valine has been researched along with Migraine Disorders in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (50.00) | 29.6817 |
2010's | 2 (50.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Aurilia, C; Barbanti, P; De Marchis, ML; Della-Morte, D; Egeo, G; Fofi, L; Guadagni, F; Ialongo, C; Ludovici, G; Palmirotta, R | 1 |
Jiang, JR; Jin, SQ; Liao, YJ | 1 |
Herzog, A; Herzog, AL; Marziniak, M; Mössner, R; Sommer, C | 1 |
Corral, J; Díaz Ortuño, A; González-Conejero, R; Iniesta, JA; Martínez Navarro, ML; Vicente, V | 1 |
1 review(s) available for valine and Migraine Disorders
Article | Year |
---|---|
The association between COMT Val158Met polymorphism and migraine risk: A meta-analysis.
Topics: Catechol O-Methyltransferase; Genetic Association Studies; Genetic Predisposition to Disease; Humans; Methionine; Migraine Disorders; Polymorphism, Single Nucleotide; Risk Factors; Valine | 2017 |
3 other study(ies) available for valine and Migraine Disorders
Article | Year |
---|---|
Prion protein gene M129V polymorphism and variability in age at migraine onset.
Topics: Adult; Age of Onset; Aged; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Middle Aged; Migraine Disorders; Polymorphism, Genetic; Prions; Retrospective Studies; Statistics as Topic; Valine | 2013 |
Investigation of the functional brain-derived neurotrophic factor gene variant Val66MET in migraine.
Topics: Adult; Aged; Amino Acid Sequence; Amino Acid Substitution; Brain; Brain-Derived Neurotrophic Factor; Case-Control Studies; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Testing; Genotype; Humans; Male; Methionine; Middle Aged; Migraine Disorders; Polymorphism, Genetic; Risk Factors; Valine | 2008 |
Role of factor XIII Val 34 Leu polymorphism in patients with migraine.
Topics: Adult; Aged; Cerebrovascular Disorders; Factor XIII; Female; Genotype; Humans; Leucine; Male; Middle Aged; Migraine Disorders; Polymerase Chain Reaction; Polymorphism, Genetic; Valine | 2001 |