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R E Ware

Showing results (71-80 of 103) with videos related to

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British Journal of Haematology|February 23, 1999
Erythrocyte autoantibodies in paediatric patients with sickle cell disease receiving transfusion therapy: frequency, characteristics and significanceS M Castellino, M R Combs, S A Zimmerman, et al.
American Journal of Hematology|January 1, 1997
Quantitative analysis of erythrocytes containing fetal hemoglobin (F cells) in children with sickle cell diseaseS J Marcus, T R Kinney, W H Schultz, et al.
Medical and Pediatric Oncology|January 1, 1996
Elevated levels of tumor necrosis factor-beta, gamma-interferon, and IL-6 mRNA in Castleman's diseaseS S Winter, T A Howard, A K Ritchey, et al.
Journal of Pediatric Hematology/Oncology|March 7, 2002
Influence of bilirubin uridine diphosphate-glucuronosyltransferase 1A promoter polymorphisms on serum bilirubin levels and cholelithiasis in children with sickle cell anemiaR G Passon, T A Howard, S A Zimmerman, et al.
The Journal of Thoracic and Cardiovascular Surgery|October 1, 1973
Penetrating cardiac wounds. Significant residual and delayed sequelaeP N Symbas, D A DiOrio, D H Tyras, et al.
The Journal of Rheumatology|March 15, 2001
Effects of inherited thrombophilic mutations in an adolescent with antiphospholipid syndrome and systemic lupus erythematosusE A Higginbotham, S A Zimmerman, T A Howard, et al.
Blood|October 27, 1998
Identification of mutations and polymorphisms in the factor XI genes of an African American family by dideoxyfingerprintingD Martincic, S A Zimmerman, R E Ware, et al.
Blood|September 25, 1998
The PIG-A mutation and absence of glycosylphosphatidylinositol-linked proteins do not confer resistance to apoptosis in paroxysmal nocturnal hemoglobinuriaR E Ware, J Nishimura, M A Moody, et al.
Blood|February 1, 1994
Glycosyl-phosphatidylinositol anchor synthesis in paroxysmal nocturnal hemoglobinuria: partial or complete defect in an early stepJ Norris, S Hall, R E Ware, et al.
Journal of Pediatric Surgery|April 16, 1998
Successful surgical outcome in children with sickle hemoglobinopathies: the Duke University experienceD M Adams, R E Ware, W H Schultz, et al.
Pageof 11

Showing results (71-80 of 103) with videos related to

Sort By:
Pageof 11
British Journal of Haematology|February 23, 1999
Erythrocyte autoantibodies in paediatric patients with sickle cell disease receiving transfusion therapy: frequency, characteristics and significanceS M Castellino, M R Combs, S A Zimmerman, et al.
American Journal of Hematology|January 1, 1997
Quantitative analysis of erythrocytes containing fetal hemoglobin (F cells) in children with sickle cell diseaseS J Marcus, T R Kinney, W H Schultz, et al.
Medical and Pediatric Oncology|January 1, 1996
Elevated levels of tumor necrosis factor-beta, gamma-interferon, and IL-6 mRNA in Castleman's diseaseS S Winter, T A Howard, A K Ritchey, et al.
Journal of Pediatric Hematology/Oncology|March 7, 2002
Influence of bilirubin uridine diphosphate-glucuronosyltransferase 1A promoter polymorphisms on serum bilirubin levels and cholelithiasis in children with sickle cell anemiaR G Passon, T A Howard, S A Zimmerman, et al.
The Journal of Thoracic and Cardiovascular Surgery|October 1, 1973
Penetrating cardiac wounds. Significant residual and delayed sequelaeP N Symbas, D A DiOrio, D H Tyras, et al.
The Journal of Rheumatology|March 15, 2001
Effects of inherited thrombophilic mutations in an adolescent with antiphospholipid syndrome and systemic lupus erythematosusE A Higginbotham, S A Zimmerman, T A Howard, et al.
Blood|October 27, 1998
Identification of mutations and polymorphisms in the factor XI genes of an African American family by dideoxyfingerprintingD Martincic, S A Zimmerman, R E Ware, et al.
Blood|September 25, 1998
The PIG-A mutation and absence of glycosylphosphatidylinositol-linked proteins do not confer resistance to apoptosis in paroxysmal nocturnal hemoglobinuriaR E Ware, J Nishimura, M A Moody, et al.
Blood|February 1, 1994
Glycosyl-phosphatidylinositol anchor synthesis in paroxysmal nocturnal hemoglobinuria: partial or complete defect in an early stepJ Norris, S Hall, R E Ware, et al.
Journal of Pediatric Surgery|April 16, 1998
Successful surgical outcome in children with sickle hemoglobinopathies: the Duke University experienceD M Adams, R E Ware, W H Schultz, et al.
Pageof 11