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Trabalho de evento-resumo periodico
Short form health survey (SF-36) differs between genotypic groups of patients with suspected hereditary hemochromatosis (2017)
Fernanda, Paula; Gualandro, Sandra Fátima Menosi; Krieger, Jose
Source: American journal of hematology. Conference titles: Congress of the international Biolron society - IBIS. Unidade: FM
Subjects: DOENÇAS GENÉTICAS, HEMOCROMATOSE
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ABNT
FERNANDA, Paula e GUALANDRO, Sandra Fátima Menosi e KRIEGER, Jose. Short form health survey (SF-36) differs between genotypic groups of patients with suspected hereditary hemochromatosis. American journal of hematology. Hoboken: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 14 nov. 2024. , 2017
APA
Fernanda, P., Gualandro, S. F. M., & Krieger, J. (2017). Short form health survey (SF-36) differs between genotypic groups of patients with suspected hereditary hemochromatosis. American journal of hematology. Hoboken: Faculdade de Medicina, Universidade de São Paulo.
NLM
Fernanda P, Gualandro SFM, Krieger J. Short form health survey (SF-36) differs between genotypic groups of patients with suspected hereditary hemochromatosis. American journal of hematology. 2017 ; 92( 8): E469-E469.[citado 2024 nov. 14 ]
Vancouver
Fernanda P, Gualandro SFM, Krieger J. Short form health survey (SF-36) differs between genotypic groups of patients with suspected hereditary hemochromatosis. American journal of hematology. 2017 ; 92( 8): E469-E469.[citado 2024 nov. 14 ]
Artigo de periodico
A prospective study of patients with refractory angina: outcomes and the role of high-sensitivity troponin T (2017)
Poppi, Nilson T.; Gowdak, Luís H. W.; Dourado, Luciana O. C.; Adam, Eduardo L.; Leite, Thiago N. P.; Mioto, Bruno M.; Krieger, José E.; César, Luiz A. M.; Pereira, Alexandre C.
Source: Clinical Cardiology. Unidade: FM
Subjects: ANGINA INSTÁVEL, PROGNÓSTICO, ESTUDOS PROSPECTIVOS, REVASCULARIZAÇÃO MIOCÁRDICA
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ABNT
POPPI, Nilson T. et al. A prospective study of patients with refractory angina: outcomes and the role of high-sensitivity troponin T. Clinical Cardiology, v. 40, n. 1, p. 11-17, 2017Tradução . . Disponível em: http://onlinelibrary.wiley.com/doi/10.1002/clc.22599/epdf. Acesso em: 14 nov. 2024.
APA
Poppi, N. T., Gowdak, L. H. W., Dourado, L. O. C., Adam, E. L., Leite, T. N. P., Mioto, B. M., et al. (2017). A prospective study of patients with refractory angina: outcomes and the role of high-sensitivity troponin T. Clinical Cardiology, 40( 1), 11-17. doi:10.1002/clc.22599
NLM
Poppi NT, Gowdak LHW, Dourado LOC, Adam EL, Leite TNP, Mioto BM, Krieger JE, César LAM, Pereira AC. A prospective study of patients with refractory angina: outcomes and the role of high-sensitivity troponin T [Internet]. Clinical Cardiology. 2017 ; 40( 1): 11-17.[citado 2024 nov. 14 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/clc.22599/epdf
Vancouver
Poppi NT, Gowdak LHW, Dourado LOC, Adam EL, Leite TNP, Mioto BM, Krieger JE, César LAM, Pereira AC. A prospective study of patients with refractory angina: outcomes and the role of high-sensitivity troponin T [Internet]. Clinical Cardiology. 2017 ; 40( 1): 11-17.[citado 2024 nov. 14 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/clc.22599/epdf
Artigo de periodico
Evaluation of clinical and laboratory parameters used in the identification of index cases for genetic screening of familial hypercholesterolemia in Brazil (2017)
Silva, Pãmela R. S; Silva, Pãmela R. S; Jannes, Cinthia E; Oliveira, Theo G. M; Miname, Marcio H; Rocha, Viviane Z; Chacra, Ana Paula; Gurgel, Maria Helane C; Montenegro, Renan M; Rodrigues Sobrinho, Carlos Roberto M; Moreira, Annie Seixas Bello; Assad, Marcelo H. V; Pinto, Marina R. C; Tada, Mauricio Teruo; Santos Filho, Raul Dias dos; Pereira, Alexandre C; Krieger, José Eduardo
Source: Atherosclerosis. Unidade: FM
Subjects: HIPERCOLESTEROLEMIA, CALCIFICAÇÃO FISIOLÓGICA
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ABNT
SILVA, Pãmela R. S et al. Evaluation of clinical and laboratory parameters used in the identification of index cases for genetic screening of familial hypercholesterolemia in Brazil. Atherosclerosis, v. 263, p. 257-262, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.atherosclerosis.2017.06.917. Acesso em: 14 nov. 2024.
APA
Silva, P. R. S., Silva, P. R. S., Jannes, C. E., Oliveira, T. G. M., Miname, M. H., Rocha, V. Z., et al. (2017). Evaluation of clinical and laboratory parameters used in the identification of index cases for genetic screening of familial hypercholesterolemia in Brazil. Atherosclerosis, 263, 257-262. doi:10.1016/j.atherosclerosis.2017.06.917
NLM
Silva PRS, Silva PRS, Jannes CE, Oliveira TGM, Miname MH, Rocha VZ, Chacra AP, Gurgel MHC, Montenegro RM, Rodrigues Sobrinho CRM, Moreira ASB, Assad MHV, Pinto MRC, Tada MT, Santos Filho RD dos, Pereira AC, Krieger JE. Evaluation of clinical and laboratory parameters used in the identification of index cases for genetic screening of familial hypercholesterolemia in Brazil [Internet]. Atherosclerosis. 2017 ; 263 257-262.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.atherosclerosis.2017.06.917
Vancouver
Silva PRS, Silva PRS, Jannes CE, Oliveira TGM, Miname MH, Rocha VZ, Chacra AP, Gurgel MHC, Montenegro RM, Rodrigues Sobrinho CRM, Moreira ASB, Assad MHV, Pinto MRC, Tada MT, Santos Filho RD dos, Pereira AC, Krieger JE. Evaluation of clinical and laboratory parameters used in the identification of index cases for genetic screening of familial hypercholesterolemia in Brazil [Internet]. Atherosclerosis. 2017 ; 263 257-262.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.atherosclerosis.2017.06.917
Trabalho de evento-resumo periodico
High heritability of telomere lingth in families with bipolar disorder (2017)
Martinez, Daniela; Millischer, Vincent; Michelon, Leandro; Camilo, Caroline; Brentani, Helena Paula; Esteban, Nubia; Krieger, José Eduardo; Pereira, Alexandre; Lavebratt, Catharina; Schalling, Martin; Vallada Filho, Homero Pinto
Source: European neuropsychopharmacology. Conference titles: Annual World Congress of Psychiatric Genetics (WCPG). Unidade: FM
Subjects: TRANSTORNO BIPOLAR, TELÔMERO, PSIQUIATRIA, FAMÍLIA
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ABNT
MARTINEZ, Daniela et al. High heritability of telomere lingth in families with bipolar disorder. European neuropsychopharmacology. Amsterdam: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 14 nov. 2024. , 2017
APA
Martinez, D., Millischer, V., Michelon, L., Camilo, C., Brentani, H. P., Esteban, N., et al. (2017). High heritability of telomere lingth in families with bipolar disorder. European neuropsychopharmacology. Amsterdam: Faculdade de Medicina, Universidade de São Paulo.
