Search Results - "Gordon‐Smith, E. C."
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1
The effect of treatment with Campath‐1H in patients with autoimmune cytopenias
Published in British journal of haematology (01-09-2001)“…We describe 21 patients with severe and life‐threatening autoimmune cytopenias resistant to standard immunosuppression who were treated with the monoclonal…”
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2
Guidelines for the diagnosis and management of acquired aplastic anaemia
Published in British journal of haematology (01-12-2003)Get full text
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3
Increased apoptosis of bone marrow CD34+ cells and impaired function of bone marrow stromal cells in patients with systemic lupus erythematosus
Published in British journal of haematology (01-10-2001)“…The changes in bone marrow (BM) stem cell reserve and function and stromal cell function in patients with active systemic lupus erythematosus (SLE) were…”
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4
Marrow transplants from matched unrelated donors for aplastic anaemia using alemtuzumab, fludarabine and cyclophosphamide based conditioning
Published in Bone marrow transplantation (Basingstoke) (01-03-2005)“…Graft failure, regimen-related toxicity and graft-versus-host disease (GVHD) are the critical barriers to unrelated donor transplants for aplastic anaemia…”
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5
The role of occupational and environmental exposures in the aetiology of acquired severe aplastic anaemia: a case control investigation
Published in British journal of haematology (01-12-2003)“…Aplastic anaemia is a rare but serious disorder with a high morbidity and mortality rate. The causes of aplastic anaemia are, for the most part, unknown. We…”
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The Use of 7-Amino Actinomycin D in Identifying Apoptosis: Simplicity of Use and Broad Spectrum of Application Compared With Other Techniques
Published in Blood (15-03-1996)“…The detection and quantitation of apoptotic cells is becoming increasingly important in the investigation of the role of apoptosis in cellular proliferation…”
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Diamond-Blackfan anaemia in the U.K.: analysis of 80 cases from a 20-year birth cohort
Published in British journal of haematology (01-09-1996)“…The U.K. Diamond-Blackfan Anaemia (DBA) Registry was established with the aim of providing a representative database for studies on the aetiology,…”
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8
Relapse of severe aplastic anaemia after influenza immunization
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9
Mechanisms of bone marrow progenitor cell apoptosis in aplastic anaemia and the effect of anti-thymocyte globulin : examination of the role of the Fas-Fas-L interaction
Published in British journal of haematology (01-12-2000)“…The mechanism of action of anti-thymocyte globulin (ATG) in aplastic anaemia (AA) is complex. Bone marrow (BM) CD34(+) cells in AA have been shown to be more…”
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10
Bcl‐2 and Bcl‐x expression in the CD34+ cells of aplastic anaemia patients: relationship with increased apoptosis and upregulation of Fas antigen
Published in British journal of haematology (01-06-2001)“…Aplastic anaemia (AA) is a syndrome of haemopoietic failure involving increased apoptosis in stem cells. AA CD34+ cells often have upregulated Fas antigen, but…”
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11
Serum thrombopoietin levels in patients with aplastic anaemia
Published in British journal of haematology (01-12-1996)“…Endogenous serum thrombopoietin (TPO) levels were measured in 31 patients with aplastic anaemia (AA) using an enzyme immunoassay with a sensitivity of 20 pg/…”
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12
The sensitivity of Fanconi anaemia group C cells to apoptosis induced by mitomycin C is due to oxygen radical generation, not DNA crosslinking
Published in British journal of haematology (01-02-1997)“…Fanconi's anaemia (FA) is characterized by increased spontaneous and induced chromosome fragility. This has been widely regarded to be due to a defect in DNA…”
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13
Abnormal cytogenetic clones in patients with aplastic anaemia: response to immunosuppressive therapy
Published in British journal of haematology (01-02-1999)“…We report the response to immunosuppressive therapy with antithymocyte globulin (ATG) and cyclosporin or oxymetholone in 13 cases of aplastic anaemia (AA) with…”
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14
Implications of CD34+ cell dose on clinical and haematological outcome of allo-SCT for acquired aplastic anaemia
Published in Bone marrow transplantation (Basingstoke) (01-05-2010)“…The precise effects of CD34+ cell dose on the outcome of allogeneic transplantation for aplastic anaemia (AA) are not known. Previous studies have used the…”
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15
Lack of clinical efficacy of rituximab in the treatment of autoimmune neutropenia and pure red cell aplasia: implications for their pathophysiology
Published in Annals of hematology (01-03-2007)“…We describe 11 patients with severe refractory autoimmune cytopenias treated with the anti-CD20 monoclonal antibody rituximab. Six patients had autoimmune…”
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16
Remission induced by Campath-1H for thymoma-associated agranulocytosis
Published in Annals of hematology (01-06-2004)“…Thymoma-associated agranulocytosis is a rare but almost universally fatal condition. Reports to date have described several immunosuppressive therapies…”
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17
N-RAS gene mutation in patients with aplastic anemia and aplastic anemia/ paroxysmal nocturnal hemoglobinuria during evolution to clonal disease
Published in Blood (15-01-2000)“…Long-term survivors of aplastic anemia (AA) have a high incidence of clonal disorders, in particular paroxysmal nocturnal hemoglobinuria (PNH), myelodysplastic…”
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18
Study of the association between cytochromes P450 2D6 and 2E1 genotypes and the risk of drug and chemical induced idiosyncratic aplastic anaemia
Published in British journal of haematology (01-02-1999)“…A genetic susceptibility to drug or chemical toxicity may provide a basis for an increased risk of idiosyncratic aplastic anaemia (AA). The cytochrome P450…”
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19
Sustained remission of severe resistant autoimmune neutropenia with Campath‐1H
Published in British journal of haematology (01-05-1997)“…We report the course of a patient with severe autoimmune neutropenia in whom only transient responses occurred with corticosteroids, antilymphocyte globulin…”
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20
Progressive telomere shortening in aplastic anemia
Published in Blood (15-05-1998)“…Improved survival in aplastic anemia (AA) has shown a high incidence of late clonal marrow disorders. To investigate whether accelerated senescence of…”
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