceptibility in pharmacodynamic and pharmacokinetic pathways underlying drug-induced arrhythmia and sudden unexplained deaths. Forensic Science International, 42, 203-212. doi:10.1016/j.fsigen.2019.07.010
NLM
Matilla MM, Verea AJB, Santori M, Bermejo JA, Luis ER, Gil R, Bermejo AM, Lotufo Neto F, Hirata MH, Brisighelli F, Páramo M, Carracedo ÁM, Brion M. Genetic susceptibility in pharmacodynamic and pharmacokinetic pathways underlying drug-induced arrhythmia and sudden unexplained deaths [Internet]. Forensic Science International. 2019 ; 42 203-212.[citado 2024 jul. 02 ] Available from: https://doi.org/10.1016/j.fsigen.2019.07.010
Vancouver
Matilla MM, Verea AJB, Santori M, Bermejo JA, Luis ER, Gil R, Bermejo AM, Lotufo Neto F, Hirata MH, Brisighelli F, Páramo M, Carracedo ÁM, Brion M. Genetic susceptibility in pharmacodynamic and pharmacokinetic pathways underlying drug-induced arrhythmia and sudden unexplained deaths [Internet]. Forensic Science International. 2019 ; 42 203-212.[citado 2024 jul. 02 ] Available from: https://doi.org/10.1016/j.fsigen.2019.07.010
Trabalho de evento-resumo periodico
Next generation sequencing in the diagnosis of familial hypercholesterolemia (2017)
Borges, Jessica Bassabi; Bastos, Gisele Medeiros; Afonso, Thais Kristini Almendros; Rodrigues, Elisângela da Silva; Thurow, Helena Strelow; Faludi, André Arpad; Gonçalves, Rodrigo Marques; Sousa, Amanda Guerra de Moraes Rego; Hirata, Rosario Dominguez Crespo ; Hirata, Mario Hiroyuki
Fonte: Atherosclerosis. Nome do evento: European Atherosclerosis Society Congress (EAS). Unidade: FCF
Assuntos: HIPERCOLESTEROLEMIA, VARIAÇÃO GENÉTICA, RATOS
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ABNT
BORGES, Jessica Bassabi et al. Next generation sequencing in the diagnosis of familial hypercholesterolemia. Atherosclerosis. Clare: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 02 jul. 2024. , 2017
APA
Borges, J. B., Bastos, G. M., Afonso, T. K. A., Rodrigues, E. da S., Thurow, H. S., Faludi, A. A., et al. (2017). Next generation sequencing in the diagnosis of familial hypercholesterolemia. Atherosclerosis. Clare: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.
NLM
Borges JB, Bastos GM, Afonso TKA, Rodrigues E da S, Thurow HS, Faludi AA, Gonçalves RM, Sousa AG de MR, Hirata RDC, Hirata MH. Next generation sequencing in the diagnosis of familial hypercholesterolemia. Atherosclerosis. 2017 ; 263 e282 res. PO558.[citado 2024 jul. 02 ]
Vancouver
Borges JB, Bastos GM, Afonso TKA, Rodrigues E da S, Thurow HS, Faludi AA, Gonçalves RM, Sousa AG de MR, Hirata RDC, Hirata MH. Next generation sequencing in the diagnosis of familial hypercholesterolemia. Atherosclerosis. 2017 ; 263 e282 res. PO558.[citado 2024 jul. 02 ]
Trabalho de evento-resumo periodico
Study of APOB mutations and familial hypercholesterolemia phenotypes (2016)
Borges, J. Bassani; Bastos, G. Medeiros; Afonso, T. K. Almendros; Rodrigues, E. da Silva; Thurow, Helena Strelow; Hirata, Thiago Dominguez Crespo; Faludi, André Arpad; Gonçalves, R. Mendes; Hirata, Rosario Dominguez Crespo ; Hirata, Mario Hiroyuki
Fonte: Atherosclerosis. Nome do evento: European Atherosclerosis Society Congress. Unidade: FCF
Assuntos: DISLIPIDEMIAS, HIPERCOLESTEROLEMIA
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ABNT
BORGES, J. Bassani et al. Study of APOB mutations and familial hypercholesterolemia phenotypes. Atherosclerosis. Clare: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 02 jul. 2024. , 2016
APA
Borges, J. B., Bastos, G. M., Afonso, T. K. A., Rodrigues, E. da S., Thurow, H. S., Hirata, T. D. C., et al. (2016). Study of APOB mutations and familial hypercholesterolemia phenotypes. Atherosclerosis. Clare: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.
