Cargando…

Bleeding phenotype and diagnostic characterization of patients with congenital platelet defects

Phenotypic characterization of congenital platelet defects (CPDs) could help physicians recognize CPD subtypes and can inform on prognostic implications. We report the analyses of the bleeding phenotype and diagnostic characteristics of a large cohort of adult patients with a confirmed CPD. A total...

Descripción completa

Detalles Bibliográficos
Autores principales:	Blaauwgeers, Maaike W., Kruip, Marieke J.H.A., Beckers, Erik A.M., Coppens, Michiel, Eikenboom, Jeroen, van Galen, Karin P.M., Tamminga, Rienk Y.J., Urbanus, Rolf T., Schutgens, Roger E.G.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley & Sons, Inc. 2020
Materias:	Research Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7540397/ https://www.ncbi.nlm.nih.gov/pubmed/32562285 http://dx.doi.org/10.1002/ajh.25910

Ejemplares similares

The limitation of genetic testing in diagnosing patients suspected for congenital platelet defects
por: Blaauwgeers, Maaike W., et al.
Publicado: (2019)

Congenital platelet disorders and health status–related quality of life
por: Blaauwgeers, Maaike W., et al.
Publicado: (2019)

Flow cytometric mepacrine fluorescence can be used for the exclusion of platelet dense granule deficiency
por: van Asten, Ivar, et al.
Publicado: (2019)

Reliability and Feasibility of the Self-Administered ISTH-Bleeding Assessment Tool
por: Punt, Marieke C., et al.
Publicado: (2019)

Prevalence, burden and treatment effects of vaginal bleeding in women with (suspected) congenital platelet disorders throughout life: a cross‐sectional study
por: Punt, Marieke C., et al.
Publicado: (2021)

Professional functioning of young adults with congenital coagulation disorders in the Netherlands
por: Limperg, Perrine F., et al.
Publicado: (2019)

Desmopressin for bleeding in non‐severe hemophilia A: Suboptimal use in a real‐world setting
por: Zwagemaker, Anne‐Fleur, et al.
Publicado: (2022)

Long-term impact of joint bleeds in von Willebrand disease: a nested case-control study
por: van Galen, Karin P.M., et al.
Publicado: (2017)

Health-related quality of life, developmental milestones, and self-esteem in young adults with bleeding disorders
por: Limperg, P. F., et al.
Publicado: (2017)

Glanzmann thrombasthenia complicated by frequent myeloproliferative neoplasm‐related thromboembolism: thrombosis occurring regardless of αIIbβIII integrin deficiency
por: Schutgens, Roger E. G., et al.
Publicado: (2021)

Criteria for low von Willebrand factor diagnosis and risk score to predict future bleeding
por: Atiq, Ferdows, et al.
Publicado: (2021)

Treatment of acquired hemophilia A, a balancing act: results from a 27‐year Dutch cohort study
por: Schep, Sarah J., et al.
Publicado: (2020)

Platelet dysfunction contributes to bleeding complications in patients with probable leptospirosis
por: Tunjungputri, Rahajeng N., et al.
Publicado: (2017)

BMI is an important determinant of VWF and FVIII levels and bleeding phenotype in patients with von Willebrand disease
por: Atiq, Ferdows, et al.
Publicado: (2019)

Platelet degranulation and bleeding phenotype in a large cohort of Von Willebrand disease patients
por: Swinkels, Maurice, et al.
Publicado: (2022)

Clinical outcome of patients with a vitamin K antagonist‐associated bleeding treated with prothrombin complex concentrate
por: Brekelmans, Marjolein P. A., et al.
Publicado: (2017)

Menstrual and obstetrical bleeding in women with inherited platelet receptor defects—A systematic review
por: Punt, Marieke C., et al.
Publicado: (2020)

Desmopressin treatment combined with clotting factor VIII concentrates in patients with non-severe haemophilia A: protocol for a multicentre single-armed trial, the DAVID study
por: Schütte, Lisette M, et al.
Publicado: (2019)

Lupus anticoagulant associates with thrombosis in patients with COVID‐19 admitted to intensive care units: A retrospective cohort study
por: Noordermeer, Tessa, et al.
Publicado: (2022)

In patients with hemophilia, a decreased thrombin generation profile is associated with a severe bleeding phenotype
por: Verhagen, Marieke J.A., et al.
Publicado: (2023)

Design of a Prospective Study on Pharmacokinetic-Guided Dosing of Prophylactic Factor Replacement in Hemophilia A and B (OPTI-CLOT TARGET Study)
por: Goedhart, Tine M.H.J., et al.
Publicado: (2022)

SYMPHONY consortium: Orchestrating personalized treatment for patients with bleeding disorders
por: Cnossen, Marjon H., et al.
Publicado: (2022)

Major differences in clinical presentation, diagnosis and management of men and women with autosomal inherited bleeding disorders
por: Atiq, F., et al.
Publicado: (2021)

High Five for Low Five
por: Schutgens, Roger E.G.
Publicado: (2020)

The Long and Winding Road for New Treatments for Acquired Thrombotic Thrombocytopenic Purpura
por: Schutgens, Roger E.G.
Publicado: (2019)

FXII: The Cuckoo in the Nest
por: Schutgens, Roger E.G.
Publicado: (2018)

Stay Tuned on Statins: The New Panacea?
por: Schutgens, Roger E.G.
Publicado: (2018)

The efficacy of the entire-vial dosing of emicizumab: Real-world evidence on plasma concentrations, bleeds, and drug waste
por: Donners, Anouk A.M.T., et al.
Publicado: (2023)

Multiparameter platelet function analysis of bleeding patients with a prolonged platelet function analyser closure time
por: Heubel‐Moenen, Floor C. J. I., et al.
Publicado: (2022)

ADAMTS‐13 and bleeding phenotype in von Willebrand disease
por: Boender, Johan, et al.
Publicado: (2020)

Occurrence of FVIII Inhibitors in Hemophilia A Patients Following an Institutional Switch to a Third Generation B-Domain-Deleted FVIII
por: Hooimeijer, Louise H, et al.
Publicado: (2023)

The bleeding phenotype in people with nonsevere hemophilia
por: Kloosterman, Fabienne R., et al.
Publicado: (2022)

Aspirin as Thromboprophylaxis in Orthopedic Surgery: A Matter of Perspective
por: Schutgens, Roger E.G., et al.
Publicado: (2023)

Platelet Activation Mechanisms and Consequences of Immune Thrombocytopenia
por: Sun, Siyu, et al.
Publicado: (2021)

Platelet count and indices as postpartum hemorrhage risk factors: a retrospective cohort study
por: van Dijk, Wobke E. M., et al.
Publicado: (2021)

Enhanced hepatic clearance of hyposialylated platelets explains thrombocytopenia in GNE-related macrothrombocytopenia
por: Noordermeer, Tessa, et al.
Publicado: (2022)

Social participation is reduced in type 3 Von Willebrand disease patients and in patients with a severe bleeding phenotype
por: Kempers, Eva K., et al.
Publicado: (2021)

Molecular mechanisms of bleeding disorderassociated GFI1B(Q287*) mutation and its affected pathways in megakaryocytes and platelets
por: van Oorschot, Rinske, et al.
Publicado: (2019)

Predictive value of a bleeding score for postpartum hemorrhage
por: Gillissen, Ada, et al.
Publicado: (2019)

Effect of polypharmacy on bleeding with rivaroxaban versus vitamin K antagonist for treatment of venous thromboembolism
por: Bistervels, Ingrid M., et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_02ple5qu12pkb0ggnlnd1dupi7