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Journal Articles

The use of monoclonal antibodies and flow cytometry in the diagnosis of paroxysmal nocturnal hemoglobinuria

SE Hall, WF Rosse

Blood (1996) 87 (12): 5332–5340.

https://doi.org/10.1182/blood.V87.12.5332.bloodjournal87125332

Published: 1996

Journal Articles

The molecular basis of paroxysmal nocturnal hemoglobinuria

WF Rosse, RE Ware

Blood (1995) 86 (9): 3277–3286.

https://doi.org/10.1182/blood.V86.9.3277.bloodjournal8693277

Published: 1995

Journal Articles

Immunophenotypic analysis of reticulocytes in paroxysmal nocturnal hemoglobinuria

RE Ware, WF Rosse, SE Hall

Blood (1995) 86 (4): 1586–1589.

https://doi.org/10.1182/blood.V86.4.1586.bloodjournal8641586

Published: 1995

Journal Articles

The structure of the urokinase-type plasminogen activator receptor gene

JR Casey, JG Petranka, J Kottra, DE Fleenor, WF Rosse

Blood (1994) 84 (4): 1151–1156.

https://doi.org/10.1182/blood.V84.4.1151.1151

Published: 1994

Journal Articles

Mutations within the Piga gene in patients with paroxysmal nocturnal hemoglobinuria

RE Ware, WF Rosse, TA Howard

Blood (1994) 83 (9): 2418–2422.

https://doi.org/10.1182/blood.V83.9.2418.2418

Published: 1994

Journal Articles

Glycosyl-phosphatidylinositol anchor synthesis in paroxysmal nocturnal hemoglobinuria: partial or complete defect in an early step

J Norris, S Hall, RE Ware, T Kamitani, HM Chang, E Yeh, WF Rosse

Blood (1994) 83 (3): 816–821.

https://doi.org/10.1182/blood.V83.3.816.816

Published: 1994

Journal Articles

Complement-induced vesiculation and exposure of membrane prothrombinase sites in platelets of paroxysmal nocturnal hemoglobinuria

T Wiedmer, SE Hall, TL Ortel, WH Kane, WF Rosse, PJ Sims

Blood (1993) 82 (4): 1192–1196.

https://doi.org/10.1182/blood.V82.4.1192.1192

Published: 1993

Journal Articles

Defective glycosylphosphatidylinositol anchor synthesis in paroxysmal nocturnal hemoglobinuria granulocytes

JF Mahoney, M Urakaze, S Hall, R DeGasperi, HM Chang, E Sugiyama, CD Warren, M Borowitz, A Nicholson-Weller, WF Rosse

Blood (1992) 79 (6): 1400–1403.

https://doi.org/10.1182/blood.V79.6.1400.1400

Published: 1992

Journal Articles

Dr Ham's test revisited [editorial]

WF Rosse

Blood (1991) 78 (3): 547–550.

https://doi.org/10.1182/blood.V78.3.547.547

Published: 1991

Journal Articles

Transfusion and alloimmunization in sickle cell disease. The Cooperative Study of Sickle Cell Disease

WF Rosse, D Gallagher, TR Kinney, O Castro, H Dosik, J Moohr, W Wang, PS Levy

Blood (1990) 76 (7): 1431–1437.

https://doi.org/10.1182/blood.V76.7.1431.1431

Published: 1990

Journal Articles

Phosphatidylinositol-linked proteins and paroxysmal nocturnal hemoglobinuria

WF Rosse

Blood (1990) 75 (8): 1595–1601.

https://doi.org/10.1182/blood.V75.8.1595.1595

Published: 1990

Journal Articles

Evidence that several high-frequency human blood group antigens reside on phosphatidylinositol-linked erythrocyte membrane proteins

MJ Telen, WF Rosse, CJ Parker, MK Moulds, JJ Moulds

Blood (1990) 75 (7): 1404–1407.

https://doi.org/10.1182/blood.V75.7.1404.1404

Published: 1990

Journal Articles

Erythrocyte membrane inhibitor of reactive lysis: effects of phosphatidylinositol-specific phospholipase C on the isolated and cell- associated protein

MH Holguin, LA Wilcox, NJ Bernshaw, WF Rosse, CJ Parker

Blood (1990) 75 (1): 284–289.