NLM
Borges JB, Bastos GM, Afonso TKA, Rodrigues E da S, Thurow HS, Hirata TDC, Faludi AA, Gonçalves RM, Hirata RDC, Hirata MH. Study of APOB mutations and familial hypercholesterolemia phenotypes. Atherosclerosis. 2016 ; 252 e43 res. EAS16-0766.[citado 2024 jul. 02 ]
Vancouver
Borges JB, Bastos GM, Afonso TKA, Rodrigues E da S, Thurow HS, Hirata TDC, Faludi AA, Gonçalves RM, Hirata RDC, Hirata MH. Study of APOB mutations and familial hypercholesterolemia phenotypes. Atherosclerosis. 2016 ; 252 e43 res. EAS16-0766.[citado 2024 jul. 02 ]
Trabalho de evento-resumo periodico
Acute coronary syndrome and gene polymorphisms influence leukocyte MRNA expression of adhesion molecules and inflammatory proteins (2014)
Hirata, Mario Hiroyuki ; Cavichioli, Débora; Germano, Juliana de Freitas; Braga, Aécio Assunção; Cerda, Alvaro; Fajardo, Cristina Moreno ; Sampaio, M. F; Santos, E. B; Menuso, L; Sousa, A. G. M. R; Hirata, Rosario Dominguez Crespo
Fonte: Atherosclerosis. Nome do evento: European Atherosclerosis Society Congress (EAS). Unidade: FCF
Assuntos: POLIMORFISMO, DOENÇAS CARDIOVASCULARES
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ABNT
HIRATA, Mario Hiroyuki et al. Acute coronary syndrome and gene polymorphisms influence leukocyte MRNA expression of adhesion molecules and inflammatory proteins. Atherosclerosis. Clare: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 02 jul. 2024. , 2014
APA
Hirata, M. H., Cavichioli, D., Germano, J. de F., Braga, A. A., Cerda, A., Fajardo, C. M., et al. (2014). Acute coronary syndrome and gene polymorphisms influence leukocyte MRNA expression of adhesion molecules and inflammatory proteins. Atherosclerosis. Clare: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.
