von Willebrand Disease, Type 1
"von Willebrand Disease, Type 1" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A subtype of von Willebrand disease that results from a partial deficiency of VON WILLEBRAND FACTOR.
MeSH Number(s)
C15.378.100.100.900.100
C15.378.100.141.900.100
C15.378.463.920.100
C16.320.099.920.100
Below are MeSH descriptors whose meaning is more general than "von Willebrand Disease, Type 1".
Below are MeSH descriptors whose meaning is more specific than "von Willebrand Disease, Type 1".
This graph shows the total number of publications written about "von Willebrand Disease, Type 1" by people in Harvard Catalyst Profiles by year, and whether "von Willebrand Disease, Type 1" was a major or minor topic of these publication.
To see the data from this visualization as text,
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Year | Major Topic | Minor Topic | Total |
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2012 | 1 | 0 | 1 |
2019 | 1 | 0 | 1 |
2022 | 1 | 0 | 1 |
Below are the most recent publications written about "von Willebrand Disease, Type 1" by people in Profiles.
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von Willebrand factor levels in the diagnosis of von Willebrand disease: a systematic review and meta-analysis. Blood Adv. 2022 01 11; 6(1):62-71.
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Quantitative analysis of desmopressin (DDAVP) response in adult patients with type 1 von Willebrand disease. Int J Lab Hematol. 2019 Jun; 41(3):325-330.
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Revascularization Operation for Moyamoya Disease with Concurrent von Willebrand Disease. World Neurosurg. 2017 Dec; 108:991.e17-991.e21.
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Assessment of a cohort of primarily pediatric patients with a presumptive diagnosis of type 1 von Willebrand disease with a novel high shear rate, non-citrated blood flow device. Thromb Res. 2012 Apr; 129(4):e18-24.
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Acquired von Willebrand syndrome type 2A in a JAK2-positive essential thrombocythaemia-affected member of a large von Willebrand disease family with a novel autosomal dominant A1716P mutation. Thromb Haemost. 2011 May; 105(5):921-4.