cytosine has been researched along with von Willebrand Diseases in 2 studies
von Willebrand Diseases: Group of hemorrhagic disorders in which the VON WILLEBRAND FACTOR is either quantitatively or qualitatively abnormal. They are usually inherited as an autosomal dominant trait though rare kindreds are autosomal recessive. Symptoms vary depending on severity and disease type but may include prolonged bleeding time, deficiency of factor VIII, and impaired platelet adhesion.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (50.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Gallinaro, L | 1 |
| Sartorello, F | 1 |
| Pontara, E | 2 |
| Cattini, MG | 1 |
| Bertomoro, A | 1 |
| Bartoloni, L | 1 |
| Pagnan, A | 1 |
| Casonato, A | 2 |
| Gaucher, C | 1 |
| Zucchetto, A | 1 |
| Zerbinati, P | 1 |
| Mazurier, C | 1 |
| Girolami, A | 1 |
2 other studies available for cytosine and von Willebrand Diseases
| Article | Year |
|---|---|
Combined partial exon skipping and cryptic splice site activation as a new molecular mechanism for recessive type 1 von Willebrand disease.
Topics: Adenine; Adult; Blood Coagulation; Blood Coagulation Tests; Blood Platelets; Cytosine; DNA Mutationa | 2006 |
Type 2N von Willebrand disease due to Arg91Gln substitution and a cytosine deletion in exon 18 of the von Willebrand factor gene.
Topics: Arginine; Cytosine; Exons; Female; Gene Deletion; Hemorrhagic Disorders; Heterozygote; Humans; Middl | 1998 |