arginine has been researched along with Cervical Fusion Syndrome in 1 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Fleming, J; Gerritsen, J; Graham, GE; Jabs, EW; Lowry, RB | 1 |
1 other study(ies) available for arginine and Cervical Fusion Syndrome
Article | Year |
---|---|
Syndrome of coronal craniosynostosis, Klippel-Feil anomaly, and sprengel shoulder with and without Pro250Arg mutation in the FGFR3 gene.
Topics: Adult; Arginine; Child, Preschool; Craniosynostoses; Facies; Family Health; Female; Humans; Klippel-Feil Syndrome; Male; Mutation; Pedigree; Point Mutation; Proline; Protein-Tyrosine Kinases; Receptor, Fibroblast Growth Factor, Type 3; Receptors, Fibroblast Growth Factor; Shoulder; Syndrome | 2001 |