alanine has been researched along with von Willebrand Diseases in 3 studies
Alanine: A non-essential amino acid that occurs in high levels in its free state in plasma. It is produced from pyruvate by transamination. It is involved in sugar and acid metabolism, increases IMMUNITY, and provides energy for muscle tissue, BRAIN, and the CENTRAL NERVOUS SYSTEM.
alanine : An alpha-amino acid that consists of propionic acid bearing an amino substituent at position 2.
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 | 2 (66.67) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ahmad, F | 1 |
| Kannan, M | 1 |
| Biswas, A | 1 |
| Saxena, R | 1 |
| Song, KS | 1 |
| Kang, SH | 1 |
| Kang, MS | 1 |
| Park, YS | 1 |
| Choi, JR | 1 |
| Kim, HK | 1 |
| Park, Q | 1 |
| Wang, Y | 1 |
| Zhang, J | 1 |
| Wan, H | 1 |
3 other studies available for alanine and von Willebrand Diseases
| Article | Year |
|---|---|
Impact of 789Ala/Ala genotype on quantitative type of von Willebrand disease.
Topics: Alanine; Blood Coagulation Tests; Case-Control Studies; DNA Mutational Analysis; Female; Genotype; H | 2009 |
von Willebrand disease with G4022A mutation (vWd Sungnam): a case report.
Topics: Alanine; Child; Glycine; Humans; Male; Point Mutation; von Willebrand Diseases; von Willebrand Facto | 1999 |
[Mutation (Ala737-->Glu) in type 2A von Willebrand disease].
Topics: Adult; Alanine; Factor VIII; Female; Glutamates; Humans; Pedigree; Point Mutation; von Willebrand Di | 1999 |