NLM
Martinez D, Millischer V, Michelon L, Camilo C, Brentani HP, Esteban N, Krieger JE, Pereira A, Lavebratt C, Schalling M, Vallada Filho HP. High heritability of telomere lingth in families with bipolar disorder. European neuropsychopharmacology. 2017 ; 27 S387.[citado 2024 nov. 14 ]
Vancouver
Martinez D, Millischer V, Michelon L, Camilo C, Brentani HP, Esteban N, Krieger JE, Pereira A, Lavebratt C, Schalling M, Vallada Filho HP. High heritability of telomere lingth in families with bipolar disorder. European neuropsychopharmacology. 2017 ; 27 S387.[citado 2024 nov. 14 ]
Artigo de periodico
A Novel Aldosterone Antagonist Limits Renal Injury in 5/6 Nephrectomy (2017)
Fujihara, Clarice K.; Kowala, M. C.; Breyer, M. D.; Sena, Claudia R.; Rodrigues, Mariliza V.; Arias, Simone C. A.; Fanelli, Camilla; Malheiros, Denise M.; Jadhav, P. K.; Montrose-Rafizadeh, Chahrzad; Krieger, Jose E.; Zatz, Roberto
Source: Scientific Reports. Unidade: FM
Subjects: RATOS WISTAR, INSUFICIÊNCIA RENAL CRÔNICA, FÁRMACOS DO SANGUE E SISTEMA HEMATOPOÉTICO
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ABNT
FUJIHARA, Clarice K. et al. A Novel Aldosterone Antagonist Limits Renal Injury in 5/6 Nephrectomy. Scientific Reports, v. 7, n. 7733, p. 1-12, 2017Tradução . . Disponível em: https://doi.org/10.1038/s41598-017-08383-2. Acesso em: 14 nov. 2024.
APA
Fujihara, C. K., Kowala, M. C., Breyer, M. D., Sena, C. R., Rodrigues, M. V., Arias, S. C. A., et al. (2017). A Novel Aldosterone Antagonist Limits Renal Injury in 5/6 Nephrectomy. Scientific Reports, 7( 7733), 1-12. doi:10.1038/s41598-017-08383-2
NLM
Fujihara CK, Kowala MC, Breyer MD, Sena CR, Rodrigues MV, Arias SCA, Fanelli C, Malheiros DM, Jadhav PK, Montrose-Rafizadeh C, Krieger JE, Zatz R. A Novel Aldosterone Antagonist Limits Renal Injury in 5/6 Nephrectomy [Internet]. Scientific Reports. 2017 ; 7( 7733): 1-12.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1038/s41598-017-08383-2
Vancouver
Fujihara CK, Kowala MC, Breyer MD, Sena CR, Rodrigues MV, Arias SCA, Fanelli C, Malheiros DM, Jadhav PK, Montrose-Rafizadeh C, Krieger JE, Zatz R. A Novel Aldosterone Antagonist Limits Renal Injury in 5/6 Nephrectomy [Internet]. Scientific Reports. 2017 ; 7( 7733): 1-12.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1038/s41598-017-08383-2
Artigo de periodico
Clinical and molecular aspects of familial hypercholesterolemia in Ibero-American countries (2017)
Santos, Raul D.; Bourbon, Mafalda; Alonso, Rodrigo; Cuevas, Ada; Vasques-Cardenas, Norma Alexandra; Pereira, Alexandre C.; Merchan, Alonso; Alves, Ana Catarina; Medeiros, Ana Margarida; Jannes, Cinthia E.; Krieger, Jose E.; Schreier, Laura; Isla, Leopoldo Perez de; Magana-Torres, Maria Teresa; Stoll, Mario; Mata, Nelva; Dell Oca, Nicolas; Corral, Pablo; Asenjo, Sylvia; Banares, Virginia G.; Reyes, Ximena; Mata, Pedro
Source: Journal of clinical lipidology. Unidade: FM
Subjects: RASTREAMENTO, COLESTEROL, HIPERCOLESTEROLEMIA, ARTERIOSCLEROSE
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ABNT
SANTOS, Raul D. et al. Clinical and molecular aspects of familial hypercholesterolemia in Ibero-American countries. Journal of clinical lipidology, n. 1, p. 160-166, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.jacl.2016.11.004. Acesso em: 14 nov. 2024.
APA
Santos, R. D., Bourbon, M., Alonso, R., Cuevas, A., Vasques-Cardenas, N. A., Pereira, A. C., et al. (2017). Clinical and molecular aspects of familial hypercholesterolemia in Ibero-American countries. Journal of clinical lipidology, ( 1), 160-166. doi:10.1016/j.jacl.2016.11.004
NLM
Santos RD, Bourbon M, Alonso R, Cuevas A, Vasques-Cardenas NA, Pereira AC, Merchan A, Alves AC, Medeiros AM, Jannes CE, Krieger JE, Schreier L, Isla LP de, Magana-Torres MT, Stoll M, Mata N, Dell Oca N, Corral P, Asenjo S, Banares VG, Reyes X, Mata P. Clinical and molecular aspects of familial hypercholesterolemia in Ibero-American countries [Internet]. Journal of clinical lipidology. 2017 ;( 1): 160-166.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.jacl.2016.11.004
Vancouver
Santos RD, Bourbon M, Alonso R, Cuevas A, Vasques-Cardenas NA, Pereira AC, Merchan A, Alves AC, Medeiros AM, Jannes CE, Krieger JE, Schreier L, Isla LP de, Magana-Torres MT, Stoll M, Mata N, Dell Oca N, Corral P, Asenjo S, Banares VG, Reyes X, Mata P. Clinical and molecular aspects of familial hypercholesterolemia in Ibero-American countries [Internet]. Journal of clinical lipidology. 2017 ;( 1): 160-166.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.jacl.2016.11.004
Trabalho de evento-resumo
Biased agonism in AT1R by molecular dynamics (2017)
Modestia, Silvestre Massimo; A., Eric; Krieger, José Eduardo; Rangel-Yagui, Carlota de Oliveira
Source: Abstracts. Conference titles: Brazilian Biophysical Society Congress. Unidades: FM, FCF
Subjects: PEPTÍDEOS, ANGIOTENSINA II
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ABNT
MODESTIA, Silvestre Massimo et al. Biased agonism in AT1R by molecular dynamics. 2017, Anais.. Rio de Janeiro: Sociedade Brasileira de Biofísica/SBBF, 2017. Disponível em: http://www.sbbf.org.br/xliisbbf2017/wp-content/uploads/2017/05/Scientific-Program-SBBf2017.pdf. Acesso em: 14 nov. 2024.
