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Journal Articles

Proteolysis of von Willebrand factor in therapeutic plasma concentrates

PM Mannuccio, A Lattuada, ZM Ruggeri

Blood (1994) 83 (10): 3018–3027.

https://doi.org/10.1182/blood.V83.10.3018.3018

Published: 1994

Journal Articles

Elevated platelet count as a cause of abnormal von Willebrand factor multimer distribution in plasma

U Budde, RE Scharf, P Franke, K Hartmann-Budde, J Dent, ZM Ruggeri

Blood (1993) 82 (6): 1749–1757.

https://doi.org/10.1182/blood.V82.6.1749.1749

Published: 1993

Journal Articles

Real-time analysis of shear-dependent thrombus formation and its blockade by inhibitors of von Willebrand factor binding to platelets

BR Alevriadou, JL Moake, NA Turner, ZM Ruggeri, BJ Folie, MD Phillips, AB Schreiber, ME Hrinda, LV McIntire

Blood (1993) 81 (5): 1263–1276.

https://doi.org/10.1182/blood.V81.5.1263.1263

Published: 1993

Journal Articles

Genetic and structural characterization of an amino acid dimorphism in glycoprotein Ib alpha involved in platelet transfusion refractoriness

M Murata, K Furihata, F Ishida, SR Russell, J Ware, ZM Ruggeri

Blood (1992) 79 (11): 3086–3090.

https://doi.org/10.1182/blood.V79.11.3086.3086

Published: 1992

Journal Articles

von Willebrand factor competes with fibrin for occupancy of GPIIb:IIIa on thrombin-stimulated platelets

RR Hantgan, WL Nichols, ZM Ruggeri

Blood (1990) 75 (4): 889–894.

https://doi.org/10.1182/blood.V75.4.889.889

Published: 1990

Journal Articles

A new congenital platelet abnormality characterized by spontaneous platelet aggregation, enhanced von Willebrand factor platelet interaction, and the presence of all von Willebrand factor multimers in plasma

A Casonato, L De Marco, M Mazzucato, V De Angelis, D De Roia, F Fabris, ZM Ruggeri, A Girolami

Blood (1989) 74 (6): 2028–2033.

https://doi.org/10.1182/blood.V74.6.2028.2028

Published: 1989

Journal Articles

Unique interactions of asialo von Willebrand factor with platelets in platelet-type von Willebrand disease

JL Miller, ZM Ruggeri, VA Lyle

Blood (1987) 70 (6): 1804–1809.

https://doi.org/10.1182/blood.V70.6.1804.1804

Published: 1987

Journal Articles

The von willebrand factor domain-mediating botrocetin-induced binding to glycoprotein IB lies between Val449 and Lys728

Y Fujimura, LZ Holland, ZM Ruggeri, TS Zimmerman

Blood (1987) 70 (4): 985–988.

https://doi.org/10.1182/blood.V70.4.985.985

Published: 1987

Journal Articles

von Willebrand factor and von Willebrand disease [published erratum appears in Blood 1988 Mar;71(3):830]

ZM Ruggeri, TS Zimmerman

Blood (1987) 70 (4): 895–904.

https://doi.org/10.1182/blood.V70.4.895.895

Published: 1987

Journal Articles

Increased surface expression of the membrane glycoprotein IIb/IIIa complex induced by platelet activation. Relationship to the binding of fibrinogen and platelet aggregation

K Niiya, E Hodson, R Bader, V Byers-Ward, JA Koziol, EF Plow, ZM Ruggeri

Blood (1987) 70 (2): 475–483.

https://doi.org/10.1182/blood.V70.2.475.475

Published: 1987

Journal Articles

Proteolytic degradation of von Willebrand factor after DDAVP administration in normal individuals

J Batlle, MF Lopez-Fernandez, A Lopez-Borrasca, C Lopez-Berges, JA Dent, SD Berkowitz, ZM Ruggeri, TS Zimmerman

Blood (1987) 70 (1): 173–176.

https://doi.org/10.1182/blood.V70.1.173.173

Published: 1987

Journal Articles

The heterogeneity of type IIA von Willebrand's disease: studies with protease inhibitors

J Batlle, MF Lopez Fernandez, M Campos, B Justica, C Berges, JL Navarro, JM Diaz Cremades, CK Kasper, JA Dent, ZM Ruggeri

Blood (1986) 68 (6): 1207–1212.

https://doi.org/10.1182/blood.V68.6.1207.1207

Published: 1986

Journal Articles

Subunit composition of plasma von Willebrand factor in patients with the myeloproliferative syndrome

U Budde, JA Dent, SD Berkowitz, ZM Ruggeri, TS Zimmerman

Blood (1986) 68 (6): 1213–1217.

https://doi.org/10.1182/blood.V68.6.1213.1213

Published: 1986

Journal Articles

A new variant of type II von Willebrand disease with aberrant multimeric structure of plasma but not platelet von Willebrand factor (type IIF)

