L S Lessin|W F Rosse - JoVE Visualize

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Transfusion|January 1, 1984

Acquired alteration in the expression of blood groups in a patient with sideroblastic anemia and chronic renal failureM N Levine, W K Kuhns, T A Bolk, et al.

Blood|April 1, 1990

Evidence that several high-frequency human blood group antigens reside on phosphatidylinositol-linked erythrocyte membrane proteinsM J Telen, W F Rosse, C J Parker, et al.

Blood|July 1, 1986

Fragment D-dimer levels: an objective marker of vaso-occlusive crisis and other complications of sickle cell diseaseD V Devine, T R Kinney, P F Thomas, 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.

The Journal of Clinical Investigation|November 1, 1989

Relationship between the membrane inhibitor of reactive lysis and the erythrocyte phenotypes of paroxysmal nocturnal hemoglobinuriaM H Holguin, L A Wilcox, N J Bernshaw, et al.

Journal of Immunology (Baltimore, Md. : 1950)|October 21, 1998

Production of IgM hexamers by normal and autoimmune B cells: implications for the physiologic role of hexameric IgMC T Hughey, J W Brewer, A D Colosia, et al.

The Journal of Experimental Medicine|June 1, 1988

Identification of human erythrocyte blood group antigens on decay-accelerating factor (DAF) and an erythrocyte phenotype negative for DAFM J Telen, S E Hall, A M Green, 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.

The Journal of Clinical Investigation|July 1, 1987

Relationship between decay accelerating factor deficiency, diminished acetylcholinesterase activity, and defective terminal complement pathway restriction in paroxysmal nocturnal hemoglobinuria erythrocytesM E Medof, A Gottlieb, T Kinoshita, et al.

Pageof 14

Showing results (111-120 of 138) with videos related to

Sort By:

Pageof 14

Transfusion|January 1, 1984

Acquired alteration in the expression of blood groups in a patient with sideroblastic anemia and chronic renal failureM N Levine, W K Kuhns, T A Bolk, et al.

Blood|April 1, 1990

Evidence that several high-frequency human blood group antigens reside on phosphatidylinositol-linked erythrocyte membrane proteinsM J Telen, W F Rosse, C J Parker, et al.

Blood|July 1, 1986

Fragment D-dimer levels: an objective marker of vaso-occlusive crisis and other complications of sickle cell diseaseD V Devine, T R Kinney, P F Thomas, 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.

The Journal of Clinical Investigation|November 1, 1989

Relationship between the membrane inhibitor of reactive lysis and the erythrocyte phenotypes of paroxysmal nocturnal hemoglobinuriaM H Holguin, L A Wilcox, N J Bernshaw, et al.

Journal of Immunology (Baltimore, Md. : 1950)|October 21, 1998

Production of IgM hexamers by normal and autoimmune B cells: implications for the physiologic role of hexameric IgMC T Hughey, J W Brewer, A D Colosia, et al.

The Journal of Experimental Medicine|June 1, 1988

Identification of human erythrocyte blood group antigens on decay-accelerating factor (DAF) and an erythrocyte phenotype negative for DAFM J Telen, S E Hall, A M Green, 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.

The Journal of Clinical Investigation|July 1, 1987

Relationship between decay accelerating factor deficiency, diminished acetylcholinesterase activity, and defective terminal complement pathway restriction in paroxysmal nocturnal hemoglobinuria erythrocytesM E Medof, A Gottlieb, T Kinoshita, et al.

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