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Artigo de periodico
Genome-wide association study of early ischaemic stroke risk in Brazilian individuals with sickle cell disease implicates ADAMTS2 and CDK18 and uncovers novel loci (2023)
Earley, Eric Jay ; Kelly, Shannon ; Fang, Fang ; Alencar, Cecilia Salete ; Rodrigues, Daniela de Oliveira Werneck ; Cruz, Dahra Teles Soares; Flanagan, Jonathan M; Ware, Russell E ; Zhang, Xu ; Gordeuk, Victor ; Sabino, Ester Cerdeira ; Dinardo, Carla Luana
Source: British journal of haematology. Unidade: FM
Subjects: ACIDENTE VASCULAR CEREBRAL, ANEMIA FALCIFORME, ULTRASSONOGRAFIA DOPPLER TRANSCRANIANA, DIAGNÓSTICO POR IMAGEM
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ABNT
EARLEY, Eric Jay et al. Genome-wide association study of early ischaemic stroke risk in Brazilian individuals with sickle cell disease implicates ADAMTS2 and CDK18 and uncovers novel loci. British journal of haematology, v. 201, n. 2, p. 343-352, 2023Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/53928. Acesso em: 03 nov. 2024.
APA
Earley, E. J., Kelly, S., Fang, F., Alencar, C. S., Rodrigues, D. de O. W., Cruz, D. T. S., et al. (2023). Genome-wide association study of early ischaemic stroke risk in Brazilian individuals with sickle cell disease implicates ADAMTS2 and CDK18 and uncovers novel loci. British journal of haematology, 201( 2), 343-352. doi:10.1111/bjh.18637
NLM
Earley EJ, Kelly S, Fang F, Alencar CS, Rodrigues D de OW, Cruz DTS, Flanagan JM, Ware RE, Zhang X, Gordeuk V, Sabino EC, Dinardo CL. Genome-wide association study of early ischaemic stroke risk in Brazilian individuals with sickle cell disease implicates ADAMTS2 and CDK18 and uncovers novel loci [Internet]. British journal of haematology. 2023 ; 201( 2): 343-352.[citado 2024 nov. 03 ] Available from: https://observatorio.fm.usp.br/handle/OPI/53928
Vancouver
Earley EJ, Kelly S, Fang F, Alencar CS, Rodrigues D de OW, Cruz DTS, Flanagan JM, Ware RE, Zhang X, Gordeuk V, Sabino EC, Dinardo CL. Genome-wide association study of early ischaemic stroke risk in Brazilian individuals with sickle cell disease implicates ADAMTS2 and CDK18 and uncovers novel loci [Internet]. British journal of haematology. 2023 ; 201( 2): 343-352.[citado 2024 nov. 03 ] Available from: https://observatorio.fm.usp.br/handle/OPI/53928
Artigo de periodico
Effectiveness of strategies to screen for blood donors with RH variants in a mixed population (2020)
Almeida, Fabio Augusto Abreu de; Dezan, Marcia Regina; Oliveira, Valeria Brito; Alencar, Cecilia Salete; Luz, Fabio; Krieger, Jose Eduardo ; Pereira, Alexandre Costa; Sabino, Ester Cerdeira ; Rocha, Vanderson Geraldo ; Mendrone-Junior, Alfredo; Dinardo, Carla Luana
Source: Transfusion and apheresis science. Unidade: FM
Subjects: ANTICORPOS, ANTÍGENOS, FENÓTIPOS, GENÓTIPOS, PACIENTES, DOADORES DE SANGUE
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ABNT
ALMEIDA, Fabio Augusto Abreu de et al. Effectiveness of strategies to screen for blood donors with RH variants in a mixed population. Transfusion and apheresis science, v. 59, n. 2, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.transci.2020.102720. Acesso em: 03 nov. 2024.