PM Mannucci, R Lombardi, AB Federici, JA Dent, TS Zimmerman, ZM Ruggeri

Blood (1986) 68 (1): 269–274.

https://doi.org/10.1182/blood.V68.1.269.269

Published: 1986

Journal Articles

Separation of human megakaryocytes by state of differentiation on continuous gradients of Percoll: size and ploidy analysis of cells identified by monoclonal antibody to glycoprotein IIb/IIIa

T Ishibashi, ZM Ruggeri, LA Harker, SA Burstein

Blood (1986) 67 (5): 1286–1292.

https://doi.org/10.1182/blood.V67.5.1286.1286

Published: 1986

Journal Articles

High-resolution analysis of von Willebrand factor multimeric composition defines a new variant of type I von Willebrand disease with aberrant structure but presence of all size multimers (type IC)

G Ciavarella, N Ciavarella, S Antoncecchi, D De Mattia, P Ranieri, J Dent, TS Zimmerman, ZM Ruggeri

Blood (1985) 66 (6): 1423–1429.

https://doi.org/10.1182/blood.V66.6.1423.1423

Published: 1985

Journal Articles

Type IIB Tampa: a variant of von Willebrand disease with chronic thrombocytopenia, circulating platelet aggregates, and spontaneous platelet aggregation

HI Saba, SR Saba, J Dent, ZM Ruggeri, TS Zimmerman

Blood (1985) 66 (2): 282–286.

https://doi.org/10.1182/blood.V66.2.282.282

Published: 1985

Journal Articles

Further characterization of platelet-type von Willebrand's disease in Japan

H Takahashi, M Handa, K Watanabe, Y Ando, R Nagayama, A Hattori, A Shibata, AB Federici, ZM Ruggeri, TS Zimmerman

Blood (1984) 64 (6): 1254–1262.

https://doi.org/10.1182/blood.V64.6.1254.1254

Published: 1984

Journal Articles

DDAVP enhances platelet adherence and platelet aggregate growth on human artery subendothelium

KS Sakariassen, M Cattaneo, A v.d. Berg, ZM Ruggeri, PM Mannucci, JJ Sixma

Blood (1984) 64 (1): 229–236.

https://doi.org/10.1182/blood.V64.1.229.229

Published: 1984

Journal Articles

The effect of DDAVP on plasma levels of von Willebrand antigen II in normal individuals and patients with von Willebrand's disease

DR McCarroll, ZM Ruggeri, RR Montgomery

Blood (1984) 63 (3): 532–535.

https://doi.org/10.1182/blood.V63.3.532.532

Published: 1984

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Proteolysis of von Willebrand factor in therapeutic plasma concentrates

Elevated platelet count as a cause of abnormal von Willebrand factor multimer distribution in plasma

Real-time analysis of shear-dependent thrombus formation and its blockade by inhibitors of von Willebrand factor binding to platelets

Genetic and structural characterization of an amino acid dimorphism in glycoprotein Ib alpha involved in platelet transfusion refractoriness

von Willebrand factor competes with fibrin for occupancy of GPIIb:IIIa on thrombin-stimulated platelets

A new congenital platelet abnormality characterized by spontaneous platelet aggregation, enhanced von Willebrand factor platelet interaction, and the presence of all von Willebrand factor multimers in plasma

Unique interactions of asialo von Willebrand factor with platelets in platelet-type von Willebrand disease

The von willebrand factor domain-mediating botrocetin-induced binding to glycoprotein IB lies between Val449 and Lys728

von Willebrand factor and von Willebrand disease [published erratum appears in Blood 1988 Mar;71(3):830]

Increased surface expression of the membrane glycoprotein IIb/IIIa complex induced by platelet activation. Relationship to the binding of fibrinogen and platelet aggregation

Proteolytic degradation of von Willebrand factor after DDAVP administration in normal individuals

The heterogeneity of type IIA von Willebrand's disease: studies with protease inhibitors

Subunit composition of plasma von Willebrand factor in patients with the myeloproliferative syndrome

A new variant of type II von Willebrand disease with aberrant multimeric structure of plasma but not platelet von Willebrand factor (type IIF)

Separation of human megakaryocytes by state of differentiation on continuous gradients of Percoll: size and ploidy analysis of cells identified by monoclonal antibody to glycoprotein IIb/IIIa

High-resolution analysis of von Willebrand factor multimeric composition defines a new variant of type I von Willebrand disease with aberrant structure but presence of all size multimers (type IC)

Type IIB Tampa: a variant of von Willebrand disease with chronic thrombocytopenia, circulating platelet aggregates, and spontaneous platelet aggregation

Further characterization of platelet-type von Willebrand's disease in Japan

DDAVP enhances platelet adherence and platelet aggregate growth on human artery subendothelium

The effect of DDAVP on plasma levels of von Willebrand antigen II in normal individuals and patients with von Willebrand's disease

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American Society of Hematology

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American Society of Hematology

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