"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,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2004 | 3 | 0 | 3 |
| 2005 | 1 | 0 | 1 |
| 2006 | 1 | 0 | 1 |
| 2011 | 1 | 1 | 2 |
| 2014 | 2 | 0 | 2 |
| 2016 | 1 | 0 | 1 |
| 2017 | 4 | 0 | 4 |
| 2018 | 1 | 0 | 1 |
| 2019 | 1 | 0 | 1 |
| 2020 | 0 | 1 | 1 |
| 2021 | 1 | 0 | 1 |
| 2022 | 1 | 0 | 1 |
| 2023 | 1 | 0 | 1 |
| 2024 | 2 | 0 | 2 |
| 2025 | 1 | 0 | 1 |
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Below are the most recent publications written about "Hemophilia A" by people in Profiles.
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Emicizumab in pediatric hemophilia: Bleeding and surgical outcomes from a single-center retrospective study. Pediatr Blood Cancer. 2021 11; 68(11):e29325.
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Novel treatment of combined factor V and factor VIII deficiency with Factor Eight Inhibitor Bypass Activity. Haemophilia. 2020 Jan; 26(1):e21-e22.
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Acute, symptomatic catheter-associated DVT with mobile, intra-cardiac thrombus in an infant with severe haemophilia A. Haemophilia. 2014 Mar; 20(2):e182-4.
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Neonatal helper-dependent adenoviral vector gene therapy mediates correction of hemophilia A and tolerance to human factor VIII. Proc Natl Acad Sci U S A. 2011 Feb 01; 108(5):2082-7.
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Neonatal hyperbilirubinemia: an unexpected cause. Clin Pediatr (Phila). 2008 May; 47(4):388-94.
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Mandibular haemophilic pseudotumour containing a fluid-fluid level. Br J Radiol. 2001 Feb; 74(878):186-8.
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Spontaneous isolated lesser sac hematoma in a patient with hemophilia. Indian J Gastroenterol. 1999 Jan-Mar; 18(1):38-9.
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Genetic therapy using bone marrow transplantation. Cancer Treat Res. 1995; 76:271-80.
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Neuropsychologic functioning of human immunodeficiency virus-infected children with hemophilia. J Pediatr. 1993 Jan; 122(1):52-9.
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Defective T suppressor-inducer cell function in human immune deficiency virus-seropositive hemophilia patients. Blood. 1988 Nov; 72(5):1474-7.