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R E Ware

Showing results (1-10 of 103) with videos related to

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The American Journal of Dental Science|February 13, 2019
The Greatest Thing in the WorldR E Ware
The Journal of Pediatrics|March 1, 1997
Salmonella infection in sickle cell disease: a clear and present dangerR E Ware
Adolescent Medicine (Philadelphia, Pa.)|December 28, 1999
Autoimmune hemolytic and thrombocytopenic disease in the adolescent patientR E Ware
Journal of Pediatric Hematology/Oncology|October 19, 1999
Physiologic decline in fetal hemoglobin parameters in infants with sickle cell disease: implications for pharmacological interventionS J Marcus, R E Ware
American Journal of Hematology|December 5, 1998
Inherited DNA mutations contributing to thrombotic complications in patients with sickle cell diseaseS A Zimmerman, R E Ware
Blood|November 1, 1995
The molecular basis of paroxysmal nocturnal hemoglobinuriaW F Rosse, R E Ware
Hematology/Oncology Clinics of North America|December 1, 1996
The adolescent with sickle cell anemiaT R Kinney, R E Ware
Blood|October 1, 1993
Phenotypic and clonal analysis of T lymphocytes in childhood immune thrombocytopenic purpuraR E Ware, T A Howard
Journal of Clinical Immunology|July 1, 1994
Elevated numbers of gamma-delta (gamma delta+) T lymphocytes in children with immune thrombocytopenic purpuraR E Ware, T A Howard
Seminars in Hematology|April 2, 1998
Anti-D: mechanisms of actionR E Ware, S A Zimmerman
Pageof 11

Showing results (1-10 of 103) with videos related to

Sort By:
Pageof 11
The American Journal of Dental Science|February 13, 2019
The Greatest Thing in the WorldR E Ware
The Journal of Pediatrics|March 1, 1997
Salmonella infection in sickle cell disease: a clear and present dangerR E Ware
Adolescent Medicine (Philadelphia, Pa.)|December 28, 1999
Autoimmune hemolytic and thrombocytopenic disease in the adolescent patientR E Ware
Journal of Pediatric Hematology/Oncology|October 19, 1999
Physiologic decline in fetal hemoglobin parameters in infants with sickle cell disease: implications for pharmacological interventionS J Marcus, R E Ware
American Journal of Hematology|December 5, 1998
Inherited DNA mutations contributing to thrombotic complications in patients with sickle cell diseaseS A Zimmerman, R E Ware
Blood|November 1, 1995
The molecular basis of paroxysmal nocturnal hemoglobinuriaW F Rosse, R E Ware
Hematology/Oncology Clinics of North America|December 1, 1996
The adolescent with sickle cell anemiaT R Kinney, R E Ware
Blood|October 1, 1993
Phenotypic and clonal analysis of T lymphocytes in childhood immune thrombocytopenic purpuraR E Ware, T A Howard
Journal of Clinical Immunology|July 1, 1994
Elevated numbers of gamma-delta (gamma delta+) T lymphocytes in children with immune thrombocytopenic purpuraR E Ware, T A Howard
Seminars in Hematology|April 2, 1998
Anti-D: mechanisms of actionR E Ware, S A Zimmerman
Pageof 11