NLM
Hirata MH, Cavichioli D, Germano J de F, Braga AA, Cerda A, Fajardo CM, Sampaio MF, Santos EB, Menuso L, Sousa AGMR, Hirata RDC. Acute coronary syndrome and gene polymorphisms influence leukocyte MRNA expression of adhesion molecules and inflammatory proteins. Atherosclerosis. 2014 ; 235( 2): e41 res. EAS-0819.[citado 2024 jul. 02 ]
Vancouver
Hirata MH, Cavichioli D, Germano J de F, Braga AA, Cerda A, Fajardo CM, Sampaio MF, Santos EB, Menuso L, Sousa AGMR, Hirata RDC. Acute coronary syndrome and gene polymorphisms influence leukocyte MRNA expression of adhesion molecules and inflammatory proteins. Atherosclerosis. 2014 ; 235( 2): e41 res. EAS-0819.[citado 2024 jul. 02 ]
Trabalho de evento-resumo periodico
Dowregulation of monocyte adhesion molecules by inhibition of synthesis and absorption of cholesterol (2014)
Cerda, Alvaro; Rodrigues, Alice Cristina ; Alves, Camila; Genvigir, Fabiana Dalla Vecchia; Fajardo, Cristina Moreno ; Dórea, Egidio Lima; Gusukuma, Maria Cecília; Pinto, Gelson de Almeida; Hirata, Mario Hiroyuki ; Hirata, Rosario Dominguez Crespo
Fonte: Atherosclerosis. Nome do evento: European Atherosclerosis Society Congress (EAS). Unidades: ICB, FCF, HU
Assuntos: COLESTEROL, MONÓCITOS
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ABNT
CERDA, Alvaro et al. Dowregulation of monocyte adhesion molecules by inhibition of synthesis and absorption of cholesterol. Atherosclerosis. Clare: Instituto de Ciências Biomédicas, Universidade de São Paulo. . Acesso em: 02 jul. 2024. , 2014
APA
Cerda, A., Rodrigues, A. C., Alves, C., Genvigir, F. D. V., Fajardo, C. M., Dórea, E. L., et al. (2014). Dowregulation of monocyte adhesion molecules by inhibition of synthesis and absorption of cholesterol. Atherosclerosis. Clare: Instituto de Ciências Biomédicas, Universidade de São Paulo.
NLM
Cerda A, Rodrigues AC, Alves C, Genvigir FDV, Fajardo CM, Dórea EL, Gusukuma MC, Pinto G de A, Hirata MH, Hirata RDC. Dowregulation of monocyte adhesion molecules by inhibition of synthesis and absorption of cholesterol. Atherosclerosis. 2014 ; 235( 2): e255 res. EAS-0490.[citado 2024 jul. 02 ]
Vancouver
Cerda A, Rodrigues AC, Alves C, Genvigir FDV, Fajardo CM, Dórea EL, Gusukuma MC, Pinto G de A, Hirata MH, Hirata RDC. Dowregulation of monocyte adhesion molecules by inhibition of synthesis and absorption of cholesterol. Atherosclerosis. 2014 ; 235( 2): e255 res. EAS-0490.[citado 2024 jul. 02 ]
Artigo de periodico
Low bone mineral density is associated to poor glycemic control and increased OPG expression in children and adolescents with type 1 diabetes (2014)
Loureiro, Melina Bezerra; Ururahy, Marcela Abbott Galvão; Neto, Francisco P. Freire; Oliveira, Gustavo H.M; Duarte, Valeria M.G; Luchessi, André Ducati; Neto, Jose´ Brandão; Hirata, Rosario Dominguez Crespo ; Hirata, Mario Hiroyuki ; Maciel Neto, Jose´ J; Arrais, Ricardo Fernando; Almeida, Maria G; Rezende, Adriana A
Fonte: Diabetes Research and Clinical Practice. Unidade: FCF
Assuntos: DIABETES MELLITUS INSULINO-DEPENDENTE, GLICEMIA
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ABNT
LOUREIRO, Melina Bezerra et al. Low bone mineral density is associated to poor glycemic control and increased OPG expression in children and adolescents with type 1 diabetes. Diabetes Research and Clinical Practice, v. 103, n. 3, p. 452-457, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.diabres.2013.12.018. Acesso em: 02 jul. 2024.
