"Hemophilia A" 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.
The classic hemophilia resulting from a deficiency of factor VIII. It is an inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhage.
Descriptor ID |
D006467
|
MeSH Number(s) |
C15.378.100.100.500 C15.378.100.141.500 C15.378.463.500 C16.320.099.500
|
Concept/Terms |
Hemophilia A- Hemophilia A
- Hemophilia As
- Hemophilia, Classic
- Hemophilia
- Hemophilia A, Congenital
- Congenital Hemophilia A
- Congenital Hemophilia As
- Hemophilia As, Congenital
- Classic Hemophilia
- Classic Hemophilias
- Hemophilias, Classic
- Haemophilia
Autosomal Hemophilia A- Autosomal Hemophilia A
- As, Autosomal Hemophilia
- Autosomal Hemophilia As
- Hemophilia A, Autosomal
- Hemophilia As, Autosomal
Factor VIII Deficiency- Factor VIII Deficiency
- Factor 8 Deficiency, Congenital
- Factor VIII Deficiency, Congenital
- Deficiency, Factor VIII
|
Below are MeSH descriptors whose meaning is more general than "Hemophilia A".
Below are MeSH descriptors whose meaning is more specific than "Hemophilia A".
This graph shows the total number of publications written about "Hemophilia A" by people in this website by year, and whether "Hemophilia A" was a major or minor topic of these publications.
To see the data from this visualization as text,
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Year | Major Topic | Minor Topic | Total |
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1996 | 0 | 1 | 1 |
2005 | 1 | 0 | 1 |
2011 | 0 | 1 | 1 |
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Below are the most recent publications written about "Hemophilia A" by people in Profiles.
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Halpern LR, Adams DR, Clarkson E. Treatment of the Dental Patient with Bleeding Dyscrasias: Etiologies and Management Options for Surgical Success in Practice. Dent Clin North Am. 2020 04; 64(2):411-434.
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Garc?a Ar?z M, P?rez-Carrasquillo O, Zierenberg CE, Cheleuitte J, Guerra JA, Santiago-Borrero PJ. Hemostatic matrix application after open synovectomy in a hemophilic patient. Am J Orthop (Belle Mead NJ). 2012 Apr; 41(4):179-81.
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Banerjee DK, Oliveira CM, Tav?rez JJ, Katiyar VN, Saha S, Mart?nez JA, Banerjee A, S?nchez A, Baksi K. Importance of a factor VIIIc-like glycoprotein expressed in capillary endothelial cells (eFactor VIIIc) in angiogenesis. Adv Exp Med Biol. 2011; 705:453-64.
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Tenenbaum SA, Morris CA, Alexander SS, McFerrin HE, Garry RF, Leissinger CA. Evidence of HIV exposure and transient seroreactivity in archived HIV-negative severe hemophiliac sera. Virol J. 2005 Aug 17; 2:65.
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Santiago-Borrero PJ, Ortiz I, Rivera-Caragol E, Maldonado NI. Financial aspects of haemophilia care in Puerto Rico and other Latin American countries. Haemophilia. 1999 Nov; 5(6):386-91.
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Rock G, Adamkiewicz T, Blanchette V, Poon A, Sparling C. Acquired von Willebrand factor deficiency during high-dose infusion of recombinant factor VIII. Br J Haematol. 1996 Jun; 93(3):684-7.
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Santiago-Borrero PJ, Casanova R. Response of patients with hemophilia A and von Willebrand disease to desmopressin (DDAVP). Bol Asoc Med P R. 1990 May; 82(5):207-10.