Detalhe da pesquisa
1.
Genomic and transcriptomic correlates of Richter transformation in chronic lymphocytic leukemia.
Blood
; 137(20): 2800-2816, 2021 05 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-33206936
2.
Complement activation negatively affects the platelet response to thrombopoietin receptor agonists in patients with immune thrombocytopenia: a prospective cohort study.
Platelets
; 34(1): 2159019, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-36636835
3.
Bone mineral density in haemophilia - a multicentre study evaluating the impact of different replacement regimens.
Haemophilia
; 28(2): 239-246, 2022 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-34994489
4.
Biomarkers of Complement and Platelet Activation are not correlated with the One or Twenty-Four Hours Corrected Count Increments in Prophylactically Platelet Transfused Hematological Patients: a Prospective Cohort Study.
Platelets
; 33(3): 350-359, 2022 Apr 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34210243
5.
First-line therapy in chronic lymphocytic leukemia: a Swedish nation-wide real-world study on 1053 consecutive patients treated between 2007 and 2013.
Haematologica
; 104(4): 797-804, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30467205
6.
Clinical-grade validation of whole genome sequencing reveals robust detection of low-frequency variants and copy number alterations in CLL.
Br J Haematol
; 182(3): 412-417, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29808933
7.
Application of whole-exome sequencing to direct the specific functional testing and diagnosis of rare inherited bleeding disorders in patients from the Öresund Region, Scandinavia.
Br J Haematol
; 179(2): 308-322, 2017 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-28748566
8.
Indications of underdiagnosis of atypical haemolytic uraemic syndrome in a cohort referred to the Coagulation Unit in Malmo, Sweden, for analysis of ADAMTS13 2007-2012.
Nephrology (Carlton)
; 22(7): 555-561, 2017 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-27175932
9.
Long-term anti-FVIII antibody response in Bethesda-negative haemophilia A patients receiving continuous replacement therapy.
Br J Haematol
; 163(3): 385-92, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-24032553
10.
Clinical characterization and identification of rare genetic variants in atypical hemolytic uremic syndrome: A Swedish retrospective observational study.
Ther Apher Dial
; 25(6): 988-1000, 2021 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-33609329
11.
Combination of FVIII and by-passing agent potentiates in vitro thrombin production in haemophilia A inhibitor plasma.
Br J Haematol
; 151(4): 381-6, 2010 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-20977448
12.
SAMHD1 Limits the Efficacy of Forodesine in Leukemia by Protecting Cells against the Cytotoxicity of dGTP.
Cell Rep
; 31(6): 107640, 2020 05 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32402273
13.
At the Cross Section of Thrombotic Microangiopathy and Atypical Hemolytic Uremic Syndrome: A Narrative Review of Differential Diagnostics and a Problematization of Nomenclature.
Ther Apher Dial
; 21(4): 304-319, 2017 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-28508588
14.
Quiescence of hematopoietic stem cells and maintenance of the stem cell pool is not dependent on TGF-beta signaling in vivo.
Exp Hematol
; 33(5): 592-6, 2005 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-15850837
15.
Haematopoietic stem cells retain long-term repopulating activity and multipotency in the absence of stem-cell leukaemia SCL/tal-1 gene.
Nature
; 421(6922): 547-51, 2003 Jan 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-12540851