"Afibrinogenemia" 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 deficiency or absence of FIBRINOGEN in the blood.
| Descriptor ID |
D000347
|
| MeSH Number(s) |
C15.378.100.100.056 C15.378.100.141.072 C15.378.463.067 C16.320.099.056
|
| Concept/Terms |
Afibrinogenemia- Afibrinogenemia
- Afibrinogenemias
- Fibrinogen Deficiency
- Deficiency, Fibrinogen
- Fibrinogen Deficiencies
Congenital Afibrinogenemia- Congenital Afibrinogenemia
- Afibrinogenemia, Congenital
- Afibrinogenemias, Congenital
- Congenital Afibrinogenemias
- Familial Afibrinogenemia
- Afibrinogenemia, Familial
- Afibrinogenemias, Familial
- Familial Afibrinogenemias
- Congenital Afibrinogenaemia
- Afibrinogenaemia, Congenital
- Afibrinogenaemias, Congenital
- Congenital Afibrinogenaemias
- Hypofibrinogenemia, Congenital
- Congenital Hypofibrinogenemia
- Congenital Hypofibrinogenemias
- Hypofibrinogenemias, Congenital
|
Below are MeSH descriptors whose meaning is more general than "Afibrinogenemia".
Below are MeSH descriptors whose meaning is more specific than "Afibrinogenemia".
This graph shows the total number of publications written about "Afibrinogenemia" by people in this website by year, and whether "Afibrinogenemia" 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 |
|---|
| 2000 | 1 | 0 | 1 |
| 2003 | 0 | 1 | 1 |
| 2005 | 1 | 0 | 1 |
| 2010 | 1 | 0 | 1 |
| 2018 | 1 | 0 | 1 |
| 2019 | 1 | 0 | 1 |
| 2022 | 1 | 0 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Afibrinogenemia" by people in Profiles.
-
Choi S, Mazzeffi MA, Henderson R, Mondal S, Morita Y, Deshpande S, Tanaka KA. The FIBTEM paradox: Do coronary artery bypass grafting patients with high baseline FIBTEM clot firmness need more allogeneic blood transfusion? Transfusion. 2022 10; 62(10):2020-2028.
-
Aoki M, Osaka Y, Ando K, Morita Y. Anesthesia Experience for Tonsillectomy in a Patient With Hypofibrinogenemia: A Case Report. A A Pract. 2019 Apr 15; 12(8):259-260.
-
Signoff JK, Fitzgerald JC, Teachey DT, Balamuth F, Weiss SL. Hypofibrinogenemia Is Associated With Poor Outcome and Secondary Hemophagocytic Lymphohistiocytosis/Macrophage Activation Syndrome in Pediatric Severe Sepsis. Pediatr Crit Care Med. 2018 05; 19(5):397-405.
-
Brennan SO, Davis RL, Conard K, Savo A, Furuya KN. Novel fibrinogen mutation ?314Thr?Pro (fibrinogen AI duPont) associated with hepatic fibrinogen storage disease and hypofibrinogenaemia. Liver Int. 2010 Nov; 30(10):1541-7.
-
Keller MA, Martinez J, Baradet TC, Nagaswami C, Chernysh IN, Borowski MK, Surrey S, Weisel JW. Fibrinogen Philadelphia, a hypodysfibrinogenemia characterized by abnormal polymerization and fibrinogen hypercatabolism due to gamma S378P mutation. Blood. 2005 Apr 15; 105(8):3162-8.
-
Deering SH, Landy HJ, Tchabo N, Kessler C. Hypodysfibrinogenemia during pregnancy, labor, and delivery. Obstet Gynecol. 2003 May; 101(5 Pt 2):1092-4.
-
Margaglione M, Santacroce R, Colaizzo D, Seripa D, Vecchione G, Lupone MR, De Lucia D, Fortina P, Grandone E, Perricone C, Di Minno G. A G-to-A mutation in IVS-3 of the human gamma fibrinogen gene causing afibrinogenemia due to abnormal RNA splicing. Blood. 2000 Oct 01; 96(7):2501-5.