about
Barth syndrome: an X-linked cause of fetal cardiomyopathy and stillbirthInvestigation of alpha nascent polypeptide-associated complex functions in a human CD8(+) T cell ex vivo expansion model using antisense oligonucleotidesBarth syndrome.The clinical features, risk factors and outcome of thrombotic thrombocytopenic purpura occurring after bone marrow transplantation.Long-term outcomes of hematopoietic stem cell transplantation for severe treatment-resistant autoimmune cytopenia in children.Congenital amegakaryocytic thrombocytopenia (CAMT) presenting as severe pancytopenia in the first month of life.Outcome and clinical course of 100 patients with adenovirus infection following bone marrow transplantation.Shwachman-Diamond syndrome: a complex case demonstrating the potential for misdiagnosis as asphyxiating thoracic dystrophy (Jeune syndrome).Dysmorphology of Barth syndrome.Clinical relevance of MRD in children undergoing allogeneic stem cell transplantation for ALL.Bloodspot assay using HPLC-tandem mass spectrometry for detection of Barth syndrome.Quantitative analysis of chimerism after allogeneic bone marrow transplantation using immunomagnetic selection and fluorescent microsatellite PCR.Hematopoietic cell transplantation for inherited metabolic diseases: an overview of outcomes and practice guidelines.Neurological aspects of osteopetrosis.Barth syndrome without tetralinoleoyl cardiolipin deficiency: a possible ameliorated phenotype.The importance of testing for adrenoleucodystrophy in males with idiopathic Addison's diseaseX-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease.Impact of immune modulation with in vivo T-cell depletion and myleoablative total body irradiation conditioning on outcomes after unrelated donor transplantation for childhood acute lymphoblastic leukemiaAdoptive transfer of cytomegalovirus-specific CTL to stem cell transplant patients after selection by HLA-peptide tetramersHematopoietic stem cell transplantation for osteopetrosis.Minimal residual disease (MRD) status prior to allogeneic stem cell transplantation is a powerful predictor for post-transplant outcome in children with ALL.Molecular diagnosis of vascular access device-associated infection in children being treated for cancer or leukaemia.Severe pulmonary hypertension: a frequent complication of stem cell transplantation for malignant infantile osteopetrosis.Human CD8+ CTL recognition and in vitro lysis of herpes simplex virus-infected cells by a non-MHC restricted mechanism.Minimal residual disease analysis for the prediction of relapse in children with standard-risk acute lymphoblastic leukaemia.The use of the polymerase chain reaction to detect minimal residual disease in childhood acute lymphoblastic leukaemia.The significance of detection of minimal residual disease in childhood acute lymphoblastic leukaemia.Malignant infantile osteopetrosis presenting with neonatal hypocalcaemia.Successful mechanical circulatory support for 251 days in a child with intermittent severe neutropenia due to Barth syndrome.A polymerase chain reaction study of the stability of Ig heavy-chain and T-cell receptor delta gene rearrangements between presentation and relapse of childhood B-lineage acute lymphoblastic leukemia.Very long chain fatty acid levels in patients diagnosed with multiple sclerosis.Improved survival in matched unrelated donor transplant for childhood ALL since the introduction of high-resolution matching at HLA class I and II.The impact of transfusion of leucodepleted platelet concentrates on cytomegalovirus disease after allogeneic stem cell transplantation.Excellent outcome of matched unrelated donor transplantation in paediatric aplastic anaemia following failure with immunosuppressive therapy: a United Kingdom multicentre retrospective experience.Outcome of hematopoietic stem cell transplantation for adenosine deaminase-deficient severe combined immunodeficiency.Non-Epstein-Barr virus-associated T-cell lymphoma following cardiac transplantation for Barth syndrome.Successful cord blood transplantation in a patient with malignant infantile osteopetrosis and hemophilia.Cardiolipin and monolysocardiolipin analysis in fibroblasts, lymphocytes, and tissues using high-performance liquid chromatography-mass spectrometry as a diagnostic test for Barth syndrome.Odontoid infiltration and spinal compression in Farber Disease: reversal by haematopoietic stem cell transplantation.Haematopoietic stem cell transplantation for Shwachman-Diamond disease: a study from the European Group for blood and marrow transplantation.
P50
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P50
description
hulumtues
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researcher
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wetenschapper
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հետազոտող
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name
Colin Steward
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Colin Steward
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Colin Steward
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Colin Steward
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Colin Steward
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type
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Colin Steward
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Colin Steward
@en
Colin Steward
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Colin Steward
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Colin Steward
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prefLabel
Colin Steward
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Colin Steward
@en
Colin Steward
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Colin Steward
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Colin Steward
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P106
P21
P31
P496
0000-0001-6291-0710