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P Darbyshire

Showing results (91-100 of 110) with videos related to

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The Journal of Infection|November 1, 1993
Chronic granulomatous disease presenting in childhood with Pseudomonas cepacia septicaemiaD E Lacy, D A Spencer, A Goldstein, et al.
American Journal of Respiratory and Critical Care Medicine|January 1, 1994
Successful treatment of invasive pulmonary aspergillosis in chronic granulomatous disease with orally administered itraconazole suspensionD A Spencer, P John, S R Ferryman, et al.
Acta Paediatrica (Oslo, Norway : 1992)|January 26, 2002
Bone density in the Asian thalassaemic population: a cross-sectional reviewB K Bielinski, P Darbyshire, L Mathers, et al.
Journal of the Royal Society of Medicine|September 1, 1995
Urticaria pigmentosa and acute lymphoblastic leukaemiaH M Lewis, E Winter, P Darbyshire, et al.
British Journal of Haematology|January 1, 1985
Lysosomal isoenzyme profiles used to classify a case of acute undifferentiated leukaemiaO B Eden, P Darbyshire, R M Simpson, et al.
British Journal of Nursing (Mark Allen Publishing)|April 11, 1996
Children's nursing as a research-based professionE A Glasper, C Powell, P Darbyshire, et al.
International Journal of Laboratory Hematology|March 13, 2008
ZAP-70 is highly expressed in most cases of childhood pre-B cell acute lymphoblastic leukemiaF Wandroo, A Bell, P Darbyshire, et al.
Child: Care, Health and Development|December 8, 2009
Health-related quality of life and financial impact of caring for a child with Thalassaemia Major in the UKS A Clarke, R Skinner, J Guest, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|October 19, 2000
Comparison of allogeneic transplant versus chemotherapy for relapsed childhood acute lymphoblastic leukaemia in the MRC UKALL R1 trial. MRC Childhood Leukaemia Working PartyG Harrison, S Richards, S Lawson, et al.
Bone Marrow Transplantation|January 18, 2006
Increased acute GvHD and higher transplant-related mortality in non-caucasians undergoing standard sibling allogeneic stem cell transplantationM Karanth, G Begum, M Cook, et al.
Pageof 11

Showing results (91-100 of 110) with videos related to

Sort By:
Pageof 11
The Journal of Infection|November 1, 1993
Chronic granulomatous disease presenting in childhood with Pseudomonas cepacia septicaemiaD E Lacy, D A Spencer, A Goldstein, et al.
American Journal of Respiratory and Critical Care Medicine|January 1, 1994
Successful treatment of invasive pulmonary aspergillosis in chronic granulomatous disease with orally administered itraconazole suspensionD A Spencer, P John, S R Ferryman, et al.
Acta Paediatrica (Oslo, Norway : 1992)|January 26, 2002
Bone density in the Asian thalassaemic population: a cross-sectional reviewB K Bielinski, P Darbyshire, L Mathers, et al.
Journal of the Royal Society of Medicine|September 1, 1995
Urticaria pigmentosa and acute lymphoblastic leukaemiaH M Lewis, E Winter, P Darbyshire, et al.
British Journal of Haematology|January 1, 1985
Lysosomal isoenzyme profiles used to classify a case of acute undifferentiated leukaemiaO B Eden, P Darbyshire, R M Simpson, et al.
British Journal of Nursing (Mark Allen Publishing)|April 11, 1996
Children's nursing as a research-based professionE A Glasper, C Powell, P Darbyshire, et al.
International Journal of Laboratory Hematology|March 13, 2008
ZAP-70 is highly expressed in most cases of childhood pre-B cell acute lymphoblastic leukemiaF Wandroo, A Bell, P Darbyshire, et al.
Child: Care, Health and Development|December 8, 2009
Health-related quality of life and financial impact of caring for a child with Thalassaemia Major in the UKS A Clarke, R Skinner, J Guest, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|October 19, 2000
Comparison of allogeneic transplant versus chemotherapy for relapsed childhood acute lymphoblastic leukaemia in the MRC UKALL R1 trial. MRC Childhood Leukaemia Working PartyG Harrison, S Richards, S Lawson, et al.
Bone Marrow Transplantation|January 18, 2006
Increased acute GvHD and higher transplant-related mortality in non-caucasians undergoing standard sibling allogeneic stem cell transplantationM Karanth, G Begum, M Cook, et al.
Pageof 11