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1
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
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
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Artigo 		Adicionar ao Meu Espaço

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

Valeria Visconte Ali Tabarroki; Heesun J Rogers; Edy Hasrouni; Fabiola Traina; Hideki Makishima; Betty K Hamilton; Yang Liu; Christine O'Keefe; Alan Lichtin; Leonard Horwitz; Mikkael A Sekeres; Fred H Hsieh; Ramon V Tiu

Haematologica Pavia v. 98, n. 9, p. e105-e107, 2013

Pavia 2013

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2450177 Estantes Deslizantes )(Acessar)

2
IPSS-M in myelodysplastic neoplasms arising from aplastic anemia and paroxysmal nocturnal hemoglobinuria [Carta]
IPSS-M in myelodysplastic neoplasms arising from aplastic anemia and paroxysmal nocturnal hemoglobinuria [Carta]
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IPSS-M in myelodysplastic neoplasms arising from aplastic anemia and paroxysmal nocturnal hemoglobinuria [Carta]

Carmelo Gurnari Pedro Henrique de Lima Prata; Luiz Fernando Bazzo Catto; Arda Durmaz; André Luiz Pinto; Mariana Carolina Beraldo Inacio; Lucie Hernandez; Nathalie Dhedin; Valeria Visconte; Jean Soulier; Rodrigo Tocantins Calado

Blood Washington v. 141, n. 25, p. 3122-3125, 2023

Washington 2023

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 3192084 Acervo Digital )(Acessar)

3
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
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
Material Type:
Artigo 		Adicionar ao Meu Espaço

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

Valeria Visconte Ali Tabarroki; Heesun J Rogers; Edy Hasrouni; Fabiola Traina; Hideki Makishima; Betty K Hamilton; Yang Liu; Christine O'Keefe; Alan Lichtin; Leonard Horwitz; Mikkael A Sekeres; Fred H Hsieh; Ramon V Tiu

Haematologica Pavia v. 98, n. 9, p. e105-e107, 2013

Pavia 2013

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2450177 Estantes Deslizantes )(Acessar)

4
Familial systemic mastocytosis with germline KIT K509I mutation is sensitive to treatment with imatinib, dasatinib and PKC412
Familial systemic mastocytosis with germline KIT K509I mutation is sensitive to treatment with imatinib, dasatinib and PKC412
Material Type:
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Familial systemic mastocytosis with germline KIT K509I mutation is sensitive to treatment with imatinib, dasatinib and PKC412

Paula de Melo Campos João Agostinho Machado Neto; Renata Scopim-Ribeiro; Valeria Visconte; Ali Tabarroki; Adriana S. S Duarte; Flávia F. C Barra; José Vassalo; Heesun J Rogers; Irene Lorand-Metze; Ramon V Tiu; Fernando F Costa; Sara T. Olalla Saad; Fabiola Traina

Leukemia Research Kidlington v. 38, n. 10, p. 1245-1251, 2014

Kidlington 2014

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2707111 Estantes Deslizantes )(Acessar)

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  1. Haematologica  (2)
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Deste Autor:

  1. Visconte, V
  2. Traina, F
  3. Tiu, R
  4. Tabarroki, A
  5. Rogers, H

Neste Assunto:

  1. Hematologia
  2. Células
  3. Apoptose (Efeitos De Drogas)
  4. Neoplasias
  5. Doenças Raras

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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