Blood Coagulation Disorders, Inherited
"Blood Coagulation Disorders, Inherited" 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.
Hemorrhagic and thrombotic disorders that occur as a consequence of inherited abnormalities in blood coagulation.
MeSH Number(s)
C15.378.100.100
C16.320.099
Concept/Terms
Blood Coagulation Disorders, Inherited- Blood Coagulation Disorders, Inherited
- Inherited Blood Coagulation Disorders
- Hereditary Coagulation Disorders
- Coagulation Disorder, Hereditary
- Coagulation Disorders, Hereditary
- Hereditary Coagulation Disorder
- Coagulation Disorders, Inherited
- Inherited Coagulation Disorders
- Coagulation Disorder, Inherited
- Inherited Coagulation Disorder
- Hereditary Blood Coagulation Disorders
Below are MeSH descriptors whose meaning is more general than "Blood Coagulation Disorders, Inherited".
Below are MeSH descriptors whose meaning is more specific than "Blood Coagulation Disorders, Inherited".
This graph shows the total number of publications written about "Blood Coagulation Disorders, Inherited" by people in Harvard Catalyst Profiles by year, and whether "Blood Coagulation Disorders, Inherited" was a major or minor topic of these publication.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2006 | 0 | 1 | 1 |
| 2013 | 1 | 0 | 1 |
| 2015 | 1 | 0 | 1 |
| 2019 | 3 | 0 | 3 |
| 2020 | 1 | 0 | 1 |
| 2021 | 2 | 0 | 2 |
Below are the most recent publications written about "Blood Coagulation Disorders, Inherited" by people in Profiles.
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Inherited Bleeding Disorders. Hematol Oncol Clin North Am. 2021 12; 35(6):xiii-xiv.
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Inherited bleeding disorders in Afghanistan: The current situation amid COVID-19. Haemophilia. 2021 Jul; 27(4):e579-e580.
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A coagulation defect arising from heterozygous premature termination of tissue factor. J Clin Invest. 2020 10 01; 130(10):5302-5312.
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Targeting protease nexin-1, a natural anticoagulant serpin, to control bleeding and improve hemostasis in hemophilia. Blood. 2019 11 07; 134(19):1632-1644.
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Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels. Circulation. 2019 01 29; 139(5):620-635.
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Bone Marrow Morphology Associated With Germline RUNX1 Mutations in Patients With Familial Platelet Disorder With Associated Myeloid Malignancy. Pediatr Dev Pathol. 2019 Jul-Aug; 22(4):315-328.
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Platelet CD34 expression and a/d-granule abnormalities in GFI1B- and RUNX1-related familial bleeding disorders. Blood. 2017 03 23; 129(12):1733-1736.
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Bullying in medically fragile youth: a review of risks, protective factors, and recommendations for medical providers. J Dev Behav Pediatr. 2015 May; 36(4):285-301.
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The hermansky-pudlak syndrome: clinical features and imperatives from an ophthalmic perspective. Semin Ophthalmol. 2013 Sep-Nov; 28(5-6):387-91.
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Laboratory evaluation of hypercoagulability. Clin Lab Med. 2009 Jun; 29(2):339-66.