Works matching IS 00071048 AND DT 2023 AND VI 202 AND IP 5
Results: 30
FISH‐ing for answers: Can genomic arrays add to our understanding of disease biology in low‐risk chronic lymphocytic leukaemia?
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- British Journal of Haematology, 2023, v. 202, n. 5, p. 922, doi. 10.1111/bjh.18992
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Early treatment for COVID‐19 in patients with haematological malignancies: Much more than a recommendation!
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- British Journal of Haematology, 2023, v. 202, n. 5, p. 913, doi. 10.1111/bjh.18977
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Metformin sensitizes AML cells to venetoclax through endoplasmic reticulum stress—CHOP pathway.
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- British Journal of Haematology, 2023, v. 202, n. 5, p. 971, doi. 10.1111/bjh.18968
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A novel gain‐of‐function PIP4K2A mutation elevates the expression of β‐globin and aggravates the severity of α‐thalassemia.
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- British Journal of Haematology, 2023, v. 202, n. 5, p. 1018, doi. 10.1111/bjh.18967
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High prevalence of persistent COVID‐19‐related health anxiety and social restriction in patients with haematological disorders.
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- British Journal of Haematology, 2023, v. 202, n. 5, p. 1065, doi. 10.1111/bjh.18960
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First use of ibrutinib for the treatment of post‐transplant central nervous system graft‐versus‐host disease.
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- British Journal of Haematology, 2023, v. 202, n. 5, p. 1061, doi. 10.1111/bjh.18959
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The (near) miracle of therapy in chronic myeloid leukaemia.
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- British Journal of Haematology, 2023, v. 202, n. 5, p. 919, doi. 10.1111/bjh.18956
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Vertebral fractures and low lean mass in young men with sickle cell disease: Lack of association with bone mineral density and clinical characteristics.
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- British Journal of Haematology, 2023, v. 202, n. 5, p. e46, doi. 10.1111/bjh.18954
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Patient‐derived xenograft models of ALK+ ALCL reveal preclinical promise for therapy with brigatinib.
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- British Journal of Haematology, 2023, v. 202, n. 5, p. 985, doi. 10.1111/bjh.18953
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Clonal architecture and single‐cell transcriptome landscape in Richter's syndrome.
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- British Journal of Haematology, 2023, v. 202, n. 5, p. 1055, doi. 10.1111/bjh.18952
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Transfusion of red cells from donors with hereditary haemochromatosis improve haemoglobin increments in patients.
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- British Journal of Haematology, 2023, v. 202, n. 5, p. 1052, doi. 10.1111/bjh.18951
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Next‐generation diagnostic instruments in haematology.
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- British Journal of Haematology, 2023, v. 202, n. 5, p. 925, doi. 10.1111/bjh.18949
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Functional and psychological impact of minimal residual disease assessment on patients with multiple myeloma.
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- British Journal of Haematology, 2023, v. 202, n. 5, p. e43, doi. 10.1111/bjh.18948
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- Article
Additional lesions identified by genomic microarrays are associated with an inferior outcome in low‐risk chronic lymphocytic leukaemia patients.
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- British Journal of Haematology, 2023, v. 202, n. 5, p. 953, doi. 10.1111/bjh.18946
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Genetic variants causing G6PD deficiency: Clinical and biochemical data support new WHO classification.
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- British Journal of Haematology, 2023, v. 202, n. 5, p. 1024, doi. 10.1111/bjh.18943
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- Article
Dose‐dependent expression of GFI1 alters metabolism in the haematopoietic progenitors and MLL::AF9‐induced leukaemic cells.
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- British Journal of Haematology, 2023, v. 202, n. 5, p. 1033, doi. 10.1111/bjh.18939
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Vaccination in sickle cell disease: Immunocompromised or immunocompetent?
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- British Journal of Haematology, 2023, v. 202, n. 5, p. 916, doi. 10.1111/bjh.18942
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- Article
Successful treatment of a chemotherapy‐resistant t(17;19) paediatric ALL with a combination of inotuzumab, venetoclax and navitoclax.
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- British Journal of Haematology, 2023, v. 202, n. 5, p. e39, doi. 10.1111/bjh.18936
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Mitochondria retention in mature RBCs from haemoglobin SC patients.
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- British Journal of Haematology, 2023, v. 202, n. 5, p. e36, doi. 10.1111/bjh.18935
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Needs assessment in adults and parents of children living with sickle cell disease in Jamaica.
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- British Journal of Haematology, 2023, v. 202, n. 5, p. e31, doi. 10.1111/bjh.18917
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A national survey assessing prevention of hospital‐associated venous thromboembolism in English Mental Health Trusts.
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- British Journal of Haematology, 2023, v. 202, n. 5, p. 1049, doi. 10.1111/bjh.18913
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Clinical decision support to reduce unnecessary diagnostic testing for heparin‐induced thrombocytopenia.
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- British Journal of Haematology, 2023, v. 202, n. 5, p. 1011, doi. 10.1111/bjh.18902
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Enhanced IgG immune response to COVID‐19 vaccination in patients with sickle cell disease.
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- British Journal of Haematology, 2023, v. 202, n. 5, p. 937, doi. 10.1111/bjh.18899
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Oral anti‐viral therapy for early COVID‐19 infection in patients with haematological malignancies: A multicentre prospective cohort.
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- British Journal of Haematology, 2023, v. 202, n. 5, p. 928, doi. 10.1111/bjh.18895
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A rare case of acute megakaryoblastic leukaemia with constitutional ring chromosome 21.
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- British Journal of Haematology, 2023, v. 202, n. 5, p. 912, doi. 10.1111/bjh.18892
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Pseudo‐Gaucher cells in a splenectomised Beta‐Thalassemia patient.
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- British Journal of Haematology, 2023, v. 202, n. 5, p. 911, doi. 10.1111/bjh.18890
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Treatment‐free remission after dasatinib in patients with chronic myeloid leukaemia in chronic phase with deep molecular response: Final 5‐year analysis of DASFREE.
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- British Journal of Haematology, 2023, v. 202, n. 5, p. 942, doi. 10.1111/bjh.18883
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Tacrolimus prevents complement‐mediated Nod‐like receptor family pyrin domain containing 3 (NLRP3) inflammasome activation and pyroptosis of mesenchymal stem cells from immune thrombocytopenia.
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- British Journal of Haematology, 2023, v. 202, n. 5, p. 995, doi. 10.1111/bjh.18625
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Issue Information.
- Published in:
- British Journal of Haematology, 2023, v. 202, n. 5, p. 907, doi. 10.1111/bjh.18266
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- Article
KIT D816V is dimerization‐independent and activates downstream pathways frequently perturbed in mastocytosis.
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- British Journal of Haematology, 2023, v. 202, n. 5, p. 960, doi. 10.1111/bjh.18116
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