APA
Loureiro, M. B., Ururahy, M. A. G., Neto, F. P. F., Oliveira, G. H. M., Duarte, V. M. G., Luchessi, A. D., et al. (2014). Low bone mineral density is associated to poor glycemic control and increased OPG expression in children and adolescents with type 1 diabetes. Diabetes Research and Clinical Practice, 103( 3), 452-457. doi:10.1016/j.diabres.2013.12.018
NLM
Loureiro MB, Ururahy MAG, Neto FPF, Oliveira GHM, Duarte VMG, Luchessi AD, Neto J´ B, Hirata RDC, Hirata MH, Maciel Neto J´ J, Arrais RF, Almeida MG, Rezende AA. Low bone mineral density is associated to poor glycemic control and increased OPG expression in children and adolescents with type 1 diabetes [Internet]. Diabetes Research and Clinical Practice. 2014 ; 103( 3): 452-457.[citado 2024 jul. 02 ] Available from: https://doi.org/10.1016/j.diabres.2013.12.018
Vancouver
Loureiro MB, Ururahy MAG, Neto FPF, Oliveira GHM, Duarte VMG, Luchessi AD, Neto J´ B, Hirata RDC, Hirata MH, Maciel Neto J´ J, Arrais RF, Almeida MG, Rezende AA. Low bone mineral density is associated to poor glycemic control and increased OPG expression in children and adolescents with type 1 diabetes [Internet]. Diabetes Research and Clinical Practice. 2014 ; 103( 3): 452-457.[citado 2024 jul. 02 ] Available from: https://doi.org/10.1016/j.diabres.2013.12.018
Artigo de periodico
Genetic population data of 12 STR loci of the PowerPlex(R) Y system in the state of Sao Paulo population (Southeast of Brazil) (2008)
Góis, Carolina Costa; Martins, Joyce Aparecida; Pereira, Gabriella Augusto; Freschi, Adriana; Paneto, Greiciane Gaburro; Alvarenga, Vera Lucy de Santi; Cicarelli, Regina Maria Barretto; Hirata, Mario Hiroyuki ; Oliveira, Rogério Nogueira de
Fonte: Forensic Science International. Unidades: FCF, FO
Assuntos: GENÉTICA DE POPULAÇÕES, CROMOSSOMO Y
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ABNT
GÓIS, Carolina Costa et al. Genetic population data of 12 STR loci of the PowerPlex(R) Y system in the state of Sao Paulo population (Southeast of Brazil). Forensic Science International, v. 174, n. 1, p. 80-85, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.forsciint.2006.12.018. Acesso em: 02 jul. 2024.
APA
Góis, C. C., Martins, J. A., Pereira, G. A., Freschi, A., Paneto, G. G., Alvarenga, V. L. de S., et al. (2008). Genetic population data of 12 STR loci of the PowerPlex(R) Y system in the state of Sao Paulo population (Southeast of Brazil). Forensic Science International, 174( 1), 80-85. doi:10.1016/j.forsciint.2006.12.018
NLM
Góis CC, Martins JA, Pereira GA, Freschi A, Paneto GG, Alvarenga VL de S, Cicarelli RMB, Hirata MH, Oliveira RN de. Genetic population data of 12 STR loci of the PowerPlex(R) Y system in the state of Sao Paulo population (Southeast of Brazil) [Internet]. Forensic Science International. 2008 ;174( 1): 80-85.[citado 2024 jul. 02 ] Available from: https://doi.org/10.1016/j.forsciint.2006.12.018
Vancouver
Góis CC, Martins JA, Pereira GA, Freschi A, Paneto GG, Alvarenga VL de S, Cicarelli RMB, Hirata MH, Oliveira RN de. Genetic population data of 12 STR loci of the PowerPlex(R) Y system in the state of Sao Paulo population (Southeast of Brazil) [Internet]. Forensic Science International. 2008 ;174( 1): 80-85.[citado 2024 jul. 02 ] Available from: https://doi.org/10.1016/j.forsciint.2006.12.018
Artigo de periodico
Heteroplasmy in hair: differences among hair and blood from the same individuals are still a matter of debate (2007)
Paneto, Greiciane Gaburro; Martins, Joyce Aparecida; Longo, Larissa Valle Guilhen; Pereira, Gabriella Augusto; Freschi, Adriana; Alvarenga, Vera Lucy de Santi; Chen, Bety; Oliveira, Rogério Nogueira de; Hirata, Mario Hiroyuki ; Cicarelli, Regina Maria Barretto
Fonte: Forensic Science International. Unidades: FO, FCF
Assuntos: DNA MITOCONDRIAL, GENÉTICA
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ABNT
PANETO, Greiciane Gaburro et al. Heteroplasmy in hair: differences among hair and blood from the same individuals are still a matter of debate. Forensic Science International, v. 173, n. 2-3, p. 117-121, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.forsciint.2007.02.011. Acesso em: 02 jul. 2024.
