A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OLIVEIRA, Francine Hehn de et al. Hipotálamo. Bogliolo Patologia. Tradução . Rio de Janeiro: Guanabara Koogan, 2022. . . Acesso em: 01 nov. 2024.
APA
Oliveira, F. H. de, Coutinho, L. M. B., Oliveira, M. da C., Hilbig, A., Pittella, J. E. H., & Zerbini, M. C. N. (2022). Hipotálamo. In Bogliolo Patologia. Rio de Janeiro: Guanabara Koogan.
NLM
Oliveira FH de, Coutinho LMB, Oliveira M da C, Hilbig A, Pittella JEH, Zerbini MCN. Hipotálamo. In: Bogliolo Patologia. Rio de Janeiro: Guanabara Koogan; 2022. [citado 2024 nov. 01 ]
Vancouver
Oliveira FH de, Coutinho LMB, Oliveira M da C, Hilbig A, Pittella JEH, Zerbini MCN. Hipotálamo. In: Bogliolo Patologia. Rio de Janeiro: Guanabara Koogan; 2022. [citado 2024 nov. 01 ]
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PASSAIA, Bárbara dos Santos et al. Stathmin 1 is highly expressed and associated with survival outcome in malignant adrenocortical tumours. Investigational New Drugs, v. 38, p. 899–908, 2020Tradução . . Disponível em: https://doi.org/10.1007/s10637-019-00846-9. Acesso em: 01 nov. 2024.
APA
Passaia, B. dos S., Lima, K., Kremer, J. L., Conceição, B. B. da, Mariani, B. M. de P., Silva, J. C. L. da, et al. (2020). Stathmin 1 is highly expressed and associated with survival outcome in malignant adrenocortical tumours. Investigational New Drugs, 38, 899–908. doi:10.1007/s10637-019-00846-9
NLM
Passaia B dos S, Lima K, Kremer JL, Conceição BB da, Mariani BM de P, Silva JCL da, Zerbini MCN, Fragoso MCBV, Machado Neto JA, Lotfi CFP. Stathmin 1 is highly expressed and associated with survival outcome in malignant adrenocortical tumours [Internet]. Investigational New Drugs. 2020 ; 38 899–908.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1007/s10637-019-00846-9
Vancouver
Passaia B dos S, Lima K, Kremer JL, Conceição BB da, Mariani BM de P, Silva JCL da, Zerbini MCN, Fragoso MCBV, Machado Neto JA, Lotfi CFP. Stathmin 1 is highly expressed and associated with survival outcome in malignant adrenocortical tumours [Internet]. Investigational New Drugs. 2020 ; 38 899–908.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1007/s10637-019-00846-9
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MARIANI, Beatriz Marinho de Paula et al. Allelic Variants of ARMC5 in Patients With Adrenal Incidentalomas and in Patients With Cushing's Syndrome Associated With Bilateral Adrenal Nodules. Frontiers in endocrinology, v. 11, 2020Tradução . . Disponível em: https://doi.org/10.3389/fendo.2020.00036. Acesso em: 01 nov. 2024.
APA
Mariani, B. M. de P., Nishi, M. Y., Wanichi, I. Q., Brondani, V. B., Lacombe, A. M. F., Charchar, H., et al. (2020). Allelic Variants of ARMC5 in Patients With Adrenal Incidentalomas and in Patients With Cushing's Syndrome Associated With Bilateral Adrenal Nodules. Frontiers in endocrinology, 11. doi:10.3389/fendo.2020.00036
NLM
Mariani BM de P, Nishi MY, Wanichi IQ, Brondani VB, Lacombe AMF, Charchar H, Pereira MAA, Srougi V, Zerbini MCN, Mendonca BB de. Allelic Variants of ARMC5 in Patients With Adrenal Incidentalomas and in Patients With Cushing's Syndrome Associated With Bilateral Adrenal Nodules [Internet]. Frontiers in endocrinology. 2020 ; 11[citado 2024 nov. 01 ] Available from: https://doi.org/10.3389/fendo.2020.00036
Vancouver
Mariani BM de P, Nishi MY, Wanichi IQ, Brondani VB, Lacombe AMF, Charchar H, Pereira MAA, Srougi V, Zerbini MCN, Mendonca BB de. Allelic Variants of ARMC5 in Patients With Adrenal Incidentalomas and in Patients With Cushing's Syndrome Associated With Bilateral Adrenal Nodules [Internet]. Frontiers in endocrinology. 2020 ; 11[citado 2024 nov. 01 ] Available from: https://doi.org/10.3389/fendo.2020.00036
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CONCEIÇÃO, Bárbara Brito da et al. ARMC5 mutations are associated with high levels of proliferating cell nuclear antigen and the presence of the serotonin receptor 5HT4R in PMAH nodules. Archives of Endocrinology and Metabolism, v. 64, n. 4, p. 390-401, 2020Tradução . . Disponível em: https://doi.org/10.20945/2359-3997000000236. Acesso em: 01 nov. 2024.
