202 results on '"Slatter, M."'
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2. Conditioning Regimens for Hematopoietic Cell Transplantation in Primary Immunodeficiency
3. Haematopoietic Stem Cell Transplantation for Chronic Granulomatous Disease.
4. Use of defibrotide to treat transplant-associated thrombotic microangiopathy: a retrospective study of the Paediatric Diseases and Inborn Errors Working Parties of the European Society of Blood and Marrow Transplantation
5. Treosulfan-based conditioning regimens for allogeneic haematopoietic stem cell transplantation in children with non-malignant diseases
6. Endothelial cell damage in idiopathic pneumonia syndrome following haematopoietic stem cell transplantation for primary immunodeficiency: AB57
7. Recent advances in the management of graft-versus-host disease
8. Outcome of children requiring intensive care following haematopoietic SCT for primary immunodeficiency and other non-malignant disorders
9. Single centre experience of haematopoietic SCT for patients with immunodysregulation, polyendocrinopathy, enteropathy, X-linked syndrome
10. TREATMENT OF STEROID-REFRACTORY SKIN GRAFT VERSUS HOST DISEASE WITH A CD3 TCR AB/CD19-DEPLETED HAPLO-IDENTICAL HSCT: PH-AB233
11. NON-PTLD MALIGNANCY POST-HSCT FOR PRIMARY IMMUNODEFICIENCY-4 CASES: PH-AB122
12. INTERNATIONAL STUDY ON OUTCOMES OF HAEMATOPOIETIC STEM CELL TRANSPLANT FOR DNA-DSB REPAIR DEFECTS.: PH-P575
13. PHARMACOKINETICS OF HIGH DOSE INTRAVENOUS TREOSULFAN IN CHILDREN PRIOR TO ALLOGENEIC HCT: PH-P584
14. HAEMATOPOIETIC STEM CELL TRANSPLANTATION FOR RAG1/2 SEVERE COMBINED IMMUNODEFICIENCY OR OMENN SYNDROME: A SINGLE CENTRE EXPERIENCE: PH-P559
15. COMMON GAMMA CHAIN- AND JAK3-DEFICIENT SCID, CONDITIONED VERSUS UNCONDITIONED TRANSPLANT: A SINGLE CENTRE EXPERIENCE: PH-P558
16. UK EXPERIENCE OF UNRELATED CORD BLOOD TRANSPLANTATION IN PAEDIATRIC PATIENTS: PH-P540
17. TREATMENT OF STEROID-REFRACTORY GRAFT VERSUS HOST DISEASE (SR-GVHD) AFTER BONE MARROW TRANSPLANT (BMT) FOR PRIMARY IMMUNE DEFICIENCY-SINGLE CENTRE EXPERIENCE: PH-P385
18. TREOSULFAN, FLUDARABINE AND ALEMTUZUMAB CONDITIONING FOR HEMATOPOIETIC STEM CELL TRANSPLANTATION IN CHILDREN WITH PRIMARY IMMUNODEFICIENCY: UK EXPERIENCE: PH-O082
19. The United Kingdom Primary Immune Deficiency (UKPID) Registry: report of the first 4 yearsʼ activity 2008-2012
20. Value of bronchoalveolar lavage before haematopoietic stem cell transplantation for primary immunodeficiency or autoimmune diseases
21. Single centre experience of umbilical cord stem cell transplantation for primary immunodeficiency
22. Outcome of boost haemopoietic stem cell transplant for decreased donor chimerism or graft dysfunction in primary immunodeficiency
23. Thyroid dysfunction after bone marrow transplantation for primary immunodeficiency without the use of total body irradiation in conditioning
24. Polysaccharide antibody responses are impaired post bone marrow transplantation for severe combined immunodeficiency, but not other primary immunodeficiencies
25. Reticular dysgenesis: international survey on clinical presentation, transplantation and outcome: O336
26. Absence of natural killer cells in severe combined immunodeficiency affords a permissive environment for donor T-cell engraftment following non-conditioned allogeneic SCT: O334
27. Outcome of haematopoeitic stem cell transplantation for RAG1/2-deficient severe combined immunodeficiency or Omenn syndrome: P618
28. Immune reconstitution post umbilical cord blood stem cell transplantation for primary immunodeficiency in a national centre: O185
29. Low-dose busulfan/full-dose fludarabine-based reduced-intensity conditioning in 30 high-risk paediatric and adult chronic granulomatous disease patients: O170
30. Nutritional assessment of children undergoing haematopoietic stem cell transplantation for primary immunodeficiency or severe autoimmune disease: R1279
31. Outcome in patients with severe combined immunodeficiency diagnosed at birth in comparison with proband siblings: the case for neonatal screening: O413
32. Mutations in CHD7 in patients with CHARGE syndrome cause T–B + natural killer cell + severe combined immune deficiency and may cause Omenn-like syndrome
33. Clinical Immunology Review Series: An approach to the patient with recurrent infections in childhood
34. Single-centre experience of treosulfan containing conditioning regimens in haematopoeitic stem cell transplantation for primary immunodeficiency
35. Haematopoeitic stem cell transplantation for chronic granulomatous disease - a single-centre experience
36. Clinical spectrum of immunodeficiency, centromeric instability and facial dysmorphism (ICF syndrome)
37. Use of Two Unrelated Umbilical Cord Stem Cell Units in Stem Cell Transplantation for Wiskott–Aldrich Syndrome
38. Successful umbilical cord blood stem cell transplantation for chronic granulomatous disease
39. Bone marrow transplantation for IPEX-like syndrome: 3.6
40. Manifestations of Autoimmune Lymphoproliferative Syndrome: 3.5
41. In utero transplantation: baby steps towards an effective therapy
42. Outcome of bone marrow transplantation in severe combined immunodeficiency with central nervous system viral infection
43. Use of two unrelated umbilical cord stem cell units in stem cell transplantation for Wiskott Aldrich syndrome
44. Outcome of boost haemopoietic stem cell transplant for decrease in donor chimerism or graft dysfunction in primary immunodeficiency
45. Successful bone marrow transplantation for immunodeficiency, centromere instability and facial anomalies syndrome
46. The United Kingdom Primary Immune Deficiency (UKPID) registry 2012 to 2017.
47. Immune Reconstitution and Clinical Outcome After HSCT Infusion for Severe Combined Immunodeficiency in Newcastle
48. Treosulfan, Fludarabine and Alemtuzumab Conditioning for Hematopoietic Stem Cell Transplantation in Children with Primary Immunodeficiency: UK Experience
49. Variants of the VDR gene and risk of colon cancer (United States).
50. Haematopoietic Stem Cell Transplantation For DNA-DSB Repair Defects Using A Modified Fanconi Anaemia Conditioning Regimen
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