trolamine salicylate has been researched along with Acroosteolysis with Osteoporosis and Changes in Skull and Mandible in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 2 (66.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Flannery, O; Smith, K | 1 |
| Altun, G; Glucksman, MJ; Martignetti, JA; Mosig, R; Sancak, S; Tuysuz, B | 1 |
| Camacho, C; Evans, BR; Glucksman, MJ; Grum-Tokars, V; Lobl, M; Martignetti, CR; Martignetti, JA; Mosig, RA | 1 |
3 other study(ies) available for trolamine salicylate and Acroosteolysis with Osteoporosis and Changes in Skull and Mandible
| Article | Year |
|---|---|
Osteolysis with secondary arthritis of the scaphotrapeziotrapezoid joint in Hajdu-Cheney syndrome: a case report.
Topics: Arthritis; Female; Hajdu-Cheney Syndrome; Humans; Radiography; Wrist Joint; Young Adult | 2014 |
A novel matrix metalloproteinase 2 (MMP2) terminal hemopexin domain mutation in a family with multicentric osteolysis with nodulosis and arthritis with cardiac defects.
Topics: Abnormalities, Multiple; Arthritis; Base Sequence; Binding Sites; Child; Child, Preschool; DNA Mutational Analysis; Family Health; Female; Hajdu-Cheney Syndrome; Heart Defects, Congenital; Hemopexin; Humans; Male; Matrix Metalloproteinase 2; Models, Molecular; Mutation; Pedigree; Protein Structure, Tertiary; Syndrome; Turkey | 2009 |
Mutation of membrane type-1 metalloproteinase, MT1-MMP, causes the multicentric osteolysis and arthritis disease Winchester syndrome.
Topics: Abnormalities, Multiple; Amino Acid Sequence; Arthritis; Contracture; Corneal Opacity; Female; Growth Disorders; Hajdu-Cheney Syndrome; Humans; Matrix Metalloproteinase 14; Models, Molecular; Mutation; Osteolysis; Osteoporosis; Radiography | 2012 |