APA
Conceição, B. B. da, Cavalcante, I. P., Kremer, J. L., Auricino, T. B., Bento, E. C., Zerbini, M. C. N., et al. (2020). ARMC5 mutations are associated with high levels of proliferating cell nuclear antigen and the presence of the serotonin receptor 5HT4R in PMAH nodules. Archives of Endocrinology and Metabolism, 64( 4), 390-401. doi:10.20945/2359-3997000000236
NLM
Conceição BB da, Cavalcante IP, Kremer JL, Auricino TB, Bento EC, Zerbini MCN, Fragoso MCBV, Lotfi CFP. ARMC5 mutations are associated with high levels of proliferating cell nuclear antigen and the presence of the serotonin receptor 5HT4R in PMAH nodules [Internet]. Archives of Endocrinology and Metabolism. 2020 ; 64( 4): 390-401.[citado 2024 nov. 01 ] Available from: https://doi.org/10.20945/2359-3997000000236
Vancouver
Conceição BB da, Cavalcante IP, Kremer JL, Auricino TB, Bento EC, Zerbini MCN, Fragoso MCBV, Lotfi CFP. ARMC5 mutations are associated with high levels of proliferating cell nuclear antigen and the presence of the serotonin receptor 5HT4R in PMAH nodules [Internet]. Archives of Endocrinology and Metabolism. 2020 ; 64( 4): 390-401.[citado 2024 nov. 01 ] Available from: https://doi.org/10.20945/2359-3997000000236
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MARCHESI, Raquel F et al. Clinical impact of dysplastic changes in acquired aplastic anemia: a systematic study of bone marrow biopsies in children and adults. Annals of diagnostic pathology, v. 45, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.anndiagpath.2019.151459. Acesso em: 01 nov. 2024.
APA
Marchesi, R. F., Velloso, E. D. R. P., Garanito, M. P., Leal, A. M., Siqueira, S. A. C., Azevedo Neto, R. S. de, et al. (2020). Clinical impact of dysplastic changes in acquired aplastic anemia: a systematic study of bone marrow biopsies in children and adults. Annals of diagnostic pathology, 45. doi:10.1016/j.anndiagpath.2019.151459
NLM
Marchesi RF, Velloso EDRP, Garanito MP, Leal AM, Siqueira SAC, Azevedo Neto RS de, Rocha VG, Zerbini MCN. Clinical impact of dysplastic changes in acquired aplastic anemia: a systematic study of bone marrow biopsies in children and adults [Internet]. Annals of diagnostic pathology. 2020 ; 45[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.anndiagpath.2019.151459
Vancouver
Marchesi RF, Velloso EDRP, Garanito MP, Leal AM, Siqueira SAC, Azevedo Neto RS de, Rocha VG, Zerbini MCN. Clinical impact of dysplastic changes in acquired aplastic anemia: a systematic study of bone marrow biopsies in children and adults [Internet]. Annals of diagnostic pathology. 2020 ; 45[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.anndiagpath.2019.151459
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERREIRA, Cristiane R et al. Genetic Subtypes of Systemic Anaplastic Large Cell Lymphoma Show Distinct Differences in PD-L1 Expression and Regulatory and Cytotoxic T Cells in the Tumor Microenvironment. Applied immunohistochemistry & molecular morphology, v. 28, n. 1, p. 10-16, 2020Tradução . . Disponível em: https://doi.org/10.1097/PAI.0000000000000798. Acesso em: 01 nov. 2024.