APA
Modestia, S. M., A., E., Krieger, J. E., & Rangel-Yagui, C. de O. (2017). Biased agonism in AT1R by molecular dynamics. In Abstracts. Rio de Janeiro: Sociedade Brasileira de Biofísica/SBBF. Recuperado de http://www.sbbf.org.br/xliisbbf2017/wp-content/uploads/2017/05/Scientific-Program-SBBf2017.pdf
NLM
Modestia SM, A. E, Krieger JE, Rangel-Yagui C de O. Biased agonism in AT1R by molecular dynamics [Internet]. Abstracts. 2017 ;[citado 2024 nov. 14 ] Available from: http://www.sbbf.org.br/xliisbbf2017/wp-content/uploads/2017/05/Scientific-Program-SBBf2017.pdf
Vancouver
Modestia SM, A. E, Krieger JE, Rangel-Yagui C de O. Biased agonism in AT1R by molecular dynamics [Internet]. Abstracts. 2017 ;[citado 2024 nov. 14 ] Available from: http://www.sbbf.org.br/xliisbbf2017/wp-content/uploads/2017/05/Scientific-Program-SBBf2017.pdf
Trabalho de evento-resumo periodico
Heritability and shared genetic factors for symptoms of anxiety and depression in a brazilian family-based cohort, the baependI study (2017)
Taporoski, Tâmara; Negrão, Andre Brooking; Horimoto, André R. V. R; Duarte, Núbia E; Alvim, Rafael O.; Oliveira, Camila M. de; Krieger, José Eduardo; Von chantz, Malcolm; Vallada Filho, Homero Pinto; Pereira, Alexandre C
Source: European neuropsychopharmacology. Conference titles: Annual World Congress of Psychiatric Genetics (WCPG). Unidade: FM
Subjects: DEPRESSÃO, ANSIEDADE, GENÉTICA, HEREDITARIEDADE
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ABNT
TAPOROSKI, Tâmara et al. Heritability and shared genetic factors for symptoms of anxiety and depression in a brazilian family-based cohort, the baependI study. European neuropsychopharmacology. Amsterdam: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 14 nov. 2024. , 2017
APA
Taporoski, T., Negrão, A. B., Horimoto, A. R. V. R., Duarte, N. E., Alvim, R. O., Oliveira, C. M. de, et al. (2017). Heritability and shared genetic factors for symptoms of anxiety and depression in a brazilian family-based cohort, the baependI study. European neuropsychopharmacology. Amsterdam: Faculdade de Medicina, Universidade de São Paulo.
NLM
Taporoski T, Negrão AB, Horimoto ARVR, Duarte NE, Alvim RO, Oliveira CM de, Krieger JE, Von chantz M, Vallada Filho HP, Pereira AC. Heritability and shared genetic factors for symptoms of anxiety and depression in a brazilian family-based cohort, the baependI study. European neuropsychopharmacology. 2017 ; 27 S319.[citado 2024 nov. 14 ]
Vancouver
Taporoski T, Negrão AB, Horimoto ARVR, Duarte NE, Alvim RO, Oliveira CM de, Krieger JE, Von chantz M, Vallada Filho HP, Pereira AC. Heritability and shared genetic factors for symptoms of anxiety and depression in a brazilian family-based cohort, the baependI study. European neuropsychopharmacology. 2017 ; 27 S319.[citado 2024 nov. 14 ]
Artigo de periodico
Proteome analysis of acute kidney injury – Discovery of new predominantly renal candidates for biomarker of kidney disease (2017)
Malagrino, Pamella Araujo; Venturini, Gabriela; Yogi, Patrícia Schneider; Dariolli, Rafael; Padilha, Kallyandra; Kiers, Bianca; Gois, Tamiris Carneiro; Cardozo, Karina helena Morais; Carvalho, Valdemir Melechco; Salgueiro, Jéssica Silva; Girardi, Adriana Castello Costa; Titan, Silvia Maria de Oliveira; Krieger, José Eduardo; Pereira, Alexandre Costa
Source: Journal of proteomics. Unidade: FM
Subjects: BIOMARCADORES, NEFROPATIAS, ISQUEMIA, RIM
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ABNT
MALAGRINO, Pamella Araujo et al. Proteome analysis of acute kidney injury – Discovery of new predominantly renal candidates for biomarker of kidney disease. Journal of proteomics, v. 151, p. 66-73, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.jprot.2016.05.016. Acesso em: 14 nov. 2024.
APA
Malagrino, P. A., Venturini, G., Yogi, P. S., Dariolli, R., Padilha, K., Kiers, B., et al. (2017). Proteome analysis of acute kidney injury – Discovery of new predominantly renal candidates for biomarker of kidney disease. Journal of proteomics, 151, 66-73. doi:10.1016/j.jprot.2016.05.016
NLM
Malagrino PA, Venturini G, Yogi PS, Dariolli R, Padilha K, Kiers B, Gois TC, Cardozo K helena M, Carvalho VM, Salgueiro JS, Girardi ACC, Titan SM de O, Krieger JE, Pereira AC. Proteome analysis of acute kidney injury – Discovery of new predominantly renal candidates for biomarker of kidney disease [Internet]. Journal of proteomics. 2017 ; 151 66-73.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.jprot.2016.05.016
Vancouver
Malagrino PA, Venturini G, Yogi PS, Dariolli R, Padilha K, Kiers B, Gois TC, Cardozo K helena M, Carvalho VM, Salgueiro JS, Girardi ACC, Titan SM de O, Krieger JE, Pereira AC. Proteome analysis of acute kidney injury – Discovery of new predominantly renal candidates for biomarker of kidney disease [Internet]. Journal of proteomics. 2017 ; 151 66-73.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.jprot.2016.05.016
Artigo de periodico
MTRR rs326119 polymorphism is associated with plasma concentrations of homocysteine and cobalamin, but not with congenital heart disease or coronary atherosclerosis in Brazilian patients (2017)
Horita, Melanie; Bueno, Carolina Tosin; Horimoto, Andrea R.; Lemos, Pedro A.; Morandini-Filho, Antonio A.; Krieger, José E.; Santos, Paulo C. J. L.; Pereira, Alexandre C.
