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R E Ware

Showing results (61-70 of 103) with videos related to

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Hematopathology and Molecular Hematology|December 9, 1998
Paroxysmal nocturnal hemoglobinuria: molecular pathogenesis and molecular therapeutic approachesJ Nishimura, C A Smith, K L Phillips, et al.
Transplantation|October 27, 1994
Novel mechanisms of brequinar sodium immunosuppression on T cell activationT L Forrest, R E Ware, T Howard, et al.
Surgical Forum|January 1, 1972
Coronary arterial injection of radioactive albumin microspheres in diagnosis of experimental myocardial contusionR E Ware, L G Martin, D H Tyras, et al.
British Journal of Haematology|June 1, 1996
Identification and characterization of an inherited mutation of PIG-A in a patient with paroxysmal nocturnal haemoglobinuriaM Endo, R E Ware, T M Vreeke, et al.
Developmental Medicine and Child Neurology|March 1, 1996
Delayed development of sensorineural hearing loss after neonatal hyperbilirubinemia: a case report with brain magnetic resonance imagingG Worley, C W Erwin, R F Goldstein, et al.
British Journal of Haematology|March 1, 1996
Resolution of Budd-Chiari syndrome following bone marrow transplantation for paroxysmal nocturnal haemoglobinuriaM L Graham, W F Rosse, E C Halperin, et al.
Blood Cells, Molecules & Diseases|July 2, 1999
Genetic instability and the etiology of somatic PIG-A mutations in paroxysmal nocturnal hemoglobinuriaD B Purow, T A Howard, S J Marcus, et al.
Immunology Today|April 22, 1999
Research directions in paroxysmal nocturnal hemoglobinuriaD E Dunn, R E Ware, C J Parker, et al.
The Journal of Pediatrics|January 1, 1992
Laparoscopic cholecystectomy in young patients with sickle hemoglobinopathiesR E Ware, T R Kinney, J R Casey, et al.
The Journal of Pediatrics|June 6, 2000
Prevalence and clinical correlates of glomerulopathy in children with sickle cell diseaseD R Wigfall, R E Ware, M R Burchinal, et al.
Pageof 11

Showing results (61-70 of 103) with videos related to

Sort By:
Pageof 11
Hematopathology and Molecular Hematology|December 9, 1998
Paroxysmal nocturnal hemoglobinuria: molecular pathogenesis and molecular therapeutic approachesJ Nishimura, C A Smith, K L Phillips, et al.
Transplantation|October 27, 1994
Novel mechanisms of brequinar sodium immunosuppression on T cell activationT L Forrest, R E Ware, T Howard, et al.
Surgical Forum|January 1, 1972
Coronary arterial injection of radioactive albumin microspheres in diagnosis of experimental myocardial contusionR E Ware, L G Martin, D H Tyras, et al.
British Journal of Haematology|June 1, 1996
Identification and characterization of an inherited mutation of PIG-A in a patient with paroxysmal nocturnal haemoglobinuriaM Endo, R E Ware, T M Vreeke, et al.
Developmental Medicine and Child Neurology|March 1, 1996
Delayed development of sensorineural hearing loss after neonatal hyperbilirubinemia: a case report with brain magnetic resonance imagingG Worley, C W Erwin, R F Goldstein, et al.
British Journal of Haematology|March 1, 1996
Resolution of Budd-Chiari syndrome following bone marrow transplantation for paroxysmal nocturnal haemoglobinuriaM L Graham, W F Rosse, E C Halperin, et al.
Blood Cells, Molecules & Diseases|July 2, 1999
Genetic instability and the etiology of somatic PIG-A mutations in paroxysmal nocturnal hemoglobinuriaD B Purow, T A Howard, S J Marcus, et al.
Immunology Today|April 22, 1999
Research directions in paroxysmal nocturnal hemoglobinuriaD E Dunn, R E Ware, C J Parker, et al.
The Journal of Pediatrics|January 1, 1992
Laparoscopic cholecystectomy in young patients with sickle hemoglobinopathiesR E Ware, T R Kinney, J R Casey, et al.
The Journal of Pediatrics|June 6, 2000
Prevalence and clinical correlates of glomerulopathy in children with sickle cell diseaseD R Wigfall, R E Ware, M R Burchinal, et al.
Pageof 11