APA
Ferreira, C. R., Manohar, V., Zhao, S., Bangs, C. D., Cherry, A., Azevedo Neto, R. S., et al. (2020). Genetic Subtypes of Systemic Anaplastic Large Cell Lymphoma Show Distinct Differences in PD-L1 Expression and Regulatory and Cytotoxic T Cells in the Tumor Microenvironment. Applied immunohistochemistry & molecular morphology, 28( 1), 10-16. doi:10.1097/PAI.0000000000000798
NLM
Ferreira CR, Manohar V, Zhao S, Bangs CD, Cherry A, Azevedo Neto RS, Lage LAPC, Pereira J, Zerbini MCN, Gratzinger D. Genetic Subtypes of Systemic Anaplastic Large Cell Lymphoma Show Distinct Differences in PD-L1 Expression and Regulatory and Cytotoxic T Cells in the Tumor Microenvironment [Internet]. Applied immunohistochemistry & molecular morphology. 2020 ; 28( 1): 10-16.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1097/PAI.0000000000000798
Vancouver
Ferreira CR, Manohar V, Zhao S, Bangs CD, Cherry A, Azevedo Neto RS, Lage LAPC, Pereira J, Zerbini MCN, Gratzinger D. Genetic Subtypes of Systemic Anaplastic Large Cell Lymphoma Show Distinct Differences in PD-L1 Expression and Regulatory and Cytotoxic T Cells in the Tumor Microenvironment [Internet]. Applied immunohistochemistry & molecular morphology. 2020 ; 28( 1): 10-16.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1097/PAI.0000000000000798
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
POLES, Wagner A et al. Targeting the polarization of tumor-associated macrophages and modulating mir-155 expression might be a new approach to treat diffuse large B-cell lymphoma of the elderly. Cancer immunology immunotherapy, v. 68, n. 2, p. 269-282, 2019Tradução . . Disponível em: https://doi.org/10.1007/s00262-018-2273-2. Acesso em: 01 nov. 2024.
APA
Poles, W. A., Nishi, E. E., Oliveira, M. B. de, Eugenio, A. I. P., Andrade, T. A. de, Campos, A. H. F. M., et al. (2019). Targeting the polarization of tumor-associated macrophages and modulating mir-155 expression might be a new approach to treat diffuse large B-cell lymphoma of the elderly. Cancer immunology immunotherapy, 68( 2), 269-282. doi:10.1007/s00262-018-2273-2
NLM
Poles WA, Nishi EE, Oliveira MB de, Eugenio AIP, Andrade TA de, Campos AHFM, Campos Jr. RR de, Vassallo J, Alves AC, Neto CS, Zerbini MCN, Colleoni GWB. Targeting the polarization of tumor-associated macrophages and modulating mir-155 expression might be a new approach to treat diffuse large B-cell lymphoma of the elderly [Internet]. Cancer immunology immunotherapy. 2019 ; 68( 2): 269-282.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1007/s00262-018-2273-2
Vancouver
Poles WA, Nishi EE, Oliveira MB de, Eugenio AIP, Andrade TA de, Campos AHFM, Campos Jr. RR de, Vassallo J, Alves AC, Neto CS, Zerbini MCN, Colleoni GWB. Targeting the polarization of tumor-associated macrophages and modulating mir-155 expression might be a new approach to treat diffuse large B-cell lymphoma of the elderly [Internet]. Cancer immunology immunotherapy. 2019 ; 68( 2): 269-282.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1007/s00262-018-2273-2
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LAGE, Luis Alberto de Padua Covas et al. Absolute monocyte count is a predictor of overall survival and progression-free survival in nodal peripheral T cell lymphoma. Annals of hematology, v. 98, n. 9, p. 2097-2102, 2019Tradução . . Disponível em: https://doi.org/10.1007/s00277-019-03731-w. Acesso em: 01 nov. 2024.
