Detalhe da pesquisa
1.
Ubiquitination of hnRNPA1 by TRAF6 links chronic innate immune signaling with myelodysplasia.
Nat Immunol;
18(2): 236-245, 2017 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28024152
2.
Oral Iptacopan Monotherapy in Paroxysmal Nocturnal Hemoglobinuria.
N Engl J Med;
390(11): 994-1008, 2024 Mar 14.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38477987
3.
Paroxysmal nocturnal hemoglobinuria-related thrombosis in the era of novel therapies: a 2043 patient/years analysis.
Blood;
2024 Mar 21.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38513233
4.
Impact of TP53 on outcome of patients with myelofibrosis undergoing hematopoietic stem cell transplantation.
Blood;
141(23): 2901-2911, 2023 06 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36940410
5.
Germ line DDX41 mutations define a unique subtype of myeloid neoplasms.
Blood;
141(5): 534-549, 2023 02 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36322930
6.
Splenectomy outcomes in immune cytopenias: Treatment outcomes and determinants of response.
J Intern Med;
295(2): 229-241, 2024 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37953670
7.
Corrigendum: Ubiquitination of hnRNPA1 by TRAF6 links chronic innate immune signaling with myelodysplasia.
Nat Immunol;
18(4): 474, 2017 03 22.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28323261
8.
Splenic irradiation for myelofibrosis prior to hematopoietic cell transplantation: A global collaborative analysis.
Am J Hematol;
99(5): 844-853, 2024 May.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38357714
9.
The clinicopathologic significance of NPM1 mutation and ability to detect mutated NPM1 by immunohistochemistry in non-AML myeloid neoplasms.
Genes Chromosomes Cancer;
62(10): 573-580, 2023 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36959701
10.
How I manage acquired pure red cell aplasia in adults.
Blood;
137(15): 2001-2009, 2021 04 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33657207
11.
Phase 2 study of danicopan in patients with paroxysmal nocturnal hemoglobinuria with an inadequate response to eculizumab.
Blood;
138(20): 1928-1938, 2021 11 18.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34314483
12.
The similarity of class II HLA genotypes defines patterns of autoreactivity in idiopathic bone marrow failure disorders.
Blood;
138(26): 2781-2798, 2021 12 30.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34748628
13.
Machine learning integrates genomic signatures for subclassification beyond primary and secondary acute myeloid leukemia.
Blood;
138(19): 1885-1895, 2021 11 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34075412
14.
Relationship of paroxysmal nocturnal hemoglobinuria (PNH) granulocyte clone size to disease burden and risk of major vascular events in untreated patients: results from the International PNH Registry.
Ann Hematol;
102(7): 1637-1644, 2023 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37199789
15.
Concomitant Immunosuppressive Therapy and Eculizumab Use in Patients with Paroxysmal Nocturnal Hemoglobinuria: An International PNH Registry Analysis.
Acta Haematol;
146(1): 1-13, 2023.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36108594
16.
Machine learning demonstrates that somatic mutations imprint invariant morphologic features in myelodysplastic syndromes.
Blood;
136(20): 2249-2262, 2020 11 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32961553
17.
HHEX promotes myeloid transformation in cooperation with mutant ASXL1.
Blood;
136(14): 1670-1684, 2020 10 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32492700
18.
Molecular landscape and clonal architecture of adult myelodysplastic/myeloproliferative neoplasms.
Blood;
136(16): 1851-1862, 2020 10 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32573691
19.
SF3B1-mutant MDS as a distinct disease subtype: a proposal from the International Working Group for the Prognosis of MDS.
Blood;
136(2): 157-170, 2020 07 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32347921
20.
A study of Telomerase Reverse Transcriptase rare variants in myeloid neoplasia.
Hematol Oncol;
40(4): 812-817, 2022 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35106810