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Hematopathology and Molecular Hematology
|
December 9, 1998
Paroxysmal nocturnal hemoglobinuria: molecular pathogenesis and molecular therapeutic approaches
J Nishimura, C A Smith, K L Phillips, et al.
Transplantation
|
October 27, 1994
Novel mechanisms of brequinar sodium immunosuppression on T cell activation
T 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 contusion
R 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 haemoglobinuria
M 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 imaging
G 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 haemoglobinuria
M 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 hemoglobinuria
D B Purow, T A Howard, S J Marcus, et al.
Immunology Today
|
April 22, 1999
Research directions in paroxysmal nocturnal hemoglobinuria
D E Dunn, R E Ware, C J Parker, et al.
The Journal of Pediatrics
|
January 1, 1992
Laparoscopic cholecystectomy in young patients with sickle hemoglobinopathies
R 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 disease
D R Wigfall, R E Ware, M R Burchinal, et al.
Page
of 11
Search research articles
Search
Showing results (61-70 of 103) with videos related to
Sort By:
Page
of 11
Hematopathology and Molecular Hematology
|
December 9, 1998
Paroxysmal nocturnal hemoglobinuria: molecular pathogenesis and molecular therapeutic approaches
J Nishimura, C A Smith, K L Phillips, et al.
Transplantation
|
October 27, 1994
Novel mechanisms of brequinar sodium immunosuppression on T cell activation
T 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 contusion
R 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 haemoglobinuria
M 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 imaging
G 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 haemoglobinuria
M 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 hemoglobinuria
D B Purow, T A Howard, S J Marcus, et al.
Immunology Today
|
April 22, 1999
Research directions in paroxysmal nocturnal hemoglobinuria
D E Dunn, R E Ware, C J Parker, et al.
The Journal of Pediatrics
|
January 1, 1992
Laparoscopic cholecystectomy in young patients with sickle hemoglobinopathies
R 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 disease
D R Wigfall, R E Ware, M R Burchinal, et al.
Page
of 11