APA
Lage, L. A. de P. C., Hamasaki, D. T., Moreira, F. R., Rocha, V. G., Zerbini, M. C. N., & Pereira, J. (2019). Absolute monocyte count is a predictor of overall survival and progression-free survival in nodal peripheral T cell lymphoma. Annals of hematology, 98( 9), 2097-2102. doi:10.1007/s00277-019-03731-w
NLM
Lage LA de PC, Hamasaki DT, Moreira FR, Rocha VG, Zerbini MCN, Pereira J. Absolute monocyte count is a predictor of overall survival and progression-free survival in nodal peripheral T cell lymphoma [Internet]. Annals of hematology. 2019 ; 98( 9): 2097-2102.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1007/s00277-019-03731-w
Vancouver
Lage LA de PC, Hamasaki DT, Moreira FR, Rocha VG, Zerbini MCN, Pereira J. Absolute monocyte count is a predictor of overall survival and progression-free survival in nodal peripheral T cell lymphoma [Internet]. Annals of hematology. 2019 ; 98( 9): 2097-2102.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1007/s00277-019-03731-w
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERREIRA, Amanda Meneses et al. Clinical spectrum of Li-Fraumeni syndrome/Li-Fraumeni-like syndrome in Brazilian individuals with the TP53 p.R337H mutation. Journal of steroid biochemistry and molecular biology, v. 190, p. 250-255, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.jsbmb.2019.04.011. Acesso em: 01 nov. 2024.
APA
Ferreira, A. M., Brondani, V. B., Helena, V. P., Charchar, H. L. S., Zerbini, M. C. N., Leite, L. A. S., et al. (2019). Clinical spectrum of Li-Fraumeni syndrome/Li-Fraumeni-like syndrome in Brazilian individuals with the TP53 p.R337H mutation. Journal of steroid biochemistry and molecular biology, 190, 250-255. doi:10.1016/j.jsbmb.2019.04.011
NLM
Ferreira AM, Brondani VB, Helena VP, Charchar HLS, Zerbini MCN, Leite LAS, Hoff AO, Xavier ACL, Mendonça BB de, Diz MDPE. Clinical spectrum of Li-Fraumeni syndrome/Li-Fraumeni-like syndrome in Brazilian individuals with the TP53 p.R337H mutation [Internet]. Journal of steroid biochemistry and molecular biology. 2019 ; 190 250-255.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.jsbmb.2019.04.011
Vancouver
Ferreira AM, Brondani VB, Helena VP, Charchar HLS, Zerbini MCN, Leite LAS, Hoff AO, Xavier ACL, Mendonça BB de, Diz MDPE. Clinical spectrum of Li-Fraumeni syndrome/Li-Fraumeni-like syndrome in Brazilian individuals with the TP53 p.R337H mutation [Internet]. Journal of steroid biochemistry and molecular biology. 2019 ; 190 250-255.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.jsbmb.2019.04.011
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VILELA, Leticia A. P et al. KCNJ5 somatic mutation is a predictor of hypertension remission after adrenalectomy for unilateral primary aldosteronism. Journal of clinical endocrinology & metabolism, v. 104, n. 10, p. 4695-4702, 2019Tradução . . Disponível em: https://doi.org/10.1210/jc.2019-00531. Acesso em: 01 nov. 2024.
APA
Vilela, L. A. P., Rassi-cruz, M., Guimaraes, A. G., Moises, C. C. S., Freitas, T. C., Alencar, N. P., et al. (2019). KCNJ5 somatic mutation is a predictor of hypertension remission after adrenalectomy for unilateral primary aldosteronism. Journal of clinical endocrinology & metabolism, 104( 10), 4695-4702. doi:10.1210/jc.2019-00531
NLM
Vilela LAP, Rassi-cruz M, Guimaraes AG, Moises CCS, Freitas TC, Alencar NP, Zerbini MCN, Xavier ACL, Mendonça BB de, Drager LF. KCNJ5 somatic mutation is a predictor of hypertension remission after adrenalectomy for unilateral primary aldosteronism [Internet]. Journal of clinical endocrinology & metabolism. 2019 ; 104( 10): 4695-4702.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1210/jc.2019-00531
Vancouver
Vilela LAP, Rassi-cruz M, Guimaraes AG, Moises CCS, Freitas TC, Alencar NP, Zerbini MCN, Xavier ACL, Mendonça BB de, Drager LF. KCNJ5 somatic mutation is a predictor of hypertension remission after adrenalectomy for unilateral primary aldosteronism [Internet]. Journal of clinical endocrinology & metabolism. 2019 ; 104( 10): 4695-4702.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1210/jc.2019-00531
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CAVALCANTE, Isadora Pontes et al. The role of ARMC5 in human cell cultures from nodules of primary macronodular adrenocortical hyperplasia (PMAH). Molecular and cellular endocrinology, v. 460, n. C, p. 36-46, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.mce.2017.06.027. Acesso em: 01 nov. 2024.
