trolamine salicylate has been researched along with 22q11.2 Deletion Syndrome in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (33.33) | 18.7374 |
| 1990's | 1 (33.33) | 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 |
|---|---|
| Cron, RQ; Sullivan, KE | 1 |
| Denman, AM | 1 |
| Athreya, BH; Driscoll, DA; Ellabban, AS; Emanuel, BS; Keenan, G; McDonald-McGinn, DM; Reed, L; Sullivan, KE; Zackai, EH; Zmijewski, CM | 1 |
1 review(s) available for trolamine salicylate and 22q11.2 Deletion Syndrome
| Article | Year |
|---|---|
Immunodeficiency and general medicine.
Topics: Adolescent; Agammaglobulinemia; Arthritis; B-Lymphocytes; Bacterial Infections; Child; Child, Preschool; DiGeorge Syndrome; Female; Granulomatous Disease, Chronic; Humans; IgA Deficiency; Immunologic Deficiency Syndromes; Male; Neutropenia; Purine-Nucleoside Phosphorylase; Respiratory Tract Infections; T-Lymphocytes | 1980 |
2 other study(ies) available for trolamine salicylate and 22q11.2 Deletion Syndrome
| Article | Year |
|---|---|
Chronic arthritis without uveitis in velocardiofacial syndrome.
Topics: Arthritis; Child; Chronic Disease; Diagnosis, Differential; DiGeorge Syndrome; Humans; Prevalence; Uveitis | 2006 |
Juvenile rheumatoid arthritis-like polyarthritis in chromosome 22q11.2 deletion syndrome (DiGeorge anomalad/velocardiofacial syndrome/conotruncal anomaly face syndrome).
Topics: Arthritis; Arthritis, Juvenile; CD8-Positive T-Lymphocytes; Child; Chromosome Deletion; Chromosomes, Human, Pair 22; DiGeorge Syndrome; Female; Humans; Infant; Infant, Newborn; Male; Prevalence | 1997 |