Works matching IS 00071048 AND DT 2022 AND VI 198 AND IP 4
Results: 29
Splicing factor 3B subunit 1 (SF3B1) mutation in the context of therapy‐related myelodysplastic syndromes.
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- British Journal of Haematology, 2022, v. 198, n. 4, p. 713, doi. 10.1111/bjh.18319
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New biomarker paves the way for a clinical trial for neurodegeneration in Langerhans cell histiocytosis.
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- British Journal of Haematology, 2022, v. 198, n. 4, p. 623, doi. 10.1111/bjh.18308
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Ibrutinib use, treatment duration, and concomitant medications in Australian patients with relapsed or refractory chronic lymphocytic leukaemia.
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- British Journal of Haematology, 2022, v. 198, n. 4, p. 790, doi. 10.1111/bjh.18306
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Cytoreductive treatment and association with platelet function and maturity in patients with essential thrombocythaemia.
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- British Journal of Haematology, 2022, v. 198, n. 4, p. 693, doi. 10.1111/bjh.18303
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A biomarker signature to predict complete response to itacitinib and corticosteroids in acute graft‐versus‐host disease.
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- British Journal of Haematology, 2022, v. 198, n. 4, p. 729, doi. 10.1111/bjh.18300
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Skin manifestations of intravascular adult T‐cell leukaemia/lymphoma.
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- British Journal of Haematology, 2022, v. 198, n. 4, p. 618, doi. 10.1111/bjh.18318
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Optimizing haematopoietic stem and progenitor cell apheresis collection from plerixafor‐mobilized patients with sickle cell disease.
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- British Journal of Haematology, 2022, v. 198, n. 4, p. 740, doi. 10.1111/bjh.18311
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Heavy chain/light chain assay is a useful biomarker for diagnosis and management of patients with cold agglutinin disease.
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- British Journal of Haematology, 2022, v. 198, n. 4, p. e67, doi. 10.1111/bjh.18317
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The clinical influence of preformed nonspecific anti‐HLA antibodies on single‐unit umbilical cord blood transplantation in patients with haematological malignancies.
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- British Journal of Haematology, 2022, v. 198, n. 4, p. e63, doi. 10.1111/bjh.18316
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Reduction in seroprevalence of viral transfusion‐transmitted infections in southwest Nigeria in children with sickle cell disease using an enhanced screening strategy.
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- British Journal of Haematology, 2022, v. 198, n. 4, p. 745, doi. 10.1111/bjh.18313
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Impaired humoral and cellular response to primary COVID‐19 vaccination in patients less than 2 years after allogeneic bone marrow transplant.
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- British Journal of Haematology, 2022, v. 198, n. 4, p. 668, doi. 10.1111/bjh.18312
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The impact of COVID‐19 on related‐donor allogeneic stem cell harvest processes: A British Society of Blood and Marrow Transplantation and Cellular Therapy survey.
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- British Journal of Haematology, 2022, v. 198, n. 4, p. e51, doi. 10.1111/bjh.18299
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Outcomes of allogeneic haematopoietic cell transplantation for chronic neutrophilic leukaemia: A combined CIBMTR/CMWP of EBMT analysis.
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- British Journal of Haematology, 2022, v. 198, n. 4, p. 785, doi. 10.1111/bjh.18297
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Anti‐SARS‐CoV‐19 antibodies in children and adults with sickle cell disease: A single‐site analysis in New York City.
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- British Journal of Haematology, 2022, v. 198, n. 4, p. 680, doi. 10.1111/bjh.18294
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Empagliflozin modulates CD4<sup>+</sup> T‐cell differentiation via metabolic reprogramming in immune thrombocytopenia.
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- British Journal of Haematology, 2022, v. 198, n. 4, p. 765, doi. 10.1111/bjh.18293
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Menstrual problems in chronic immune thrombocytopenia: A monthly challenge ‐ a cohort study and review.
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- British Journal of Haematology, 2022, v. 198, n. 4, p. 753, doi. 10.1111/bjh.18291
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Isocitrate dehydrogenase inhibitors as a bridge to allogeneic stem cell transplant in relapsed or refractory acute myeloid leukaemia.
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- British Journal of Haematology, 2022, v. 198, n. 4, p. 780, doi. 10.1111/bjh.18290
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Sustained sutimlimab response for 3 years in patients with cold agglutinin disease: A phase I, open‐label, extension trial.
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- British Journal of Haematology, 2022, v. 198, n. 4, p. e59, doi. 10.1111/bjh.18289
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Limited activity of fedratinib in myelofibrosis patients relapsed/refractory to ruxolitinib 20 mg twice daily or higher: A real‐world experience.
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- British Journal of Haematology, 2022, v. 198, n. 4, p. e54, doi. 10.1111/bjh.18284
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Favourable outcomes of double‐hit/double‐expressor lymphoma and high‐grade B‐cell lymphoma, not otherwise specified after early dose‐intensive treatment and up‐front autologous stem cell transplantation: a single‐centre retrospective experience
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- British Journal of Haematology, 2022, v. 198, n. 4, p. 776, doi. 10.1111/bjh.18280
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Haematological management of major haemorrhage: a British Society for Haematology Guideline.
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- British Journal of Haematology, 2022, v. 198, n. 4, p. 654, doi. 10.1111/bjh.18275
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Clinical implications and genetic features of clonal cytopenia of undetermined significance compared to lower‐risk myelodysplastic syndrome.
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- British Journal of Haematology, 2022, v. 198, n. 4, p. 703, doi. 10.1111/bjh.18273
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Screening for neurodegeneration in Langerhans cell histiocytosis with neurofilament light in plasma.
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- British Journal of Haematology, 2022, v. 198, n. 4, p. 721, doi. 10.1111/bjh.18247
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Major haemorrhage: putting evidence into practice.
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- British Journal of Haematology, 2022, v. 198, n. 4, p. 619, doi. 10.1111/bjh.18246
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Pure erythroid leukaemia mimicking metastatic carcinoma.
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- British Journal of Haematology, 2022, v. 198, n. 4, p. 617, doi. 10.1111/bjh.18244
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Outcomes of Hodgkin variant Richter transformation in chronic lymphocytic leukaemia and small lymphocytic lymphoma in British Columbia.
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- British Journal of Haematology, 2022, v. 198, n. 4, p. 684, doi. 10.1111/bjh.18241
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The potential role of mass spectrometry for the identification and monitoring of patients with plasma cell disorders: Where are we now and which questions remain unanswered?
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- British Journal of Haematology, 2022, v. 198, n. 4, p. 641, doi. 10.1111/bjh.18226
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The significance of mixed chimaerism and cell lineage chimaerism monitoring in paediatric patients post haematopoietic stem cell transplant.
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- British Journal of Haematology, 2022, v. 198, n. 4, p. 625, doi. 10.1111/bjh.18190
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Issue Information.
- Published in:
- British Journal of Haematology, 2022, v. 198, n. 4, p. 613, doi. 10.1111/bjh.17598
- Publication type:
- Article