 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.
| Descriptor ID |
D056725
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| 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
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| Concept/Terms |
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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 this website by year, and whether "von Willebrand Disease, Type 1" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2017 | 1 | 0 | 1 |
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Below are the most recent publications written about "von Willebrand Disease, Type 1" by people in Profiles.
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Lehmann M, Ashworth K, Manco-Johnson M, Di Paola J, Neeves KB, Ng CJ. Evaluation of a microfluidic flow assay to screen for von Willebrand disease and low von Willebrand factor levels. J Thromb Haemost. 2018 01; 16(1):104-115.
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Branchford BR, Ruegg K, Villalobos-Menuey E, Jacobson LJ, Di Paola JA, Manco-Johnson M. FVIII/VWF ratio is not a reliable predictor of VWD in children. Pediatr Blood Cancer. 2014 May; 61(5):936-9.
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Flood VH, Friedman KD, Gill JC, Haberichter SL, Christopherson PA, Branchford BR, Hoffmann RG, Abshire TC, Dunn AL, Di Paola JA, Hoots WK, Brown DL, Leissinger C, Lusher JM, Ragni MV, Shapiro AD, Montgomery RR. No increase in bleeding identified in type 1 VWD subjects with D1472H sequence variation. Blood. 2013 May 02; 121(18):3742-4.
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