Von willebrand disease [NEW TOPIC PAGE]

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Last Posted: Nov 01, 2019

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• 22q and two: 22q11.2 deletion syndrome and coexisting conditions.
  Cohen Jennifer L et al. American journal of medical genetics. Part A 2018 176(10) 2203-2214
• Establishment of diagnostic facilities for autosomal recessive bleeding disorders in Pakistan.
  Naz Arshi et al. Blood advances 2018 2(Suppl 1) 35-38
• Bleeding Disorders in Women: Free Materials
  CDC, 2019
• Utility of Repeat Testing in the Evaluation for von Willebrand Disease in Pediatric Patients.
  Doshi Bhavya S et al. Journal of thrombosis and haemostasis : JTH 2019 Jul
• No. 163-Gynaecological and Obstetric Management of Women With Inherited Bleeding Disorders.
  Demers Christine et al. Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC 2018 Feb 40(2) e91-e103
• The national blueprint for future basic and translational research to understand factor VIII immunogenicity: NHLBI State of the Science Workshop on factor VIII inhibitors.
  Meeks Shannon L et al. Haemophilia : the official journal of the World Federation of Hemophilia 2019 Jul 25(4) 595-602
• The role of genetics in the pathogenesis and diagnosis of type 1 Von Willebrand disease.
  Flood Veronica H et al. Current opinion in hematology 2019 Jun
• Molecular Genetics of von Willebrand Disease in Korean Patients: Novel Variants and Limited Diagnostic Utility of Multiplex Ligation-Dependent Probe Amplification Analyses.
  Kim Hee Jung et al. Annals of laboratory medicine 2019 Nov 39(6) 545-551
• Update on Molecular Testing in von Willebrand Disease.
  Batlle Javier et al. Seminars in thrombosis and hemostasis 2019 Apr
• von Willebrand Disease in Pediatrics: Evaluation and Management.
  O'Brien Sarah H et al. Hematology/oncology clinics of North America 2019 Jun 33(3) 425-438

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