ArticleHaematologica2010
Polymorphic variation within the VWF gene contributes to the failure to detect mutations in patients historically diagnosed with type 1 von Willebrand disease from the MCMDM-1VWD cohort.
Article in Haematologica, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
7 citing papers in PubMed.
- Origin and timing of de novo variants implicated in type 2 von Willebrand disease.Journal of cellular and molecular medicine · 2022Article
- Phenotypic and Genotypic Characterization of von Willebrand Factor Gene (Exon 18 and 20) in Saudi Healthy Individuals.Medical archives (Sarajevo, Bosnia and Herzegovina) · 2020Article
- [The function and clinical value of Von Willebrand factor propeptide].Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi · 2015Article
- Article
- The diagnosis and management of von Willebrand disease: a United Kingdom Haemophilia Centre Doctors Organization guideline approved by the British Committee for Standards in Haematology.British journal of haematology · 2014Review
- Article
- Intracellular storage and regulated secretion of von Willebrand factor in quantitative von Willebrand disease.The Journal of biological chemistry · 2011Article
Corrections and comments
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Authors and funding
10 authors.
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Registered trials
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