APA
Almeida, F. A. A. de, Dezan, M. R., Oliveira, V. B., Alencar, C. S., Luz, F., Krieger, J. E., et al. (2020). Effectiveness of strategies to screen for blood donors with RH variants in a mixed population. Transfusion and apheresis science, 59( 2). doi:10.1016/j.transci.2020.102720
NLM
Almeida FAA de, Dezan MR, Oliveira VB, Alencar CS, Luz F, Krieger JE, Pereira AC, Sabino EC, Rocha VG, Mendrone-Junior A, Dinardo CL. Effectiveness of strategies to screen for blood donors with RH variants in a mixed population [Internet]. Transfusion and apheresis science. 2020 ; 59( 2):[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.transci.2020.102720
Vancouver
Almeida FAA de, Dezan MR, Oliveira VB, Alencar CS, Luz F, Krieger JE, Pereira AC, Sabino EC, Rocha VG, Mendrone-Junior A, Dinardo CL. Effectiveness of strategies to screen for blood donors with RH variants in a mixed population [Internet]. Transfusion and apheresis science. 2020 ; 59( 2):[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.transci.2020.102720
Artigo de periodico
Use of an automated pyrosequencing technique for confirmation of sickle cell disease (2019)
Martino, Camila Cruz de; Alencar, Cecilia Salete; Loureiro, Paula; Carneiro-Proietti, Anna Barbara de Freitas; Maximo, Claudia de Alvarenga; Mota, Rosimere Afonso; Rodrigues, Daniela Oliveira Werneck; Gaburo Junior, Nelson; Kelly, Shannon; Sabino, Ester Cerdeira
Source: PLOS ONE. Unidade: FM
Subjects: CELULOSE, ELETROFORESE, GENÓTIPOS, AGAR
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ABNT
MARTINO, Camila Cruz de et al. Use of an automated pyrosequencing technique for confirmation of sickle cell disease. PLOS ONE, v. 14, n. 12, 2019Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0216020. Acesso em: 03 nov. 2024.
APA
Martino, C. C. de, Alencar, C. S., Loureiro, P., Carneiro-Proietti, A. B. de F., Maximo, C. de A., Mota, R. A., et al. (2019). Use of an automated pyrosequencing technique for confirmation of sickle cell disease. PLOS ONE, 14( 12). doi:10.1371/journal.pone.0216020
NLM
Martino CC de, Alencar CS, Loureiro P, Carneiro-Proietti AB de F, Maximo C de A, Mota RA, Rodrigues DOW, Gaburo Junior N, Kelly S, Sabino EC. Use of an automated pyrosequencing technique for confirmation of sickle cell disease [Internet]. PLOS ONE. 2019 ; 14( 12):[citado 2024 nov. 03 ] Available from: https://doi.org/10.1371/journal.pone.0216020
Vancouver
Martino CC de, Alencar CS, Loureiro P, Carneiro-Proietti AB de F, Maximo C de A, Mota RA, Rodrigues DOW, Gaburo Junior N, Kelly S, Sabino EC. Use of an automated pyrosequencing technique for confirmation of sickle cell disease [Internet]. PLOS ONE. 2019 ; 14( 12):[citado 2024 nov. 03 ] Available from: https://doi.org/10.1371/journal.pone.0216020
Artigo de periodico
High frequency of variant RHD genotypes among donors and patients of mixed origin with serologic weak-D phenotype (2018)
Dezan, Marcia Regina; Oliveira, Valeria B; Gomes, Carolina Nunes; Luz, Fabio; Gallucci, Antonio J; Bonifacio, Silvia L; Alencar, Cecilia Salete; Sabino, Ester C; Pereira, Alexandre C; Krieger, Jose E; Rocha, Vanderson Geraldo
Source: Journal of clinical laboratory analysis. Unidade: FM
Subjects: GENÓTIPOS, DOADORES DE SANGUE, FENÓTIPOS, TRANSFUSÃO DE SANGUE, SISTEMA DO GRUPO SANGUÍNEO RH-HR, TESTES SOROLÓGICOS
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ABNT
DEZAN, Marcia Regina et al. High frequency of variant RHD genotypes among donors and patients of mixed origin with serologic weak-D phenotype. Journal of clinical laboratory analysis, v. 32, n. 9, 2018Tradução . . Disponível em: https://doi.org/10.1002/jcla.22596. Acesso em: 03 nov. 2024.
