fibrinogen has been researched along with Genetic Diseases, Inborn in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (66.67) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (33.33) | 2.80 |
| Authors | Studies |
|---|---|
| Kowalcze, K; Krysiak, R; Okopień, B | 1 |
| Bayan, K; Canoruc, N; Dursun, M; Tüzün, Y; Yilmaz, S | 1 |
| Cai, H; Hong, J; Hui, R; Li, C; Li, G; Sun, S; Wang, J; Ye, J | 1 |
3 other study(ies) available for fibrinogen and Genetic Diseases, Inborn
| Article | Year |
|---|---|
Cardiometabolic profile of young women with hypoprolactinemia.
Topics: C-Reactive Protein; Cabergoline; Cardiovascular Diseases; Carotid Intima-Media Thickness; Female; Fibrinogen; Genetic Diseases, Inborn; Glucose; Humans; Lactation Disorders; Prolactin; Risk Factors; Uric Acid | 2022 |
Analysis of inherited thrombophilic mutations and natural anticoagulant deficiency in patients with idiopathic portal hypertension.
Topics: Adult; Apolipoprotein E2; Apolipoprotein E3; Apolipoprotein E4; Apolipoproteins B; Factor V; Factor XIII; Female; Fibrinogen; Genetic Diseases, Inborn; Humans; Hypertension, Portal; Integrin beta3; Male; Methylenetetrahydrofolate Reductase (NADPH2); Mutation, Missense; Peptidyl-Dipeptidase A; Prothrombin | 2009 |
[Relationship between calpain-10 gene polymorphism, hypertension and plasma glucose].
Topics: Adult; Age Factors; Blood Glucose; Calpain; Female; Fibrinogen; Gene Frequency; Genetic Diseases, Inborn; Humans; Hyperglycemia; Hypertension; Insulin; Male; Polymorphism, Genetic; Sex Factors; Triglycerides | 2002 |