APA
Cavalcante, I. P., Nishi, M. Y., Zerbini, M. C. N., Almeida, M. Q. de, Brondani, V. B., Botelho, M. L. A. de A., et al. (2018). The role of ARMC5 in human cell cultures from nodules of primary macronodular adrenocortical hyperplasia (PMAH). Molecular and cellular endocrinology, 460( C), 36-46. doi:10.1016/j.mce.2017.06.027
NLM
Cavalcante IP, Nishi MY, Zerbini MCN, Almeida MQ de, Brondani VB, Botelho MLA de A, Tanno FY, Srougi V, Chambo JL, Mendonça BB de, Bertherat J, Lotfi CFP, Fragoso MCB. The role of ARMC5 in human cell cultures from nodules of primary macronodular adrenocortical hyperplasia (PMAH) [Internet]. Molecular and cellular endocrinology. 2018 ; 460( C): 36-46.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.mce.2017.06.027
Vancouver
Cavalcante IP, Nishi MY, Zerbini MCN, Almeida MQ de, Brondani VB, Botelho MLA de A, Tanno FY, Srougi V, Chambo JL, Mendonça BB de, Bertherat J, Lotfi CFP, Fragoso MCB. The role of ARMC5 in human cell cultures from nodules of primary macronodular adrenocortical hyperplasia (PMAH) [Internet]. Molecular and cellular endocrinology. 2018 ; 460( C): 36-46.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.mce.2017.06.027
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERREIRA, Cristiane R et al. FOXP3-positive T-cell lymphomas in non-HTLV1 carriers include ALK-negative anaplastic large cell lymphoma: expanding the spectrum of T-cell lymphomas with regulatory phenotype. Human pathology, v. 80, p. 138-144, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.humpath.2018.06.001. Acesso em: 01 nov. 2024.
APA
Ferreira, C. R., Pereira, J., Zerbini, M. C. N., Zhao, S., Sahoo, M. K., Pinsky, B., et al. (2018). FOXP3-positive T-cell lymphomas in non-HTLV1 carriers include ALK-negative anaplastic large cell lymphoma: expanding the spectrum of T-cell lymphomas with regulatory phenotype. Human pathology, 80, 138-144. doi:10.1016/j.humpath.2018.06.001
NLM
Ferreira CR, Pereira J, Zerbini MCN, Zhao S, Sahoo MK, Pinsky B, Weber J, Lage LA de PC, Natkunam Y. FOXP3-positive T-cell lymphomas in non-HTLV1 carriers include ALK-negative anaplastic large cell lymphoma: expanding the spectrum of T-cell lymphomas with regulatory phenotype [Internet]. Human pathology. 2018 ; 80 138-144.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.humpath.2018.06.001
Vancouver
Ferreira CR, Pereira J, Zerbini MCN, Zhao S, Sahoo MK, Pinsky B, Weber J, Lage LA de PC, Natkunam Y. FOXP3-positive T-cell lymphomas in non-HTLV1 carriers include ALK-negative anaplastic large cell lymphoma: expanding the spectrum of T-cell lymphomas with regulatory phenotype [Internet]. Human pathology. 2018 ; 80 138-144.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.humpath.2018.06.001
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CAMPOS, Antonio Hugo Jose Froes Marques e ZERBINI, Maria Claudia. Frequency of EBV associated classical Hodgkin lymphoma decreases over a 54-year period in a Brazilian population. Scientific reports, v. 8, 2018Tradução . . Disponível em: https://doi.org/10.1038/s41598-018-20133-6. Acesso em: 01 nov. 2024.
