Page last updated: 2024-10-20

uric acid and Hemophilia A

uric acid has been researched along with Hemophilia A in 2 studies

Uric Acid: An oxidation product, via XANTHINE OXIDASE, of oxypurines such as XANTHINE and HYPOXANTHINE. It is the final oxidation product of purine catabolism in humans and primates, whereas in most other mammals URATE OXIDASE further oxidizes it to ALLANTOIN.
uric acid : An oxopurine that is the final oxidation product of purine metabolism.
6-hydroxy-1H-purine-2,8(7H,9H)-dione : A tautomer of uric acid having oxo groups at C-2 and C-8 and a hydroxy group at C-6.
7,9-dihydro-1H-purine-2,6,8(3H)-trione : An oxopurine in which the purine ring is substituted by oxo groups at positions 2, 6, and 8.

Hemophilia A: 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.

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19902 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Sandhoff, K1
Van Creveld, S1
Pascha, CN1

Other Studies

2 other studies available for uric acid and Hemophilia A

ArticleYear
[Molecular bases of congenital metabolic disorders].
    Verhandlungen der Deutschen Gesellschaft fur Pathologie, 1982, Volume: 66

    Topics: Ascorbic Acid Deficiency; Biological Transport; Female; Gangliosidoses; Glucose-6-Phosphatase; Hemop

1982
Influence of the prostaglandins E1 and E2 on aggregation of blood platelets.
    Nature, 1968, Apr-27, Volume: 218, Issue:5139

    Topics: Adenine Nucleotides; Blood Platelets; Female; Hemophilia A; Humans; Male; Prostaglandins; Uric Acid;

1968