25 results on '"Wynn, R F"'
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2. Is it congenital or acquired von Willebrands disease?
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3. “WE CAN WORK IT OUT” - THE DEVELOPMENT OF A CONSENSUS APPROACH TO PAEDIATRIC STEM CELL TRANSPLANTATION IN THE UK: PH-O115
4. Chronic norovirus infection in pediatric hematopoietic stem cell transplant recipients: A cause of prolonged intestinal failure requiring intensive nutritional support
5. Multifocal vascular lesions and thrombocytopenia in a 10-year-old boy: retrospective review of a recently recognized rare congenital disorder
6. Inflammatory BCG adenitis associated with immune reconstitution following allogeneic haematopoietic stem cell transplant in infancy
7. The anaesthetic management of children with anterior mediastinal masses
8. Treosulfan-containing regimens achieve high rates of engraftment associated with low transplant morbidity and mortality in children with non-malignant disease and significant co-morbidities
9. Pre-transplant ERT and full intensity transplant in MPSIH: Manchester's data of 15 consecutively transplanted patients: a review of more than 70 transplants for MPSIH and evidence for significant improvement in EFS compared to previous SCT protocols
10. Outcomes of hematopoietic stem cell transplantation for Hurler's syndrome in Europe: a risk factor analysis for graft failure
11. Biochemical monitoring after haemopoietic stem cell transplant for Hurler syndrome (MPSIH): implications for functional outcome after transplant in metabolic disease
12. Haematopoietic cell transplantation (HCT) in combination with enzyme replacement therapy (ERT) in patients with Hurler syndrome
13. Intractable diarrhoea of infancy caused by neutrophil specific granule deficiency and cured by stem cell transplantation
14. Survey on haematopoietic stem cell transplantation for children in Europe
15. Effects of topoisomerase 2 inhibitors on the MLL gene in children receiving chemotherapy: a prospective study
16. Marrow stromal cells from patients affected by MPS I differentially support haematopoietic progenitor cell development
17. Sequential reduced- and full-intensity allografting using same donor in a child with chronic granulomatous disease and coexistent, significant comorbidity
18. Reduced-intensity conditioning in first and second allograft in children without immunodeficiency: experience of three British transplant centres
19. Systemic juvenile idiopathic arthritis, Kikuchiʼs disease and haemophagocytic lymphohistiocytosis
20. Association of acute parvovirus B19 infection with new onset of acute lymphoblastic and myeloblastic leukaemia
21. Systemic juvenile idiopathic arthritis, Kikuchiʼs disease and haemophagocytic lymphohistiocytosis—is there a link? Case report and literature review
22. Prominent dyserythropoiesis in four cases of haemophagocytic lymphohistiocytosis
23. AGGRESSIVE MULTIPLE MODALITY THERAPY FOR VARICELLA-ASSOCIATED PURPURA FULMINANS
24. ASSESSMENT OF A FLOW CYTOMETRIC ASSAY FOR THE DIAGNOSIS OF HEREDITARY SPHEROCYTOSIS IN A PAEDIATRIC HAEMATOLOGY LABORATORY.
25. Paroxysmal cold haemoglobinuria of childhood: a review of the management and unusual presenting features of six cases
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