Detalhe da pesquisa
1.
CALR-mutated patients with low allele burden represent a specific subtype of essential thrombocythemia: A study on behalf of FIM and GBMHM.
Am J Hematol
; 99(5): 1001-1004, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38404143
2.
Relationship between comorbidities, mutational profile, and outcome after intensive chemotherapy in patients older than 60 years with acute myeloid leukemia: Assessment of different risk scores.
Am J Hematol
; 98(6): 922-931, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36964937
3.
Diagnosis and prognosis are supported by integrated assessment of next-generation sequencing in chronic myeloid malignancies. A real-life study.
Haematologica
; 106(3): 701-707, 2021 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32241844
4.
Risk of infection according to the gamma globulin level in the 100 days following allogeneic stem cell transplantations.
Eur J Haematol
; 107(4): 489-496, 2021 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-34245060
5.
Targeted molecular characterization shows differences between primary and secondary myelofibrosis.
Genes Chromosomes Cancer
; 59(1): 30-39, 2020 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-31340059
6.
Sequential mutational evaluation of CALR -mutated myeloproliferative neoplasms with thrombocytosis reveals an association between CALR allele burden evolution and disease progression.
Br J Haematol
; 188(6): 935-944, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31710700
7.
WT1 gene is overexpressed in myeloproliferative neoplasms, especially in myelofibrosis.
Blood Cells Mol Dis
; 75: 35-40, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30612065
8.
Association of MPL K39N and R102P heterozygous germline mutations lead to hereditary thrombocytosis.
Am J Hematol
; 2024 May 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-38752375
9.
Presence of atypical thrombopoietin receptor (MPL) mutations in triple-negative essential thrombocythemia patients.
Blood
; 127(3): 333-42, 2016 Jan 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-26450985
10.
Non-adherence to treatment with cytoreductive and/or antithrombotic drugs is frequent and associated with an increased risk of complications in patients with polycythemia vera or essential thrombocythemia (OUEST study).
Haematologica
; 103(4): 607-613, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29246923
11.
Benefits and pitfalls of pegylated interferon-α2a therapy in patients with myeloproliferative neoplasm-associated myelofibrosis: a French Intergroup of Myeloproliferative neoplasms (FIM) study.
Haematologica
; 103(3): 438-446, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29217781
12.
Donor cell-derived acute promyelocytic leukemia after allogeneic hematopoietic stem cell transplantation.
Eur J Haematol
; 101(4): 570-574, 2018 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-30007088
13.
Comparison of four methods to assess high-on platelet reactivity under P2Y12 receptor inhibitor.
Platelets
; 29(3): 257-264, 2018 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-29580115
14.
Sequential analysis of 18 genes in polycythemia vera and essential thrombocythemia reveals an association between mutational status and clinical outcome.
Genes Chromosomes Cancer
; 56(5): 354-362, 2017 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-27997717
15.
Clinical and molecular response to interferon-α therapy in essential thrombocythemia patients with CALR mutations.
Blood
; 126(24): 2585-91, 2015 Dec 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-26486786
16.
Histological and genetic characterization and follow-up of 130 patients with chronic triple-negative thrombocytosis.
Haematologica
; 107(11): 2725-2731, 2022 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35833299
17.
Acute myeloid leukaemia (FAB AML-M4Eo) with cryptic insertion of cbfb resulting in cbfb-Myh11 fusion.
Hematol Oncol
; 35(3): 385-389, 2017 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-28906004
18.
JAK2V617F and calreticulin mutations in recurrent venous thromboembolism: results from the EDITH prospective cohort.
Ann Hematol
; 96(3): 383-386, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-27766390
19.
Different number of circulating CD34 + cells in essential thrombocythemia, prefibrotic/early primary myelofibrosis, and overt primary myelofibrosis.
Ann Hematol
; 101(4): 893-896, 2022 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-34611719
20.
No detection of atypical one-base deletion of CALR exon 9 with fragment analysis: A molecular trap to avoid.
Blood Cells Mol Dis
; 90: 102589, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34214802