Source: International Journal of Cardiology. Heart & Vasculature. Unidade: FM
Subjects: DOENÇAS CARDIOVASCULARES, BRASILEIROS, HOMOCISTEÍNA, VITAMINAS, DOENÇAS CONGÊNITAS
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ABNT
HORITA, Melanie et al. MTRR rs326119 polymorphism is associated with plasma concentrations of homocysteine and cobalamin, but not with congenital heart disease or coronary atherosclerosis in Brazilian patients. International Journal of Cardiology. Heart & Vasculature, v. 14, p. 1-5, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.ijcha.2016.11.004. Acesso em: 14 nov. 2024.
APA
Horita, M., Bueno, C. T., Horimoto, A. R., Lemos, P. A., Morandini-Filho, A. A., Krieger, J. E., et al. (2017). MTRR rs326119 polymorphism is associated with plasma concentrations of homocysteine and cobalamin, but not with congenital heart disease or coronary atherosclerosis in Brazilian patients. International Journal of Cardiology. Heart & Vasculature, 14, 1-5. doi:10.1016/j.ijcha.2016.11.004
NLM
Horita M, Bueno CT, Horimoto AR, Lemos PA, Morandini-Filho AA, Krieger JE, Santos PCJL, Pereira AC. MTRR rs326119 polymorphism is associated with plasma concentrations of homocysteine and cobalamin, but not with congenital heart disease or coronary atherosclerosis in Brazilian patients [Internet]. International Journal of Cardiology. Heart & Vasculature. 2017 ; 14 1-5.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.ijcha.2016.11.004
Vancouver
Horita M, Bueno CT, Horimoto AR, Lemos PA, Morandini-Filho AA, Krieger JE, Santos PCJL, Pereira AC. MTRR rs326119 polymorphism is associated with plasma concentrations of homocysteine and cobalamin, but not with congenital heart disease or coronary atherosclerosis in Brazilian patients [Internet]. International Journal of Cardiology. Heart & Vasculature. 2017 ; 14 1-5.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.ijcha.2016.11.004
Artigo de periodico
Allogeneic pASC transplantation in humanized pigs attenuates cardiac remodeling post-myocardial infarction (2017)
Dariolli, Rafael; Naghetini, Marcus V.; Marques, Euclydes F.; Takimura, Celso K.; Jensen, Leonardo S.; Kiers, Bianca; Tsutsui, Jeane M.; Mathias Jr., Wilson; Lemos Neto, Pedro A; Krieger, Jose E.
Source: PLOS ONE. Unidade: FM
Subjects: CO-TERAPIA, RATOS, MEDICAÇÃO INTRAVENOSA, DOENÇAS CARDÍACAS
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ABNT
DARIOLLI, Rafael et al. Allogeneic pASC transplantation in humanized pigs attenuates cardiac remodeling post-myocardial infarction. PLOS ONE, v. 12, n. 4, p. 21 , 2017Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0176412. Acesso em: 14 nov. 2024.
APA
Dariolli, R., Naghetini, M. V., Marques, E. F., Takimura, C. K., Jensen, L. S., Kiers, B., et al. (2017). Allogeneic pASC transplantation in humanized pigs attenuates cardiac remodeling post-myocardial infarction. PLOS ONE, 12( 4), 21 . doi:10.1371/journal.pone.0176412
NLM
Dariolli R, Naghetini MV, Marques EF, Takimura CK, Jensen LS, Kiers B, Tsutsui JM, Mathias Jr. W, Lemos Neto PA, Krieger JE. Allogeneic pASC transplantation in humanized pigs attenuates cardiac remodeling post-myocardial infarction [Internet]. PLOS ONE. 2017 ; 12( 4): 21 .[citado 2024 nov. 14 ] Available from: https://doi.org/10.1371/journal.pone.0176412
Vancouver
Dariolli R, Naghetini MV, Marques EF, Takimura CK, Jensen LS, Kiers B, Tsutsui JM, Mathias Jr. W, Lemos Neto PA, Krieger JE. Allogeneic pASC transplantation in humanized pigs attenuates cardiac remodeling post-myocardial infarction [Internet]. PLOS ONE. 2017 ; 12( 4): 21 .[citado 2024 nov. 14 ] Available from: https://doi.org/10.1371/journal.pone.0176412
Artigo de periodico
ACE-modulated adiposity is related to higher energy expenditure and independent of lipolysis and glucose incorporation into lipids in adipocytes (2017)
Fonseca-Alaniz, Miriam Helena ; Higa, Talita Sayuri; Ferraz-de-Camposo Tarcila Beatriz ; Takada, Julie; Orres-Leal, Francisco Leonardo; Evangelista, Fabiana Sant'Anna ; Lima, Fabio Bessa ; Krieger, José Eduardo
Source: Physiological genomics. Unidades: FM, ICB, EACH
Subjects: ADIPOSIDADE, ANGIOTENSINAS, RATOS, INSUFICIÊNCIA RENAL CRÔNICA, RESISTÊNCIA À INSULINA, FISIOLOGIA
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ABNT
FONSECA-ALANIZ, Miriam Helena et al. ACE-modulated adiposity is related to higher energy expenditure and independent of lipolysis and glucose incorporation into lipids in adipocytes. Physiological genomics, v. 49, n. 12, p. 712-721, 2017Tradução . . Disponível em: https://doi.org/10.1152/physiolgenomics.00056.2017. Acesso em: 14 nov. 2024.
