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Artigo de periodico-carta/editorial
IPSS-M in myelodysplastic neoplasms arising from aplastic anemia and paroxysmal nocturnal hemoglobinuria [Carta] (2023)
Gurnari, Carmelo; Prata, Pedro Henrique de Lima; Catto, Luiz Fernando Bazzo ; Durmaz, Arda; Pinto, André Luiz; Inacio, Mariana Carolina Beraldo; Hernandez, Lucie; Dhedin, Nathalie; Visconte, Valeria; Soulier, Jean; Calado, Rodrigo Tocantins
Fonte: Blood. Unidade: FMRP
Assuntos: ANEMIA, NEOPLASIAS, DOENÇAS RARAS, LEUCEMIA MIELOIDE AGUDA
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ABNT
GURNARI, Carmelo et al. IPSS-M in myelodysplastic neoplasms arising from aplastic anemia and paroxysmal nocturnal hemoglobinuria [Carta]. Blood. Washington: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://doi.org/10.1182/blood.2023020108. Acesso em: 23 out. 2025. , 2023
APA
Gurnari, C., Prata, P. H. de L., Catto, L. F. B., Durmaz, A., Pinto, A. L., Inacio, M. C. B., et al. (2023). IPSS-M in myelodysplastic neoplasms arising from aplastic anemia and paroxysmal nocturnal hemoglobinuria [Carta]. Blood. Washington: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. doi:10.1182/blood.2023020108
NLM
Gurnari C, Prata PH de L, Catto LFB, Durmaz A, Pinto AL, Inacio MCB, Hernandez L, Dhedin N, Visconte V, Soulier J, Calado RT. IPSS-M in myelodysplastic neoplasms arising from aplastic anemia and paroxysmal nocturnal hemoglobinuria [Carta] [Internet]. Blood. 2023 ; 141( 25): 3122-3125.[citado 2025 out. 23 ] Available from: https://doi.org/10.1182/blood.2023020108
Vancouver
Gurnari C, Prata PH de L, Catto LFB, Durmaz A, Pinto AL, Inacio MCB, Hernandez L, Dhedin N, Visconte V, Soulier J, Calado RT. IPSS-M in myelodysplastic neoplasms arising from aplastic anemia and paroxysmal nocturnal hemoglobinuria [Carta] [Internet]. Blood. 2023 ; 141( 25): 3122-3125.[citado 2025 out. 23 ] Available from: https://doi.org/10.1182/blood.2023020108
Trabalho de evento-resumo periodico
Molecular international prognostic Scoring System (IPSS-M) in myelodysplastic syndromes arising from aplastic anemia and paroxysmal nocturnal hemoglobinuria (2022)
Gurnari, Carmelo; Prata, Pedro H.; Catto, Luiz Fernando Bazzo ; Durmaz, Arda; Larcher, Lise; Sebert, Marie; Allain, Vincent; Kewan, Tariq; Pagliuca, Simona; Pinto, André Luiz; Inacio, Mariana Carolina Beraldo; Hernandez, Lucie; Dhedin, Nathalie; Caillat-Zucman, Sophie; Clappier, Emmanuelle; Fontbrune, Flore Sicre de; Voso, Maria Teresa; Visconte, Valeria; Peffault de Latour, Regis; Soulier, Jean; Socie, Gerard; Calado, Rodrigo Tocantins ; Maciejewski, Jaroslaw P.