APA
Campos, A. H. J. F. M., & Zerbini, M. C. (2018). Frequency of EBV associated classical Hodgkin lymphoma decreases over a 54-year period in a Brazilian population. Scientific reports, 8. doi:10.1038/s41598-018-20133-6
NLM
Campos AHJFM, Zerbini MC. Frequency of EBV associated classical Hodgkin lymphoma decreases over a 54-year period in a Brazilian population [Internet]. Scientific reports. 2018 ; 8[citado 2024 nov. 01 ] Available from: https://doi.org/10.1038/s41598-018-20133-6
Vancouver
Campos AHJFM, Zerbini MC. Frequency of EBV associated classical Hodgkin lymphoma decreases over a 54-year period in a Brazilian population [Internet]. Scientific reports. 2018 ; 8[citado 2024 nov. 01 ] Available from: https://doi.org/10.1038/s41598-018-20133-6
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MOREIRA-FILHO, Carlos Alberto et al. Minipuberty and Sexual Dimorphism in the Infant Human Thymus. Scientific reports, v. 8, 2018Tradução . . Disponível em: https://doi.org/10.1038/s41598-018-31583-3. Acesso em: 01 nov. 2024.
APA
Moreira-filho, C. A., Bando, S. Y., Bertonha, F. B., Zerbini, M. C. N., & Sampaio, M. M. S. C. (2018). Minipuberty and Sexual Dimorphism in the Infant Human Thymus. Scientific reports, 8. doi:10.1038/s41598-018-31583-3
NLM
Moreira-filho CA, Bando SY, Bertonha FB, Zerbini MCN, Sampaio MMSC. Minipuberty and Sexual Dimorphism in the Infant Human Thymus [Internet]. Scientific reports. 2018 ; 8[citado 2024 nov. 01 ] Available from: https://doi.org/10.1038/s41598-018-31583-3
Vancouver
Moreira-filho CA, Bando SY, Bertonha FB, Zerbini MCN, Sampaio MMSC. Minipuberty and Sexual Dimorphism in the Infant Human Thymus [Internet]. Scientific reports. 2018 ; 8[citado 2024 nov. 01 ] Available from: https://doi.org/10.1038/s41598-018-31583-3
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MARCHESI, Raquel et al. Morphological, immunohistochemical and cytogenetic bone marrow characterization of 12 patients with acquired aplastic anemia (AAA) that progressed to myelodysplastic syndromes (MDA). Laboratory investigation; a journal of technical methods and pathology. Baltimore: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1038/labinvest.2016.172. Acesso em: 01 nov. 2024. , 2017
APA
Marchesi, R., Velloso, E. D. R. P., Garanito, M., Siqueira, S., Azevedo Neto, R. S. de, Kumeda, C., & Zerbini, M. C. N. (2017). Morphological, immunohistochemical and cytogenetic bone marrow characterization of 12 patients with acquired aplastic anemia (AAA) that progressed to myelodysplastic syndromes (MDA). Laboratory investigation; a journal of technical methods and pathology. Baltimore: Faculdade de Medicina, Universidade de São Paulo. doi:10.1038/labinvest.2016.172
NLM
Marchesi R, Velloso EDRP, Garanito M, Siqueira S, Azevedo Neto RS de, Kumeda C, Zerbini MCN. Morphological, immunohistochemical and cytogenetic bone marrow characterization of 12 patients with acquired aplastic anemia (AAA) that progressed to myelodysplastic syndromes (MDA) [Internet]. Laboratory investigation; a journal of technical methods and pathology. 2017 ; 362A.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1038/labinvest.2016.172
Vancouver
Marchesi R, Velloso EDRP, Garanito M, Siqueira S, Azevedo Neto RS de, Kumeda C, Zerbini MCN. Morphological, immunohistochemical and cytogenetic bone marrow characterization of 12 patients with acquired aplastic anemia (AAA) that progressed to myelodysplastic syndromes (MDA) [Internet]. Laboratory investigation; a journal of technical methods and pathology. 2017 ; 362A.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1038/labinvest.2016.172
