Cargando…
Association between INADL genetic variant and a subgroup with high risk for TMD in the OPPERA study
Autores principales: | Smith, Shad B, Bair, Eric, Xue, Wei, Slade, Gary D, Dubner, Ronald, Fillingim, Roger B, Greenspan, Joel D, Ohrbach, Richard, Knott, Charlie, Diatchenko, Luda, Maixner, William |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4304399/ http://dx.doi.org/10.1186/1744-8069-10-S1-P5 |
Ejemplares similares
-
Translational research in the genomic era: OPPERA study
por: Diatchenko, Luda
Publicado: (2014) -
Anatomical selectivity in overlap of chronic facial and bodily pain
por: Slade, Gary D., et al.
Publicado: (2019) -
COMT Genotype and Efficacy of Propranolol for TMD
Pain: A Randomized Trial
por: Slade, G.D., et al.
Publicado: (2020) -
COMT gene locus: new functional variants
por: Meloto, Carolina B., et al.
Publicado: (2015) -
Effect of comorbid migraine on propranolol efficacy for painful TMD in a randomized controlled trial
por: Tchivileva, Inna E, et al.
Publicado: (2021)