Fonte: Blood. Nome do evento: ASH Annual Meeting and Exposition. Unidade: FMRP
Assuntos: ANEMIA, LEUCEMIA MIELOIDE, CITOGENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GURNARI, Carmelo et al. Molecular international prognostic Scoring System (IPSS-M) in myelodysplastic syndromes arising from aplastic anemia and paroxysmal nocturnal hemoglobinuria. Blood. Amsterdam: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://doi.org/10.1182/blood-2022-160458. Acesso em: 23 out. 2025. , 2022
APA
Gurnari, C., Prata, P. H., Catto, L. F. B., Durmaz, A., Larcher, L., Sebert, M., et al. (2022). Molecular international prognostic Scoring System (IPSS-M) in myelodysplastic syndromes arising from aplastic anemia and paroxysmal nocturnal hemoglobinuria. Blood. Amsterdam: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. doi:10.1182/blood-2022-160458
NLM
Gurnari C, Prata PH, Catto LFB, Durmaz A, Larcher L, Sebert M, Allain V, Kewan T, Pagliuca S, Pinto AL, Inacio MCB, Hernandez L, Dhedin N, Caillat-Zucman S, Clappier E, Fontbrune FS de, Voso MT, Visconte V, Peffault de Latour R, Soulier J, Socie G, Calado RT, Maciejewski JP. Molecular international prognostic Scoring System (IPSS-M) in myelodysplastic syndromes arising from aplastic anemia and paroxysmal nocturnal hemoglobinuria [Internet]. Blood. 2022 ; 140( suppl. 1): 5788-5789.[citado 2025 out. 23 ] Available from: https://doi.org/10.1182/blood-2022-160458
Vancouver
Gurnari C, Prata PH, Catto LFB, Durmaz A, Larcher L, Sebert M, Allain V, Kewan T, Pagliuca S, Pinto AL, Inacio MCB, Hernandez L, Dhedin N, Caillat-Zucman S, Clappier E, Fontbrune FS de, Voso MT, Visconte V, Peffault de Latour R, Soulier J, Socie G, Calado RT, Maciejewski JP. Molecular international prognostic Scoring System (IPSS-M) in myelodysplastic syndromes arising from aplastic anemia and paroxysmal nocturnal hemoglobinuria [Internet]. Blood. 2022 ; 140( suppl. 1): 5788-5789.[citado 2025 out. 23 ] Available from: https://doi.org/10.1182/blood-2022-160458
Trabalho de evento-resumo periodico
Immunogenetic, molecular and clinical determinants of clonal evolution in aplastic anemia and paroxysmal nocturnal hemoglobinuria (2021)
Gurnari, Carmelo; Pagliuca, Simona; Prata, Pedro Henrique de Lima; Catto, Luiz Fernando Bazzo ; Larcher, Lise; Sebert, Marie; Allain, Vincent; Patel, Bhumika J.; Terkawi, Laila; Santos, André Luiz Pinto ; Inacio, Mariana Carolina Beraldo; Hernandez, Lucie; Dhedin, Nathalie; Caillat-Zucman, Sophie; Clappier, Emmanuelle; Fontbrune, Flore Sicre de; Voso, Maria Teresa; Visconte, Valeria; Socie, Gerard; Calado, Rodrigo Tocantins ; Peffault de Latour, Regis; Soulier, Jean; Maciejewski, Jaroslaw P.