APA
Dezan, M. R., Oliveira, V. B., Gomes, C. N., Luz, F., Gallucci, A. J., Bonifacio, S. L., et al. (2018). High frequency of variant RHD genotypes among donors and patients of mixed origin with serologic weak-D phenotype. Journal of clinical laboratory analysis, 32( 9). doi:10.1002/jcla.22596
NLM
Dezan MR, Oliveira VB, Gomes CN, Luz F, Gallucci AJ, Bonifacio SL, Alencar CS, Sabino EC, Pereira AC, Krieger JE, Rocha VG. High frequency of variant RHD genotypes among donors and patients of mixed origin with serologic weak-D phenotype [Internet]. Journal of clinical laboratory analysis. 2018 ; 32( 9):[citado 2024 nov. 03 ] Available from: https://doi.org/10.1002/jcla.22596
Vancouver
Dezan MR, Oliveira VB, Gomes CN, Luz F, Gallucci AJ, Bonifacio SL, Alencar CS, Sabino EC, Pereira AC, Krieger JE, Rocha VG. High frequency of variant RHD genotypes among donors and patients of mixed origin with serologic weak-D phenotype [Internet]. Journal of clinical laboratory analysis. 2018 ; 32( 9):[citado 2024 nov. 03 ] Available from: https://doi.org/10.1002/jcla.22596
Artigo de periodico
Methicillin-resistant Staphylococcus aureus carrying SCCmec type II was more frequent than the Brazilian endemic clone as a cause of nosocomial bacteremia (2013)
Caiaffa-Filho, Helio Hehl; Trindade, Priscila A.; Cunha, Paula Gabriela da; Alencar, Cecilia Salete; Prado, Gladys V. B.; Rossi, Flavia; Levin, Anna S.
Source: Diagnostic Microbiology and Infectious Disease. Unidade: FM
Subjects: INFECÇÕES BACTERIANAS, INFECÇÕES ESTAFILOCÓCICAS (EPIDEMIOLOGIA), RESISTÊNCIA MICROBIANA ÀS DROGAS, ATENÇÃO TERCIÁRIA À SAÚDE, INFECÇÃO HOSPITALAR (TERAPIA)
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ABNT
CAIAFFA-FILHO, Helio Hehl et al. Methicillin-resistant Staphylococcus aureus carrying SCCmec type II was more frequent than the Brazilian endemic clone as a cause of nosocomial bacteremia. Diagnostic Microbiology and Infectious Disease, v. 76, n. 4, p. 518-520, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.diagmicrobio.2013.04.024. Acesso em: 03 nov. 2024.
APA
Caiaffa-Filho, H. H., Trindade, P. A., Cunha, P. G. da, Alencar, C. S., Prado, G. V. B., Rossi, F., & Levin, A. S. (2013). Methicillin-resistant Staphylococcus aureus carrying SCCmec type II was more frequent than the Brazilian endemic clone as a cause of nosocomial bacteremia. Diagnostic Microbiology and Infectious Disease, 76( 4), 518-520. doi:10.1016/j.diagmicrobio.2013.04.024
NLM
Caiaffa-Filho HH, Trindade PA, Cunha PG da, Alencar CS, Prado GVB, Rossi F, Levin AS. Methicillin-resistant Staphylococcus aureus carrying SCCmec type II was more frequent than the Brazilian endemic clone as a cause of nosocomial bacteremia [Internet]. Diagnostic Microbiology and Infectious Disease. 2013 ; 76( 4): 518-520.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.diagmicrobio.2013.04.024
Vancouver
Caiaffa-Filho HH, Trindade PA, Cunha PG da, Alencar CS, Prado GVB, Rossi F, Levin AS. Methicillin-resistant Staphylococcus aureus carrying SCCmec type II was more frequent than the Brazilian endemic clone as a cause of nosocomial bacteremia [Internet]. Diagnostic Microbiology and Infectious Disease. 2013 ; 76( 4): 518-520.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.diagmicrobio.2013.04.024

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