APA
Fonseca-Alaniz, M. H., Higa, T. S., Ferraz-de-Camposo Tarcila Beatriz,, Takada, J., Orres-Leal, F. L., Evangelista, F. S. 'A., et al. (2017). ACE-modulated adiposity is related to higher energy expenditure and independent of lipolysis and glucose incorporation into lipids in adipocytes. Physiological genomics, 49( 12), 712-721. doi:10.1152/physiolgenomics.00056.2017
NLM
Fonseca-Alaniz MH, Higa TS, Ferraz-de-Camposo Tarcila Beatriz, Takada J, Orres-Leal FL, Evangelista FS'A, Lima FB, Krieger JE. ACE-modulated adiposity is related to higher energy expenditure and independent of lipolysis and glucose incorporation into lipids in adipocytes [Internet]. Physiological genomics. 2017 ; 49( 12): 712-721.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1152/physiolgenomics.00056.2017
Vancouver
Fonseca-Alaniz MH, Higa TS, Ferraz-de-Camposo Tarcila Beatriz, Takada J, Orres-Leal FL, Evangelista FS'A, Lima FB, Krieger JE. ACE-modulated adiposity is related to higher energy expenditure and independent of lipolysis and glucose incorporation into lipids in adipocytes [Internet]. Physiological genomics. 2017 ; 49( 12): 712-721.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1152/physiolgenomics.00056.2017
Artigo de periodico
-318C/T polymorphism of the CTLA-4 gene is an independent risk factor for RBC alloimmunization among sickle cell disease patients (2017)
Oliveira, V. B.; Dezan, M. R; Gomes, F. C. A; Gualandro, Sandra Fátima Menosi; Krieger, José Eduardo; Pereira, A. C; Marsiglia, J. D; Levi, J. E; Rocha, Vanderson Geraldo; Mendrone Junior, A; Sabino, Ester Cerdeira; Dinardo, C. L
Source: International journal of immunogenetics. Unidade: FM
Subjects: POLIMORFISMO, ANEMIA FALCIFORME, TRANSFUSÃO DE SANGUE, ANTICORPOS
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ABNT
OLIVEIRA, V. B. et al. -318C/T polymorphism of the CTLA-4 gene is an independent risk factor for RBC alloimmunization among sickle cell disease patients. International journal of immunogenetics, v. 44, n. 5, p. 219-224, 2017Tradução . . Disponível em: https://doi.org/10.1111/iji.12334. Acesso em: 14 nov. 2024.
APA
Oliveira, V. B., Dezan, M. R., Gomes, F. C. A., Gualandro, S. F. M., Krieger, J. E., Pereira, A. C., et al. (2017). -318C/T polymorphism of the CTLA-4 gene is an independent risk factor for RBC alloimmunization among sickle cell disease patients. International journal of immunogenetics, 44( 5), 219-224. doi:10.1111/iji.12334
NLM
Oliveira VB, Dezan MR, Gomes FCA, Gualandro SFM, Krieger JE, Pereira AC, Marsiglia JD, Levi JE, Rocha VG, Mendrone Junior A, Sabino EC, Dinardo CL. -318C/T polymorphism of the CTLA-4 gene is an independent risk factor for RBC alloimmunization among sickle cell disease patients [Internet]. International journal of immunogenetics. 2017 ; 44( 5): 219-224.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1111/iji.12334
Vancouver
Oliveira VB, Dezan MR, Gomes FCA, Gualandro SFM, Krieger JE, Pereira AC, Marsiglia JD, Levi JE, Rocha VG, Mendrone Junior A, Sabino EC, Dinardo CL. -318C/T polymorphism of the CTLA-4 gene is an independent risk factor for RBC alloimmunization among sickle cell disease patients [Internet]. International journal of immunogenetics. 2017 ; 44( 5): 219-224.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1111/iji.12334
Artigo de periodico
Early postnatal cardiomyocyte proliferation requires high oxidative energy metabolism (2017)
Carvalho, Ana Elisa Teófilo Saturi de; Bassaneze, Vinicius; Forni, Maria Fernanda Pereira de Araújo Demonte; Keusseyan, Aline Alfonso; Kowaltowski, Alicia Juliana ; Krieger, José Eduardo
Source: Scientific Reports. Unidades: IQ, FM
Assunto: PROLIFERAÇÃO CELULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CARVALHO, Ana Elisa Teófilo Saturi de et al. Early postnatal cardiomyocyte proliferation requires high oxidative energy metabolism. Scientific Reports, v. 7, p. 1-11 art. 15434, 2017Tradução . . Disponível em: https://doi.org/10.1038/s41598-017-15656-3. Acesso em: 14 nov. 2024.
APA
Carvalho, A. E. T. S. de, Bassaneze, V., Forni, M. F. P. de A. D., Keusseyan, A. A., Kowaltowski, A. J., & Krieger, J. E. (2017). Early postnatal cardiomyocyte proliferation requires high oxidative energy metabolism. Scientific Reports, 7, 1-11 art. 15434. doi:10.1038/s41598-017-15656-3
NLM
Carvalho AETS de, Bassaneze V, Forni MFP de AD, Keusseyan AA, Kowaltowski AJ, Krieger JE. Early postnatal cardiomyocyte proliferation requires high oxidative energy metabolism [Internet]. Scientific Reports. 2017 ; 7 1-11 art. 15434.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1038/s41598-017-15656-3
Vancouver
Carvalho AETS de, Bassaneze V, Forni MFP de AD, Keusseyan AA, Kowaltowski AJ, Krieger JE. Early postnatal cardiomyocyte proliferation requires high oxidative energy metabolism [Internet]. Scientific Reports. 2017 ; 7 1-11 art. 15434.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1038/s41598-017-15656-3
Artigo de periodico
Beta-arrestin is critical for early shear stress-induced Akt/eNOS activation in human vascular endothelial cells (2017)
Carneiro, Ana Paula; Alaniz, Miriam Helena Fonseca; Dallan, Luís Alberto Oliveira; Miyakawa, Ayumi Aurea; Krieger, José Eduardo
Source: Biochemical and biophysical research communications. Unidade: FM
Subjects: PROTEÍNAS G, ESTRESSE OXIDATIVO, CÉLULAS ENDOTELIAIS, ÓXIDO NÍTRICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CARNEIRO, Ana Paula et al. Beta-arrestin is critical for early shear stress-induced Akt/eNOS activation in human vascular endothelial cells. Biochemical and biophysical research communications, v. 483, n. 01, p. 71-80, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.bbrc.2017.01.003. Acesso em: 14 nov. 2024.
APA
Carneiro, A. P., Alaniz, M. H. F., Dallan, L. A. O., Miyakawa, A. A., & Krieger, J. E. (2017). Beta-arrestin is critical for early shear stress-induced Akt/eNOS activation in human vascular endothelial cells. Biochemical and biophysical research communications, 483( 01), 71-80. doi:10.1016/j.bbrc.2017.01.003
NLM
Carneiro AP, Alaniz MHF, Dallan LAO, Miyakawa AA, Krieger JE. Beta-arrestin is critical for early shear stress-induced Akt/eNOS activation in human vascular endothelial cells [Internet]. Biochemical and biophysical research communications. 2017 ; 483( 01): 71-80.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.bbrc.2017.01.003
Vancouver
Carneiro AP, Alaniz MHF, Dallan LAO, Miyakawa AA, Krieger JE. Beta-arrestin is critical for early shear stress-induced Akt/eNOS activation in human vascular endothelial cells [Internet]. Biochemical and biophysical research communications. 2017 ; 483( 01): 71-80.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.bbrc.2017.01.003
Artigo de periodico
RHD and RHCE genotyping by next-generation sequencing is an effective strategy to identify molecular variants within sickle cell disease patients (2017)
Dezana, Marcia R.; Ribeiro, Ingrid Helena; Oliveira, Valéria B.; Vieira, Juliana B.; Gomes, Francisco C.; Franco, Lucas A. M.; Varuzza, Leonardo; Ribeiro, Roberto; Chinoca, Karen Ziza; Levi, José Eduardo; Krieger, José Eduardo; Pereira, Alexandre Costa; Gualandro, Sandra F.M.; Rocha, Vanderson G.; Mendrone-Junior,Alfredo; Sabino, Ester Cerdeira; Dinardo, Carla Luana
Source: Blood Cells, Molecules, and Diseases. Unidade: FM
Subjects: GENÓTIPOS, TÉCNICAS CITOLÓGICAS, REAÇÃO EM CADEIA POR POLIMERASE, TRANSFUSÃO DE SANGUE, SEQUENCIAMENTO GENÉTICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DEZANA, Marcia R. et al. RHD and RHCE genotyping by next-generation sequencing is an effective strategy to identify molecular variants within sickle cell disease patients. Blood Cells, Molecules, and Diseases, v. 65, n. 1, p. 8-15, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.bcmd.2017.03.014. Acesso em: 14 nov. 2024.
