cytosine has been researched along with Hemophilia B in 2 studies
Hemophilia B: A deficiency of blood coagulation factor IX inherited as an X-linked disorder. (Also known as Christmas Disease, after the first patient studied in detail, not the holy day.) Historical and clinical features resemble those in classic hemophilia (HEMOPHILIA A), but patients present with fewer symptoms. Severity of bleeding is usually similar in members of a single family. Many patients are asymptomatic until the hemostatic system is stressed by surgery or trauma. Treatment is similar to that for hemophilia A. (From Cecil Textbook of Medicine, 19th ed, p1008)
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 2 (100.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Nguyen, P | 1 |
Cornillet, P | 1 |
Potron, G | 1 |
Bottema, CD | 1 |
Bottema, MJ | 1 |
Ketterling, RP | 1 |
Yoon, HS | 1 |
Janco, RL | 1 |
Phillips, JA | 1 |
Sommer, SS | 1 |
2 other studies available for cytosine and Hemophilia B
Article | Year |
---|---|
A new case of severe hemophilia B Leyden, associated with a G to C mutation at position -6 of the factor IX promoter.
Topics: Child; Cytosine; Factor IX; Female; Guanine; Hemophilia B; Humans; Male; Mutation; Promoter Regions, | 1995 |
Why does the human factor IX gene have a G + C content of 40%?
Topics: Base Composition; Biological Evolution; Cytosine; Dinucleoside Phosphates; Factor IX; Guanine; Haplo | 1991 |