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MARCHESI, Raquel et al. Morphological, Immunohistochemical and Cytogenetic Bone Marrow Characterization of 12 Patients with Acquired Aplastic Anemia (AAA) That Progressed to Myelodysplastic Syndromes (MDS). Modern Pathology. Baltimore: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1038/modpathol.2016.253. Acesso em: 01 nov. 2024. , 2017
APA
Marchesi, R., Velloso, E., Garanito, M., Siqueira, S., Azevedo Neto, R., Kumeda, C., & Zerbini, M. C. (2017). Morphological, Immunohistochemical and Cytogenetic Bone Marrow Characterization of 12 Patients with Acquired Aplastic Anemia (AAA) That Progressed to Myelodysplastic Syndromes (MDS). Modern Pathology. Baltimore: Faculdade de Medicina, Universidade de São Paulo. doi:10.1038/modpathol.2016.253
NLM
Marchesi R, Velloso E, Garanito M, Siqueira S, Azevedo Neto R, Kumeda C, Zerbini MC. Morphological, Immunohistochemical and Cytogenetic Bone Marrow Characterization of 12 Patients with Acquired Aplastic Anemia (AAA) That Progressed to Myelodysplastic Syndromes (MDS) [Internet]. Modern Pathology. 2017 ; 30 362A.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1038/modpathol.2016.253
Vancouver
Marchesi R, Velloso E, Garanito M, Siqueira S, Azevedo Neto R, Kumeda C, Zerbini MC. Morphological, Immunohistochemical and Cytogenetic Bone Marrow Characterization of 12 Patients with Acquired Aplastic Anemia (AAA) That Progressed to Myelodysplastic Syndromes (MDS) [Internet]. Modern Pathology. 2017 ; 30 362A.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1038/modpathol.2016.253
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SERAFINI, Suellen et al. Is hematoxylin-eosin staining in rectal mucosal and submucosal biopsies still useful for the diagnosis of Hirschsprung disease?. Diagnostic pathology, v. 12, 2017Tradução . . Disponível em: https://doi.org/10.1186/s13000-017-0673-9. Acesso em: 01 nov. 2024.
APA
Serafini, S., Santos, M. M., Tannuri, A. C. A., Zerbini, M. C. N., Coelho, M. C. de M., Gonçalves, J. de O., & Tannuri, U. (2017). Is hematoxylin-eosin staining in rectal mucosal and submucosal biopsies still useful for the diagnosis of Hirschsprung disease? Diagnostic pathology, 12. doi:10.1186/s13000-017-0673-9
NLM
Serafini S, Santos MM, Tannuri ACA, Zerbini MCN, Coelho MC de M, Gonçalves J de O, Tannuri U. Is hematoxylin-eosin staining in rectal mucosal and submucosal biopsies still useful for the diagnosis of Hirschsprung disease? [Internet]. Diagnostic pathology. 2017 ; 12[citado 2024 nov. 01 ] Available from: https://doi.org/10.1186/s13000-017-0673-9
Vancouver
Serafini S, Santos MM, Tannuri ACA, Zerbini MCN, Coelho MC de M, Gonçalves J de O, Tannuri U. Is hematoxylin-eosin staining in rectal mucosal and submucosal biopsies still useful for the diagnosis of Hirschsprung disease? [Internet]. Diagnostic pathology. 2017 ; 12[citado 2024 nov. 01 ] Available from: https://doi.org/10.1186/s13000-017-0673-9
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PINHEIRO, Céline et al. GLUT1 expression in pediatric adrenocortical tumors: a promising candidate to predict clinical behavior. Oncotarget, v. 8, n. 38, p. 63835-63845, 2017Tradução . . Disponível em: https://doi.org/10.18632/oncotarget.19135. Acesso em: 01 nov. 2024.