APA
Dezana, M. R., Ribeiro, I. H., Oliveira, V. B., Vieira, J. B., Gomes, F. C., Franco, L. A. M., et al. (2017). RHD and RHCE genotyping by next-generation sequencing is an effective strategy to identify molecular variants within sickle cell disease patients. Blood Cells, Molecules, and Diseases, 65( 1), 8-15. doi:10.1016/j.bcmd.2017.03.014
NLM
Dezana MR, Ribeiro IH, Oliveira VB, Vieira JB, Gomes FC, Franco LAM, Varuzza L, Ribeiro R, Chinoca KZ, Levi JE, Krieger JE, Pereira AC, Gualandro SFM, Rocha VG, Mendrone-Junior A, Sabino EC, Dinardo CL. RHD and RHCE genotyping by next-generation sequencing is an effective strategy to identify molecular variants within sickle cell disease patients [Internet]. Blood Cells, Molecules, and Diseases. 2017 ; 65( 1): 8-15.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.bcmd.2017.03.014
Vancouver
Dezana MR, Ribeiro IH, Oliveira VB, Vieira JB, Gomes FC, Franco LAM, Varuzza L, Ribeiro R, Chinoca KZ, Levi JE, Krieger JE, Pereira AC, Gualandro SFM, Rocha VG, Mendrone-Junior A, Sabino EC, Dinardo CL. RHD and RHCE genotyping by next-generation sequencing is an effective strategy to identify molecular variants within sickle cell disease patients [Internet]. Blood Cells, Molecules, and Diseases. 2017 ; 65( 1): 8-15.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.bcmd.2017.03.014
Artigo de periodico
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation (2017)
Christophersen, Ingrid E.; Rienstra, Michiel; Roselli, Carolina; Yin, Xiaoyan; Geelhoed, Bastiaan; Barnard, John; Lin, Honghuang; Arking, Dan E.; Smith, Albert V.; Albert, Christine M.; Chaffin, Mark; Tucker, Nathan R.; Li, Molong; Klarin, Derek; Bihlmeyer, Nathan A.; Low, Siew-Kee; Weeke, Peter E.; Nurasyid, Martina Müller; Smith, J. Gustav; Brody, Jennifer A.; Niemeijer, Maartje N; Dörr, Marcus; Trompet, Stella; Huffman, Jennifer; Gustafsson, Stefan; Schurmann, Claudia; Kleber, Marcus E.; Lyytikäinen, Leo-Pekka; Seppälä, Ilkka; Malik, Rainer; Horimoto, Andrea R. V; Perez, Marco; Sinisalo, Juha; Aeschbacher, Stefanie; Theriault, Sébastien; Yao, Jie; Radmanesh, Farid; Teumer, Alexander; Choi, Seung Hoan; Weng, Lu-Chen; Clauss, Sebastian; Deo, Rajat; Rader, Daniel J; Shah, Svati H; Sun, Albert; Hopewell, Jemma C.; Debette, Stephanie; Chauhan, Ganesh; Yang, Qiong; Worral, Bradford B; Paré, Guillaume; Kamatani, Yoichiro; Hagemeijer, Yanick P; Verweij, Niek; Siland, Joylene E; Kubo, Michiaki; Smith, Jonathan D; Wagoner, David R. Van; Bis, Joshua C; Perz, Siegfried; Psaty, Bruce M; Ridker, Paul M; Magnani, Jared W; Harris, Tamara B; Launer, Lenore J; Shoemaker, M. Benjamin; Padmanabhan, Sandosh; Haessler, Jeffrey; Bartz, Traci M; Waldenberger, Melanie; Lichtner, Peter; Krieger, José Eduardo; Kähönen, Mika; Risch, Lorenz; Mansur, Alfredo José; Peters, Annette; Smith, Blair H; Lind, Lars; Scott, Stuart A; Lu, Yingchang; Bottinger, Erwin B; Hernesniemi, Jussi; Lindgren, Cecilia M; Wong, Jorge A; Huang, Jie; Eskola, Markku; Morris, Andrew P; Ford, Ian; Reiner, Alex P; Delgado, Graciela; Yen, Lin Y; Chen, Yii-Der Ida; Sandhu, Roopinder; Li, Man; Boerwinkle, Eric; Eisele, Lewin; Lannfelt, Lars; Rost, Natalia; Anderson, Christopher D; Taylor, Kent D; Campbell, Archie; Magnusson, Patrick K; Porteous, David; Hoking, Lynne J; Vlachopoulou, Efthymia; Pedersen, Nancy L; Nikus, Kjell; Melander, Marju Orho; Hamsten, Anders; Heeringa, Jan; Denny, Joshua C; Kriebel, Jennifer; Darbar, Dawood; Cheh, Christopher Newton; Shaffer,Christian; Macfarlane, Peter W; Heimbach, Stefanie Heilmann; Almgren, Peter; Huang, Paul L.; Sotoodehnia, Nona; Soliman, Elsayed Z; Uitterlinden, Andre G; Hofman, Albert; Franco, Oscar H; Völker, Uwe; Jöckel, Karl-Heinz; Sinner,Moritz F; Lin, Henry J; Guo, Xiuqing; Dichgans, Martin; Ingelsson, Erik; Kooperberg, Charles; Melander, Olle; Loos, Ruth J. F; Laurikka, Jari; Conen, David; Rosand, Jonathan; Harst, Pim van der; Lokki, Marja-Liisa; Kathiresan, Sekar; Pereira, Alexandre; Jukema, J. Wouter; Hayward, Caroline; Rotter, Jerome I; März, Winfried; Lehtimäki, Terho; Stricker, Bruno H; Chung, Mina K; Felix, Stephan B; Gudnason, Vilmundur; Alonso, Alvaro; Roden, Dan M; Kääb, Stefan; Chasman, Daniel I; Heckbert, Susan R; Benjamin, Emelia J; Tanaka, Toshihiro; Lunetta, Kathryn L; Lubitz, Steven A; Ellinor, Patrick T
Source: Nature Genetics. Unidade: FM
Subjects: FIBRILAÇÃO ATRIAL, METANÁLISE, DOENÇAS CARDIOVASCULARES, GENOMAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CHRISTOPHERSEN, Ingrid E. et al. Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. Nature Genetics, v. 49, n. 6, p. 946-952, 2017Tradução . . Disponível em: https://doi.org/10.1038/ng.3843. Acesso em: 14 nov. 2024.