APA
Paneto, G. G., Martins, J. A., Longo, L. V. G., Pereira, G. A., Freschi, A., Alvarenga, V. L. de S., et al. (2007). Heteroplasmy in hair: differences among hair and blood from the same individuals are still a matter of debate. Forensic Science International, 173( 2-3), 117-121. doi:10.1016/j.forsciint.2007.02.011
NLM
Paneto GG, Martins JA, Longo LVG, Pereira GA, Freschi A, Alvarenga VL de S, Chen B, Oliveira RN de, Hirata MH, Cicarelli RMB. Heteroplasmy in hair: differences among hair and blood from the same individuals are still a matter of debate [Internet]. Forensic Science International. 2007 ; 173( 2-3): 117-121.[citado 2024 jul. 02 ] Available from: https://doi.org/10.1016/j.forsciint.2007.02.011
Vancouver
Paneto GG, Martins JA, Longo LVG, Pereira GA, Freschi A, Alvarenga VL de S, Chen B, Oliveira RN de, Hirata MH, Cicarelli RMB. Heteroplasmy in hair: differences among hair and blood from the same individuals are still a matter of debate [Internet]. Forensic Science International. 2007 ; 173( 2-3): 117-121.[citado 2024 jul. 02 ] Available from: https://doi.org/10.1016/j.forsciint.2007.02.011
Trabalho de evento-resumo periodico
Molecular basis of familial hypercholesterolemia in Brazil: Identification of nine novel LDLR gene mutations (2002)
Salazar, Luís Antônio; Hirata, Mario Hiroyuki ; Cavalli, Selma Andrea; Nakandakare, Edna Regina; Forti, Neusa Assumpta; Diament, Jayme; Giannini, S.; Bertolami, Marcelo Chiara; Hirata, Rosario Dominguez Crespo
Fonte: Atherosclerosis. Nome do evento: Congress of the European Atherosclerosis Society. Unidades: FCF, FM
Assuntos: HIPERCOLESTEROLEMIA, MUTAÇÃO GENÉTICA, BIOQUÍMICA
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ABNT
SALAZAR, Luís Antônio et al. Molecular basis of familial hypercholesterolemia in Brazil: Identification of nine novel LDLR gene mutations. Atherosclerosis. Clare: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 02 jul. 2024. , 2002
APA
Salazar, L. A., Hirata, M. H., Cavalli, S. A., Nakandakare, E. R., Forti, N. A., Diament, J., et al. (2002). Molecular basis of familial hypercholesterolemia in Brazil: Identification of nine novel LDLR gene mutations. Atherosclerosis. Clare: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.
