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ISTH 2021 Congress

Platelet Disorders, von Willebrand Disease and Thrombotic Microangiopathies

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  • ISTH 2021 Congress
    • Platelet Disorders, von Willebrand Disease and Thrombotic Microangiopathies
      • Acquired Thrombocytopenias
      • ADAMTS13 and TTP
      • Antiplatelet Therapy
      • HIT
      • HUS
      • Inherited Thrombocytopenias
      • Non HUS/TTP Microangiopathies
      • Platelet Antagonists and Novel Therapeutics
      • Platelet Function Disorders, Acquired
      • Platelet Function Disorders, Hereditary
      • von Willebrand Factor Biology
      • VWF and von Willebrand Factor Disorders - Clinical Conditions

Abstract Number: PB0821

A Multicenter Double-blind, Double-dummy, Randomized Study of rhTPO vs Eltrombopag in the Treatment of Chinese Immune Thrombocytopenia

H. Mei1, M. Xu1, G. Yuan2, F. Zhu3, J. Guo4, R. Huang5, J. Qin6, T. Lv2, F. Qin3, H. Cai4, P. Yin7, T. Qin7, Y. Hu1

Abstract Number: PB0857

A Multicenter Retrospective Evaluation of Direct Oral Anticoagulants for the Treatment of Heparin Induced Thrombocytopenia

K. Davis1, J. Sebaaly2, L. Wooten3, C. Khouli4, A. Mihm1, S. Nisly1,5

Abstract Number: PB0904

A Novel Disease-causing Variant in the GP1BA Gene Related to Bernard Soulier Syndrome

A.I. Woods1, M.F. Alberto2, D.M. Primrose3, J. Paiva4, M. Asencio4, M.M. Casinelli4, A.N Blanco4, A. Sánchez-Luceros4,5

Abstract Number: PB0880

A Novel Dual AntiPlatelet and AntiCoagulant APAC: Interaction Between Platelet Factor 4 (PF4) and APAC Decreases Functional Activity

I. Nevzorov1, A. Jouppila2, R. Lassila3,4

Abstract Number: PB0896

A Novel Hemizygous Variant in GATA1 Associated with Bleeding Diathesis and Platelet Dysfunction in Two Unrelated Patients

J.M. Bastida1,2,3,4, D. Boeckelmann5,6, V. Palma-Barqueros7,8, M. Wolter5,6, M.L Lozano7,8, H. Glonnegger5,6, R. Benito2,3, F.H Schilling9, N. Morgan10, K. Freson11, J. Rivera7,8,4, B. Zieger5,6

Abstract Number: PB0863

A Puzzling HIT History: HIT Associated with Fondaparinux or True Autoimmune HIT?

N. Sillamy1, C. Vayne1,2, J. Rollin1,2, M. Desailly1, M. Navarro3, J.-B. Valentin1, C. Pouplard1,2, Y. Gruel1,2

Abstract Number: PB0933

A Quantitative Evaluation of vWF Multimeric Structure in Patients with Different Types of vWD and aVWS

A. Poletaev1, E. Seregina1,2, N. Karamyan1, P. Zharkov1

Abstract Number: PO156

A Refractory Thrombotic Thrombocytopenic Purpura Case Complicated by Hepatic Sinusoidal Obstruction Syndrome and Successful Management with Defibrotide

S. Erdem1, M. Mastanzade1, S. Altay-Dadin2, M. Yanasik3, S. Kalayoglu-Besisik1

Abstract Number: OC 47.2

A Thrombospondin-1 Release Assay (TRA) Coupled to PF4-treated Frozen Platelets is Highly Accurate for the Detection of Pathogenic HIT Antibodies: Implications for Development of a Near-patient HIT in vitro Diagnostic Assay

A. Padmanabhan1, B. Singh1, C. Jones2, R. Leger1, R. Pruthi1, N. Heikal1, D. Chen1

Abstract Number: PB0952

Acquired von Willebrand Disease

M. Escobar1, K. Chong2, N. Montanez1

Abstract Number: PB0938

Acquired von Willebrand Disease: The Diagnosis and Management of an Underdiagnosed Coagulopathy

A. Ferretti1, E. Baldacci1, S. Lancellotti2, M. Basso2, F. Barone2, A. Pallotta3, G. Lapietra1, M. Sacco2, A. Chistolini1, E. De Candia2, C. Santoro1

Abstract Number: PB0888

Acquired δ-Storage Pool Disorder Co-existing with Acquired Factor V Deficiency in Myelodysplastic Syndrome / Myeloproliferative Neoplasm

R. Dave1, J. Mammen1, T. Geevar1, J. Rasalam1, R. Vijayan1, A. Samuel1, S. Singh1, S. Nair1, L. Mathew1

Abstract Number: LPB0031

Activity and Cleavage of von Willebrand Disease Type 2B Variants

M. Brehm1, Y. Yildiz2, T. Obser1, A. Mojzisch1, S. Peine3, S. Schneppenheim4, U. Budde4, R. Schneppenheim5

Abstract Number: PB0909

Age-specific Changes in von Willebrand Factor Multimers in Healthy Children and Adults

N. Letunica1, S. Van Den Helm1, R. Barton1,2,3, V. Karlaftis1,2, P. Monagle3,2,1, V. Ignjatovic2,1.

Abstract Number: PB0907

Agglomeration and then Capture within 10 ms Creates Shear-induced Platelet Aggregation Controlled by von Willebrand Factor Concentration

Z. Liu1, C. Bresette1, C. Aidun1, D. Ku1

Abstract Number: PB0820

Altered Hemostatic Potential in Adults with Primary ITP

T. Schramm1, J. Machacek1, M. Fillitz2, B. Dixer2, D. Mehic1, S. Koder1, C. Ay1, I. Pabinger1, J. Gebhart1

Abstract Number: OC 53.4

Anti-ADAMTS13 Antibodies in Patients with Hereditary Thrombotic Thrombocytopenic Purpura (hTTP)

S.R. Heeb1,2, M. Schaller1,2, E. Tarasco1,2, J.A. Kremer Hovinga1,2

Abstract Number: OC 66.2

Anti-cysteine/Spacer Autoantibodies that Open the Conformation of ADAMTS13 Are a Common Feature of the Autoimmune Response in Immune-mediated Thrombotic Thrombocytopenic Purpura

L. De Waele1, A. Curie1,2, K. Kangro1,3, E. Tellier4, G. Kaplanski4,5, A. Männik3, C. Tersteeg1, B.S. Joly6, P. Coppo7, A. Veyradier6, S.F. De Meyer1, E. Roose1, K. Vanhoorelbeke1

Abstract Number: PO162

Anti-lymphoma Therapy Improves Thrombocytopenia in a Young Patient with Hodgkin Lymphoma: A Case Report

M. Yang1, Z. Zhou2

Abstract Number: PB0853

Arginine-containing Peptides and Acetylsalicylic Acid: Evaluation of Antiplatelet Effects

M. Grigorjeva1, T. Obergan1, T. Shubina1, L. Lyapina1

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