APA
Christophersen, I. E., Rienstra, M., Roselli, C., Yin, X., Geelhoed, B., Barnard, J., et al. (2017). Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. Nature Genetics, 49( 6), 946-952. doi:10.1038/ng.3843
NLM
Christophersen IE, Rienstra M, Roselli C, Yin X, Geelhoed B, Barnard J, Lin H, Arking DE, Smith AV, Albert CM, Chaffin M, Tucker NR, Li M, Klarin D, Bihlmeyer NA, Low S-K, Weeke PE, Nurasyid MM, Smith JG, Brody JA, Niemeijer MN, Dörr M, Trompet S, Huffman J, Gustafsson S, Schurmann C, Kleber ME, Lyytikäinen L-P, Seppälä I, Malik R, Horimoto ARV, Perez M, Sinisalo J, Aeschbacher S, Theriault S, Yao J, Radmanesh F, Teumer A, Choi SH, Weng L-C, Clauss S, Deo R, Rader DJ, Shah SH, Sun A, Hopewell JC, Debette S, Chauhan G, Yang Q, Worral BB, Paré G, Kamatani Y, Hagemeijer YP, Verweij N, Siland JE, Kubo M, Smith JD, Wagoner DRV, Bis JC, Perz S, Psaty BM, Ridker PM, Magnani JW, Harris TB, Launer LJ, Shoemaker MB, Padmanabhan S, Haessler J, Bartz TM, Waldenberger M, Lichtner P, Krieger JE, Kähönen M, Risch L, Mansur AJ, Peters A, Smith BH, Lind L, Scott SA, Lu Y, Bottinger EB, Hernesniemi J, Lindgren CM, Wong JA, Huang J, Eskola M, Morris AP, Ford I, Reiner AP, Delgado G, Yen LY, Chen Y-DI, Sandhu R, Li M, Boerwinkle E, Eisele L, Lannfelt L, Rost N, Anderson CD, Taylor KD, Campbell A, Magnusson PK, Porteous D, Hoking LJ, Vlachopoulou E, Pedersen NL, Nikus K, Melander MO, Hamsten A, Heeringa J, Denny JC, Kriebel J, Darbar D, Cheh CN, Shaffer C, Macfarlane PW, Heimbach SH, Almgren P, Huang PL, Sotoodehnia N, Soliman EZ, Uitterlinden AG, Hofman A, Franco OH, Völker U, Jöckel K-H, Sinner MF, Lin HJ, Guo X, Dichgans M, Ingelsson E, Kooperberg C, Melander O, Loos RJF, Laurikka J, Conen D, Rosand J, Harst P van der, Lokki M-L, Kathiresan S, Pereira A, Jukema JW, Hayward C, Rotter JI, März W, Lehtimäki T, Stricker BH, Chung MK, Felix SB, Gudnason V, Alonso A, Roden DM, Kääb S, Chasman DI, Heckbert SR, Benjamin EJ, Tanaka T, Lunetta KL, Lubitz SA, Ellinor PT. Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation [Internet]. Nature Genetics. 2017 ; 49( 6): 946-952.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1038/ng.3843
Vancouver
Christophersen IE, Rienstra M, Roselli C, Yin X, Geelhoed B, Barnard J, Lin H, Arking DE, Smith AV, Albert CM, Chaffin M, Tucker NR, Li M, Klarin D, Bihlmeyer NA, Low S-K, Weeke PE, Nurasyid MM, Smith JG, Brody JA, Niemeijer MN, Dörr M, Trompet S, Huffman J, Gustafsson S, Schurmann C, Kleber ME, Lyytikäinen L-P, Seppälä I, Malik R, Horimoto ARV, Perez M, Sinisalo J, Aeschbacher S, Theriault S, Yao J, Radmanesh F, Teumer A, Choi SH, Weng L-C, Clauss S, Deo R, Rader DJ, Shah SH, Sun A, Hopewell JC, Debette S, Chauhan G, Yang Q, Worral BB, Paré G, Kamatani Y, Hagemeijer YP, Verweij N, Siland JE, Kubo M, Smith JD, Wagoner DRV, Bis JC, Perz S, Psaty BM, Ridker PM, Magnani JW, Harris TB, Launer LJ, Shoemaker MB, Padmanabhan S, Haessler J, Bartz TM, Waldenberger M, Lichtner P, Krieger JE, Kähönen M, Risch L, Mansur AJ, Peters A, Smith BH, Lind L, Scott SA, Lu Y, Bottinger EB, Hernesniemi J, Lindgren CM, Wong JA, Huang J, Eskola M, Morris AP, Ford I, Reiner AP, Delgado G, Yen LY, Chen Y-DI, Sandhu R, Li M, Boerwinkle E, Eisele L, Lannfelt L, Rost N, Anderson CD, Taylor KD, Campbell A, Magnusson PK, Porteous D, Hoking LJ, Vlachopoulou E, Pedersen NL, Nikus K, Melander MO, Hamsten A, Heeringa J, Denny JC, Kriebel J, Darbar D, Cheh CN, Shaffer C, Macfarlane PW, Heimbach SH, Almgren P, Huang PL, Sotoodehnia N, Soliman EZ, Uitterlinden AG, Hofman A, Franco OH, Völker U, Jöckel K-H, Sinner MF, Lin HJ, Guo X, Dichgans M, Ingelsson E, Kooperberg C, Melander O, Loos RJF, Laurikka J, Conen D, Rosand J, Harst P van der, Lokki M-L, Kathiresan S, Pereira A, Jukema JW, Hayward C, Rotter JI, März W, Lehtimäki T, Stricker BH, Chung MK, Felix SB, Gudnason V, Alonso A, Roden DM, Kääb S, Chasman DI, Heckbert SR, Benjamin EJ, Tanaka T, Lunetta KL, Lubitz SA, Ellinor PT. Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation [Internet]. Nature Genetics. 2017 ; 49( 6): 946-952.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1038/ng.3843
Artigo de periodico
Non-HDL cholesterol is a good predictor of the risk of increased arterial stiffness in postmenopausal women in an urban Brazilian population (2017)
Alvim, Rafael de Oliveira; Mourao-Junior, Carlos Alberto; Magalhães, Géssica Lopes; Oliveira, Camila Maciel de; Krieger, José Eduardo; Mill, José Geraldo; Pereira, Alexandre Costa
Source: Clinics. Unidade: FM
Subjects: FATORES DE RISCO, MENOPAUSA, DISLIPIDEMIAS, COLESTEROL, POPULAÇÃO URBANA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ALVIM, Rafael de Oliveira et al. Non-HDL cholesterol is a good predictor of the risk of increased arterial stiffness in postmenopausal women in an urban Brazilian population. Clinics, v. 72, n. 2, p. 106-110, 2017Tradução . . Disponível em: https://doi.org/10.6061/clinics/2017(02)07. Acesso em: 14 nov. 2024.