NLM
Salazar LA, Hirata MH, Cavalli SA, Nakandakare ER, Forti NA, Diament J, Giannini S, Bertolami MC, Hirata RDC. Molecular basis of familial hypercholesterolemia in Brazil: Identification of nine novel LDLR gene mutations. Atherosclerosis. 2002 ; 3/2 200 res. 621.[citado 2024 jul. 02 ]
Vancouver
Salazar LA, Hirata MH, Cavalli SA, Nakandakare ER, Forti NA, Diament J, Giannini S, Bertolami MC, Hirata RDC. Molecular basis of familial hypercholesterolemia in Brazil: Identification of nine novel LDLR gene mutations. Atherosclerosis. 2002 ; 3/2 200 res. 621.[citado 2024 jul. 02 ]
Trabalho de evento-resumo periodico
Influence of LDL receptor gene polymorphisms on serum lipid levels and response to atorvastatin in subjects with familial and non familial hypercholesterolemia (2002)
Salazar, Luís Antônio; Hirata, Mario Hiroyuki ; Cavalli, Selma Andrea; Nakandakare, Edna Regina; Forti, Neusa Assumpta; Diament, Jayme; Giannini, S. D.; Bertolami, Marcelo Chiara; Hirata, Rosario Dominguez Crespo
Fonte: Atherosclerosis. Nome do evento: Congress of the European Atherosclerosis Society. Unidades: FCF, FM
Assuntos: BIOQUÍMICA, HIPERCOLESTEROLEMIA (AVALIAÇÃO), LIPÍDEOS, MEDICAMENTO (AVALIAÇÃO;CONTROLE), GENÉTICA
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ABNT
SALAZAR, Luís Antônio et al. Influence of LDL receptor gene polymorphisms on serum lipid levels and response to atorvastatin in subjects with familial and non familial hypercholesterolemia. Atherosclerosis. Clare: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 02 jul. 2024. , 2002
APA
Salazar, L. A., Hirata, M. H., Cavalli, S. A., Nakandakare, E. R., Forti, N. A., Diament, J., et al. (2002). Influence of LDL receptor gene polymorphisms on serum lipid levels and response to atorvastatin in subjects with familial and non familial hypercholesterolemia. Atherosclerosis. Clare: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.
NLM
Salazar LA, Hirata MH, Cavalli SA, Nakandakare ER, Forti NA, Diament J, Giannini SD, Bertolami MC, Hirata RDC. Influence of LDL receptor gene polymorphisms on serum lipid levels and response to atorvastatin in subjects with familial and non familial hypercholesterolemia. Atherosclerosis. 2002 ; 3/2 125 res. 273.[citado 2024 jul. 02 ]
Vancouver
Salazar LA, Hirata MH, Cavalli SA, Nakandakare ER, Forti NA, Diament J, Giannini SD, Bertolami MC, Hirata RDC. Influence of LDL receptor gene polymorphisms on serum lipid levels and response to atorvastatin in subjects with familial and non familial hypercholesterolemia. Atherosclerosis. 2002 ; 3/2 125 res. 273.[citado 2024 jul. 02 ]
Trabalho de evento-resumo periodico
Alpha-thalassemia diagnosis by PCR in individuals with microcytosis and hypochromia (2000)
Strufaldi, C.; Yokomizo, Iara Keiko; Hirata, Rosario Dominguez Crespo ; Hirata, Mario Hiroyuki ; Silveira, P A; Gualandro, Sandra Fátima Menosi
Fonte: International Journal of Hematology. Nome do evento: World Congress of the International Society of Hematology. Unidades: FM, FCF
Assuntos: TÉCNICAS E PROCEDIMENTOS DE LABORATÓRIO, HEMATOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
STRUFALDI, C. et al. Alpha-thalassemia diagnosis by PCR in individuals with microcytosis and hypochromia. International Journal of Hematology. Limerick: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 02 jul. 2024. , 2000
APA
Strufaldi, C., Yokomizo, I. K., Hirata, R. D. C., Hirata, M. H., Silveira, P. A., & Gualandro, S. F. M. (2000). Alpha-thalassemia diagnosis by PCR in individuals with microcytosis and hypochromia. International Journal of Hematology. Limerick: Faculdade de Medicina, Universidade de São Paulo.
NLM
Strufaldi C, Yokomizo IK, Hirata RDC, Hirata MH, Silveira PA, Gualandro SFM. Alpha-thalassemia diagnosis by PCR in individuals with microcytosis and hypochromia. International Journal of Hematology. 2000 ; 72 209.[citado 2024 jul. 02 ]
Vancouver
Strufaldi C, Yokomizo IK, Hirata RDC, Hirata MH, Silveira PA, Gualandro SFM. Alpha-thalassemia diagnosis by PCR in individuals with microcytosis and hypochromia. International Journal of Hematology. 2000 ; 72 209.[citado 2024 jul. 02 ]

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