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R Redding-Lallinger

Showing results (1-10 of 9) with videos related to

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American Journal of Hematology|April 1, 1987
Nutrition and sickle cell diseaseJ D Reed, R Redding-Lallinger, E P Orringer
Journal of Tropical Pediatrics|December 1, 1993
An assessment of the use of anthropometric measures for predicting low birth weightJ A Ngowi, R Redding-Lallinger, K F Hirji
Acta Haematologica|September 24, 2010
A new sickling variant 'Hb S-Wake β[(Glu6Val-Asn139 Ser)]' found in a compound heterozygote with Hb S β(Glu6Val) coinherited with homozygous α-thalassemia-2: phenotype and molecular characteristicsFerdane Kutlar, R Redding-Lallinger, S E Meiler, et al.
Journal of Pediatric Psychology|March 22, 2001
Daily coping practice predicts treatment effects in children with sickle cell diseaseK M Gil, K K Anthony, J W Carson, et al.
International Journal of Behavioral Medicine|January 1, 1997
Cognitive coping skills training in children with sickle cell disease painK M Gil, J J Wilson, J L Edens, et al.
AIDS (London, England)|February 1, 1993
Intestinal parasites and HIV infection in Tanzanian children with chronic diarrheaJ P Cegielski, A E Msengi, C S Dukes, et al.
Blood|September 9, 1999
Safety of hydroxyurea in children with sickle cell anemia: results of the HUG-KIDS study, a phase I/II trial. Pediatric Hydroxyurea GroupT R Kinney, R W Helms, E E O'Branski, et al.
British Journal of Haematology|January 17, 2007
Effect of myeloablative bone marrow transplantation on growth in children with sickle cell anaemia: results of the multicenter study of haematopoietic cell transplantation for sickle cell anaemiaB Eggleston, M Patience, S Edwards, et al.
Blood|March 9, 2000
Impact of bone marrow transplantation for symptomatic sickle cell disease: an interim report. Multicenter investigation of bone marrow transplantation for sickle cell diseaseM C Walters, R Storb, M Patience, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
American Journal of Hematology|April 1, 1987
Nutrition and sickle cell diseaseJ D Reed, R Redding-Lallinger, E P Orringer
Journal of Tropical Pediatrics|December 1, 1993
An assessment of the use of anthropometric measures for predicting low birth weightJ A Ngowi, R Redding-Lallinger, K F Hirji
Acta Haematologica|September 24, 2010
A new sickling variant 'Hb S-Wake β[(Glu6Val-Asn139 Ser)]' found in a compound heterozygote with Hb S β(Glu6Val) coinherited with homozygous α-thalassemia-2: phenotype and molecular characteristicsFerdane Kutlar, R Redding-Lallinger, S E Meiler, et al.
Journal of Pediatric Psychology|March 22, 2001
Daily coping practice predicts treatment effects in children with sickle cell diseaseK M Gil, K K Anthony, J W Carson, et al.
International Journal of Behavioral Medicine|January 1, 1997
Cognitive coping skills training in children with sickle cell disease painK M Gil, J J Wilson, J L Edens, et al.
AIDS (London, England)|February 1, 1993
Intestinal parasites and HIV infection in Tanzanian children with chronic diarrheaJ P Cegielski, A E Msengi, C S Dukes, et al.
Blood|September 9, 1999
Safety of hydroxyurea in children with sickle cell anemia: results of the HUG-KIDS study, a phase I/II trial. Pediatric Hydroxyurea GroupT R Kinney, R W Helms, E E O'Branski, et al.
British Journal of Haematology|January 17, 2007
Effect of myeloablative bone marrow transplantation on growth in children with sickle cell anaemia: results of the multicenter study of haematopoietic cell transplantation for sickle cell anaemiaB Eggleston, M Patience, S Edwards, et al.
Blood|March 9, 2000
Impact of bone marrow transplantation for symptomatic sickle cell disease: an interim report. Multicenter investigation of bone marrow transplantation for sickle cell diseaseM C Walters, R Storb, M Patience, et al.
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