s 2366 has been researched along with Hemophilia B in 1 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) [MeSH]
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (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 |
|---|---|
| Briseid, K; Haug, K; Hoem, NO; Johannesen, S | 1 |
1 other study(ies) available for s 2366 and Hemophilia B
| Article | Year |
|---|---|
Amidolytic assay of factor XI in human plasma--significance of kallikrein for the activity measured.
Topics: Adult; Contraceptives, Oral; Enzyme Activation; Factor XI; Factor XIa; Factor XII; Factor XII Deficiency; Female; Hemophilia B; Humans; Kallikreins; Kininogens; Male; Oligopeptides; Plant Proteins; Prekallikrein; Protease Inhibitors; Pyrrolidonecarboxylic Acid; Trypsin Inhibitors | 1995 |