APA
Pinheiro, C., Granja, S., Longatto-Filho, A., Faria, A. M., Fragoso, M. C. B. V., Lovisolo, S. M., et al. (2017). GLUT1 expression in pediatric adrenocortical tumors: a promising candidate to predict clinical behavior. Oncotarget, 8( 38), 63835-63845. doi:10.18632/oncotarget.19135
NLM
Pinheiro C, Granja S, Longatto-Filho A, Faria AM, Fragoso MCBV, Lovisolo SM, Bonatelli M, Costa RFA, Lerário AM, Almeida MQ, Baltazar F, Zerbini MCN. GLUT1 expression in pediatric adrenocortical tumors: a promising candidate to predict clinical behavior [Internet]. Oncotarget. 2017 ; 8( 38): 63835-63845.[citado 2024 nov. 01 ] Available from: https://doi.org/10.18632/oncotarget.19135
Vancouver
Pinheiro C, Granja S, Longatto-Filho A, Faria AM, Fragoso MCBV, Lovisolo SM, Bonatelli M, Costa RFA, Lerário AM, Almeida MQ, Baltazar F, Zerbini MCN. GLUT1 expression in pediatric adrenocortical tumors: a promising candidate to predict clinical behavior [Internet]. Oncotarget. 2017 ; 8( 38): 63835-63845.[citado 2024 nov. 01 ] Available from: https://doi.org/10.18632/oncotarget.19135
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CHANG, Claudia Veiga et al. Differential Expression of Stem Cell Markers in Human Adamantinomatous Craniopharyngioma and Pituitary Adenoma. Neuroendocrinology, v. 104, p. 183-193, 2017Tradução . . Disponível em: https://doi.org/10.1159/000446072. Acesso em: 01 nov. 2024.
APA
Chang, C. V., Araujo, R. V., Cirqueira, C. S., Cani, C. M. G., Matushita, H., Cescato, V. A. S., et al. (2017). Differential Expression of Stem Cell Markers in Human Adamantinomatous Craniopharyngioma and Pituitary Adenoma. Neuroendocrinology, 104, 183-193. doi:10.1159/000446072
NLM
Chang CV, Araujo RV, Cirqueira CS, Cani CMG, Matushita H, Cescato VAS, Fragoso MCBV, Bronstein MD, Zerbini MCN, Mendonca BB, Carvalho LR. Differential Expression of Stem Cell Markers in Human Adamantinomatous Craniopharyngioma and Pituitary Adenoma [Internet]. Neuroendocrinology. 2017 ; 104 183-193.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1159/000446072
Vancouver
Chang CV, Araujo RV, Cirqueira CS, Cani CMG, Matushita H, Cescato VAS, Fragoso MCBV, Bronstein MD, Zerbini MCN, Mendonca BB, Carvalho LR. Differential Expression of Stem Cell Markers in Human Adamantinomatous Craniopharyngioma and Pituitary Adenoma [Internet]. Neuroendocrinology. 2017 ; 104 183-193.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1159/000446072
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MARCHESI, Raquel et al. High proliferative index in acquired aplastic anemia (AAA) bone marrow does not predict progression to myelodusplastic syndromes (MDS). Laboratory investigation; a journal of technical methods and pathology. Baltimore: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1038/labinvest.2016.172. Acesso em: 01 nov. 2024. , 2017
APA
Marchesi, R., Velloso, E. D. R. P., Garanito, M., Siqueira, S., Azevedo Neto, R. S. de, Kumeda, C., & Zerbini, M. C. N. (2017). High proliferative index in acquired aplastic anemia (AAA) bone marrow does not predict progression to myelodusplastic syndromes (MDS). Laboratory investigation; a journal of technical methods and pathology. Baltimore: Faculdade de Medicina, Universidade de São Paulo. doi:10.1038/labinvest.2016.172
NLM
Marchesi R, Velloso EDRP, Garanito M, Siqueira S, Azevedo Neto RS de, Kumeda C, Zerbini MCN. High proliferative index in acquired aplastic anemia (AAA) bone marrow does not predict progression to myelodusplastic syndromes (MDS) [Internet]. Laboratory investigation; a journal of technical methods and pathology. 2017 ; 362A.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1038/labinvest.2016.172
Vancouver
Marchesi R, Velloso EDRP, Garanito M, Siqueira S, Azevedo Neto RS de, Kumeda C, Zerbini MCN. High proliferative index in acquired aplastic anemia (AAA) bone marrow does not predict progression to myelodusplastic syndromes (MDS) [Internet]. Laboratory investigation; a journal of technical methods and pathology. 2017 ; 362A.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1038/labinvest.2016.172
