"Hemorrhagic Disorders" 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.
Spontaneous or near spontaneous bleeding caused by a defect in clotting mechanisms (BLOOD COAGULATION DISORDERS) or another abnormality causing a structural flaw in the blood vessels (HEMOSTATIC DISORDERS).
| Descriptor ID |
D006474
|
| MeSH Number(s) |
C15.378.463
|
| Concept/Terms |
Hemorrhagic Disorders- Hemorrhagic Disorders
- Disorder, Hemorrhagic
- Disorders, Hemorrhagic
- Hemorrhagic Disorder
- Hemorrhagic Diathesis
- Diatheses, Hemorrhagic
- Diathesis, Hemorrhagic
- Hemorrhagic Diatheses
|
Below are MeSH descriptors whose meaning is more general than "Hemorrhagic Disorders".
Below are MeSH descriptors whose meaning is more specific than "Hemorrhagic Disorders".
This graph shows the total number of publications written about "Hemorrhagic Disorders" by people in this website by year, and whether "Hemorrhagic Disorders" 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 |
|---|
| 2002 | 1 | 1 | 2 |
| 2017 | 0 | 1 | 1 |
| 2019 | 1 | 0 | 1 |
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click here.
Below are the most recent publications written about "Hemorrhagic Disorders" by people in Profiles.
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Alberelli MA, Bacci M, Marchetti M, Ferrazzi P, Dragani A, Gamba S, Landolfi R, Falanga A, Lodigiani C, De Candia E. Rituximab for treatment of autoimmune acquired platelet function disorders: description of two cases of acquired Glanzmann thrombasthenia and one case of acquired delta storage pool disease. Br J Haematol. 2019 12; 187(5):e87-e91.
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Poole LG, Massey VL, Siow DL, Torres-Gonzáles E, Warner NL, Luyendyk JP, Ritzenthaler JD, Roman J, Arteel GE. Plasminogen Activator Inhibitor-1 Is Critical in Alcohol-Enhanced Acute Lung Injury in Mice. Am J Respir Cell Mol Biol. 2017 09; 57(3):315-323.
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Peyvandi F, De Cristofaro R, Akhavan S, Carew JA, Landolfi R, Bauer KA, Mannucci PM. Two naturally occurring mutations on FVII gene (S363I-W364C) altering intrinsic catalytic activity. Thromb Haemost. 2002 Nov; 88(5):750-5.
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Akhavan S, De Cristofaro R, Peyvandi F, Lavoretano S, Landolfi R, Mannucci PM. Molecular and functional characterization of a natural homozygous Arg67His mutation in the prothrombin gene of a patient with a severe procoagulant defect contrasting with a mild hemorrhagic phenotype. Blood. 2002 Aug 15; 100(4):1347-53.