APA
Alvim, R. de O., Mourao-Junior, C. A., Magalhães, G. L., Oliveira, C. M. de, Krieger, J. E., Mill, J. G., & Pereira, A. C. (2017). Non-HDL cholesterol is a good predictor of the risk of increased arterial stiffness in postmenopausal women in an urban Brazilian population. Clinics, 72( 2), 106-110. doi:10.6061/clinics/2017(02)07
NLM
Alvim R de O, Mourao-Junior CA, Magalhães GL, Oliveira CM de, Krieger JE, Mill JG, Pereira AC. Non-HDL cholesterol is a good predictor of the risk of increased arterial stiffness in postmenopausal women in an urban Brazilian population [Internet]. Clinics. 2017 ; 72( 2): 106-110.[citado 2024 nov. 14 ] Available from: https://doi.org/10.6061/clinics/2017(02)07
Vancouver
Alvim R de O, Mourao-Junior CA, Magalhães GL, Oliveira CM de, Krieger JE, Mill JG, Pereira AC. Non-HDL cholesterol is a good predictor of the risk of increased arterial stiffness in postmenopausal women in an urban Brazilian population [Internet]. Clinics. 2017 ; 72( 2): 106-110.[citado 2024 nov. 14 ] Available from: https://doi.org/10.6061/clinics/2017(02)07
Artigo de periodico
Amerindian (but not African or European) ancestry is significantly associated with diurnal preference within an admixed Brazilian population (2017)
Egan, Kieren J.; Santos, Hadassa Campos; Beijamini, Felipe; Duarte, Nubia Esteban; Horimoto, Andréa Roseli Vançan Russo; Taporoski, Tâmara Pessanha; Vallada Filho, Homero Pinto; Negrão, André Brooking; Krieger, José Eduardo; Pedrazzoli Neto, Mário; Knutson, Kristen L.; Pereira, Alexandre Costa; Schantz, Malcolm von
Source: Chronobiology International. Unidades: EACH, FM
Subjects: RITMO CIRCADIANO, RITMOS BIOLÓGICOS, ANCESTRAIS, BRASILEIROS, COSTUMES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
EGAN, Kieren J. et al. Amerindian (but not African or European) ancestry is significantly associated with diurnal preference within an admixed Brazilian population. Chronobiology International, v. 34, n. 2, p. 262-272, 2017Tradução . . Disponível em: https://doi.org/10.1080/07420528.2016.1265979. Acesso em: 14 nov. 2024.
APA
Egan, K. J., Santos, H. C., Beijamini, F., Duarte, N. E., Horimoto, A. R. V. R., Taporoski, T. P., et al. (2017). Amerindian (but not African or European) ancestry is significantly associated with diurnal preference within an admixed Brazilian population. Chronobiology International, 34( 2), 262-272. doi:10.1080/07420528.2016.1265979
NLM
Egan KJ, Santos HC, Beijamini F, Duarte NE, Horimoto ARVR, Taporoski TP, Vallada Filho HP, Negrão AB, Krieger JE, Pedrazzoli Neto M, Knutson KL, Pereira AC, Schantz M von. Amerindian (but not African or European) ancestry is significantly associated with diurnal preference within an admixed Brazilian population [Internet]. Chronobiology International. 2017 ; 34( 2): 262-272.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1080/07420528.2016.1265979
Vancouver
Egan KJ, Santos HC, Beijamini F, Duarte NE, Horimoto ARVR, Taporoski TP, Vallada Filho HP, Negrão AB, Krieger JE, Pedrazzoli Neto M, Knutson KL, Pereira AC, Schantz M von. Amerindian (but not African or European) ancestry is significantly associated with diurnal preference within an admixed Brazilian population [Internet]. Chronobiology International. 2017 ; 34( 2): 262-272.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1080/07420528.2016.1265979
Artigo de periodico
Online extraction of antihypertensive drugs and their metabolites from untreated human serum samples using restricted access carbon nanotubes in a column switching liquid chromatography system (2017)
Faria, Henrique Dipe de; Bueno, Carolina Tosin; Krieger, Jose Eduardo; Krieger, Eduardo Moacyr; Pereira, Alexandre Costa; Santos, Paulo Caleb Júnior Lima; Figueiredo, Eduardo Costa
Source: Journal of chromatography a. Unidade: FM
Subjects: FÁRMACOS, NANOTUBOS DE CARBONO, HIPERTENSÃO, CROMATOGRAFIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FARIA, Henrique Dipe de et al. Online extraction of antihypertensive drugs and their metabolites from untreated human serum samples using restricted access carbon nanotubes in a column switching liquid chromatography system. Journal of chromatography a, v. 1528, p. 41-52, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.chroma.2017.10.072. Acesso em: 14 nov. 2024.
APA
Faria, H. D. de, Bueno, C. T., Krieger, J. E., Krieger, E. M., Pereira, A. C., Santos, P. C. J. L., & Figueiredo, E. C. (2017). Online extraction of antihypertensive drugs and their metabolites from untreated human serum samples using restricted access carbon nanotubes in a column switching liquid chromatography system. Journal of chromatography a, 1528, 41-52. doi:10.1016/j.chroma.2017.10.072
NLM
Faria HD de, Bueno CT, Krieger JE, Krieger EM, Pereira AC, Santos PCJL, Figueiredo EC. Online extraction of antihypertensive drugs and their metabolites from untreated human serum samples using restricted access carbon nanotubes in a column switching liquid chromatography system [Internet]. Journal of chromatography a. 2017 ; 1528 41-52.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.chroma.2017.10.072
Vancouver
Faria HD de, Bueno CT, Krieger JE, Krieger EM, Pereira AC, Santos PCJL, Figueiredo EC. Online extraction of antihypertensive drugs and their metabolites from untreated human serum samples using restricted access carbon nanotubes in a column switching liquid chromatography system [Internet]. Journal of chromatography a. 2017 ; 1528 41-52.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.chroma.2017.10.072

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