Longitudinal bleeding assessment in von Willebrand disease utilizing an interim bleeding score
暂无分享,去创建一个
R. Montgomery | P. Christopherson | P. James | D. Lillicrap | J. Grabell | T. Abshire | S. Haberichter | J. O’Donnell | V. Flood | M. Lavin
[1] R. Mustafa,et al. ASH ISTH NHF WFH 2021 guidelines on the diagnosis of von Willebrand disease. , 2021, Blood advances.
[2] P. James,et al. Significant gynecological bleeding in women with low von Willebrand factor levels. , 2018, Blood advances.
[3] Kenneth L. Jones,et al. Novel insights into the clinical phenotype and pathophysiology underlying low VWF levels. , 2017, Blood.
[4] V. Blanchette,et al. Generation and optimization of the self‐administered pediatric bleeding questionnaire and its validation as a screening tool for von Willebrand disease , 2017, Pediatric blood & cancer.
[5] D. Bellissimo,et al. Clinical and laboratory variability in a cohort of patients diagnosed with type 1 VWD in the United States. , 2016, Blood.
[6] F. Leebeek,et al. Bleeding spectrum in children with moderate or severe von Willebrand disease: Relevance of pediatric‐specific bleeding , 2015, American journal of hematology.
[7] Shamim A. Mollah,et al. Normal range of bleeding scores for the ISTH‐BAT: adult and pediatric data from the merging project , 2014, Haemophilia : the official journal of the World Federation of Hemophilia.
[8] P. Mannucci,et al. The bleeding score predicts clinical outcomes and replacement therapy in adults with von Willebrand disease. , 2014, Blood.
[9] P. James,et al. Generation and optimization of the self‐administered bleeding assessment tool and its validation as a screening test for von Willebrand disease , 2013, Haemophilia : the official journal of the World Federation of Hemophilia.
[10] V. Blanchette,et al. The genetics of Canadian type 3 von Willebrand disease: further evidence for co‐dominant inheritance of mutant alleles , 2013, Journal of thrombosis and haemostasis : JTH.
[11] P. James,et al. The evolution and value of bleeding assessment tools , 2012, Journal of thrombosis and haemostasis : JTH.
[12] M. Nijziel,et al. Determinants of bleeding phenotype in adult patients with moderate or severe von Willebrand disease , 2012, Thrombosis and Haemostasis.
[13] A. Tosetto,et al. A comparison between two semi‐quantitative bleeding scales for the diagnosis and assessment of bleeding severity in type 1 von Willebrand disease , 2011, Haemophilia : the official journal of the World Federation of Hemophilia.
[14] B. Coller,et al. ISTH/SSC bleeding assessment tool: a standardized questionnaire and a proposal for a new bleeding score for inherited bleeding disorders , 2010, Journal of thrombosis and haemostasis : JTH.
[15] R. Hoffmann,et al. Common VWF exon 28 polymorphisms in African Americans affecting the VWF activity assay by ristocetin cofactor. , 2010, Blood.
[16] P. James,et al. The prevalence of symptomatic von Willebrand disease in primary care practice , 2010, Journal of thrombosis and haemostasis : JTH.
[17] P. Mannucci,et al. Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor , 2006, Journal of thrombosis and haemostasis : JTH.
[18] A. Tosetto,et al. A quantitative analysis of bleeding symptoms in type 1 von Willebrand disease: results from a multicenter European study (MCMDM‐1 VWD) , 2006, Journal of thrombosis and haemostasis : JTH.
[19] A. Tosetto,et al. The discriminant power of bleeding history for the diagnosis of type 1 von Willebrand disease: an international, multicenter study , 2005, Journal of thrombosis and haemostasis : JTH.
[20] P. Mannucci. How I treat patients with von Willebrand disease. , 2001, Blood.
[21] F Rodeghiero,et al. Epidemiological investigation of the prevalence of von Willebrand's disease. , 1987, Blood.
[22] L. O'Brien,et al. The mutational spectrum of type 1 von Willebrand disease: Results from a Canadian cohort study. , 2007, Blood.