Fonte: Blood. Nome do evento: ASH Annual Meeting Abstracts. Unidade: FMRP
Assuntos: ANEMIA, CONTAGEM DE CÉLULAS SANGUÍNEAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GURNARI, Carmelo et al. Immunogenetic, molecular and clinical determinants of clonal evolution in aplastic anemia and paroxysmal nocturnal hemoglobinuria. Blood. Washington: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://doi.org/10.1182/blood-2021-147556. Acesso em: 23 out. 2025. , 2021
APA
Gurnari, C., Pagliuca, S., Prata, P. H. de L., Catto, L. F. B., Larcher, L., Sebert, M., et al. (2021). Immunogenetic, molecular and clinical determinants of clonal evolution in aplastic anemia and paroxysmal nocturnal hemoglobinuria. Blood. Washington: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. doi:10.1182/blood-2021-147556
NLM
Gurnari C, Pagliuca S, Prata PH de L, Catto LFB, Larcher L, Sebert M, Allain V, Patel BJ, Terkawi L, Santos ALP, Inacio MCB, Hernandez L, Dhedin N, Caillat-Zucman S, Clappier E, Fontbrune FS de, Voso MT, Visconte V, Socie G, Calado RT, Peffault de Latour R, Soulier J, Maciejewski JP. Immunogenetic, molecular and clinical determinants of clonal evolution in aplastic anemia and paroxysmal nocturnal hemoglobinuria [Internet]. Blood. 2021 ; 138 602-602.[citado 2025 out. 23 ] Available from: https://doi.org/10.1182/blood-2021-147556
Vancouver
Gurnari C, Pagliuca S, Prata PH de L, Catto LFB, Larcher L, Sebert M, Allain V, Patel BJ, Terkawi L, Santos ALP, Inacio MCB, Hernandez L, Dhedin N, Caillat-Zucman S, Clappier E, Fontbrune FS de, Voso MT, Visconte V, Socie G, Calado RT, Peffault de Latour R, Soulier J, Maciejewski JP. Immunogenetic, molecular and clinical determinants of clonal evolution in aplastic anemia and paroxysmal nocturnal hemoglobinuria [Internet]. Blood. 2021 ; 138 602-602.[citado 2025 out. 23 ] Available from: https://doi.org/10.1182/blood-2021-147556
Artigo de periodico-carta/editorial
SF3B1 mutations are infrequently found in non-myelodysplastic bone marrow failure syndromes and mast cell diseases but, if present, are associated with the ring sideroblast phenotype (2013)
Visconte, Valeria; Tabarroki, Ali; Rogers, Heesun J.; Hasrouni, Edy; Traina, Fabiola; Makishima, Hideki; Hamilton, Betty K.; Liu, Yang; O'Keefe, Christine; Lichtin, Alan; Horwitz, Leonard; Sekeres, Mikkael A.; Hsieh, Fred H.; Tiu, Ramon V.
Fonte: Haematologica. Unidade: FMRP
Assuntos: HEMATOLOGIA, CÉLULAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VISCONTE, Valeria et al. SF3B1 mutations are infrequently found in non-myelodysplastic bone marrow failure syndromes and mast cell diseases but, if present, are associated with the ring sideroblast phenotype. Haematologica. Pavia: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://doi.org/10.3324/haematol.2013.090506. Acesso em: 23 out. 2025. , 2013
APA
Visconte, V., Tabarroki, A., Rogers, H. J., Hasrouni, E., Traina, F., Makishima, H., et al. (2013). SF3B1 mutations are infrequently found in non-myelodysplastic bone marrow failure syndromes and mast cell diseases but, if present, are associated with the ring sideroblast phenotype. Haematologica. Pavia: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. doi:10.3324/haematol.2013.090506
NLM
Visconte V, Tabarroki A, Rogers HJ, Hasrouni E, Traina F, Makishima H, Hamilton BK, Liu Y, O'Keefe C, Lichtin A, Horwitz L, Sekeres MA, Hsieh FH, Tiu RV. SF3B1 mutations are infrequently found in non-myelodysplastic bone marrow failure syndromes and mast cell diseases but, if present, are associated with the ring sideroblast phenotype [Internet]. Haematologica. 2013 ; 98( 9): e105-e107.[citado 2025 out. 23 ] Available from: https://doi.org/10.3324/haematol.2013.090506
Vancouver
Visconte V, Tabarroki A, Rogers HJ, Hasrouni E, Traina F, Makishima H, Hamilton BK, Liu Y, O'Keefe C, Lichtin A, Horwitz L, Sekeres MA, Hsieh FH, Tiu RV. SF3B1 mutations are infrequently found in non-myelodysplastic bone marrow failure syndromes and mast cell diseases but, if present, are associated with the ring sideroblast phenotype [Internet]. Haematologica. 2013 ; 98( 9): e105-e107.[citado 2025 out. 23 ] Available from: https://doi.org/10.3324/haematol.2013.090506

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