https://doi.org/10.1182/blood.V75.1.284.284

Published: 1990

Journal Articles

Pseudo-Bernard-Soulier syndrome: thrombocytopenia caused by autoantibody to platelet glycoprotein Ib

DV Devine, MS Currie, WF Rosse, CS Greenberg

Blood (1987) 70 (2): 428–431.

https://doi.org/10.1182/blood.V70.2.428.428

Published: 1987

Journal Articles

Structural and functional differences between decay-accelerating factor and red cell acetylcholinesterase [published erratum appears in Blood 1987 Jul;70(1):339]

J Sugarman, DV Devine, WF Rosse

Blood (1986) 68 (3): 680–684.

https://doi.org/10.1182/blood.V68.3.680.680

Published: 1986

Journal Articles

Fragment D-dimer levels: an objective marker of vaso-occlusive crisis and other complications of sickle cell disease

DV Devine, TR Kinney, PF Thomas, WF Rosse, CS Greenberg

Blood (1986) 68 (1): 317–319.

https://doi.org/10.1182/blood.V68.1.317.317

Published: 1986

Journal Articles

Separation of the acetylcholinesterase-deficient red cells in paroxysmal nocturnal hemoglobinuria

FL Chow, SE Hall, WF Rosse, MJ Telen

Blood (1986) 67 (4): 893–897.

https://doi.org/10.1182/blood.V67.4.893.893

Published: 1986

Journal Articles

The control of complement activation by the blood cells in paroxysmal nocturnal hemoglobinuria

WF Rosse

Blood (1986) 67 (2): 268–269.

https://doi.org/10.1182/blood.V67.2.268.268

Published: 1986

Journal Articles

The acetylcholinesterase defect in paroxysmal nocturnal hemoglobinuria: evidence that the enzyme is absent from the cell membrane

FL Chow, MJ Telen, WF Rosse

Blood (1985) 66 (4): 940–945.

https://doi.org/10.1182/blood.V66.4.940.940

Published: 1985

Journal Articles

The origin of ABH antigens on human platelets

RA Dunstan, MB Simpson, RW Knowles, WF Rosse

Blood (1985) 65 (3): 615–619.

https://doi.org/10.1182/blood.V65.3.615.615

Published: 1985

NARROW

The use of monoclonal antibodies and flow cytometry in the diagnosis of paroxysmal nocturnal hemoglobinuria

The molecular basis of paroxysmal nocturnal hemoglobinuria

Immunophenotypic analysis of reticulocytes in paroxysmal nocturnal hemoglobinuria

The structure of the urokinase-type plasminogen activator receptor gene

Mutations within the Piga gene in patients with paroxysmal nocturnal hemoglobinuria

Glycosyl-phosphatidylinositol anchor synthesis in paroxysmal nocturnal hemoglobinuria: partial or complete defect in an early step

Complement-induced vesiculation and exposure of membrane prothrombinase sites in platelets of paroxysmal nocturnal hemoglobinuria

Defective glycosylphosphatidylinositol anchor synthesis in paroxysmal nocturnal hemoglobinuria granulocytes

Dr Ham's test revisited [editorial]

Transfusion and alloimmunization in sickle cell disease. The Cooperative Study of Sickle Cell Disease

Phosphatidylinositol-linked proteins and paroxysmal nocturnal hemoglobinuria

Evidence that several high-frequency human blood group antigens reside on phosphatidylinositol-linked erythrocyte membrane proteins

Erythrocyte membrane inhibitor of reactive lysis: effects of phosphatidylinositol-specific phospholipase C on the isolated and cell- associated protein

Pseudo-Bernard-Soulier syndrome: thrombocytopenia caused by autoantibody to platelet glycoprotein Ib

Structural and functional differences between decay-accelerating factor and red cell acetylcholinesterase [published erratum appears in Blood 1987 Jul;70(1):339]

Fragment D-dimer levels: an objective marker of vaso-occlusive crisis and other complications of sickle cell disease

Separation of the acetylcholinesterase-deficient red cells in paroxysmal nocturnal hemoglobinuria

The control of complement activation by the blood cells in paroxysmal nocturnal hemoglobinuria

The acetylcholinesterase defect in paroxysmal nocturnal hemoglobinuria: evidence that the enzyme is absent from the cell membrane

The origin of ABH antigens on human platelets

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American Society of Hematology

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