phenyl acetate has been researched along with Anemia, Sickle Cell in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (57.14) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (14.29) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 2 (28.57) | 2.80 |
| Authors | Studies |
|---|---|
| Chakravorty, S; Clark, CA; DeHaan, M; Dimitriou, D; Downes, M; Drasar, E; Gavlak, J; Gupta, A; Height, S; Hood, AM; Inusa, B; Kawadler, JM; Kirkham, FJ; Kölbel, M; Lawson, S; Leigh, A; Pelidis, M; Rees, DC; Ridout, D; Sahota, S; Stotesbury, H; Trompeter, S; Wilkey, O; Younis, J | 1 |
| Brandow, A; Bryant, V; DeBaun, MR; Embury, SH; Field, JJ; Kassim, A; Matsui, N; Simpson, P; Wilkerson, K; Zhang, L | 1 |
| Blinder, MA; DeBaun, MR; Field, JJ; Knight-Perry, JE; Strunk, RC; Townsend, RR | 1 |
| Dembure, P; Garrick, MD; Guthrie, R | 1 |
| Rising, JA; Sautter, RL; Spicer, SJ | 1 |
| Barnes, MG; Komarmy, L; Novack, AH | 1 |
| DeJong, WW; Grey, R; Miller, C; Milner, PF; Seakins, M; Went, LN | 1 |
2 trial(s) available for phenyl acetate and Anemia, Sickle Cell
| Article | Year |
|---|---|
Study of montelukast in children with sickle cell disease (SMILES): a study protocol for a randomised controlled trial.
Topics: Acetates; Anemia, Sickle Cell; Anti-Inflammatory Agents; Child; Child, Preschool; Cyclopropanes; Humans; Quinolines; Randomized Controlled Trials as Topic; Sulfides | 2021 |
Phase 2 trial of montelukast for prevention of pain in sickle cell disease.
Topics: Acetates; Adolescent; Adult; Anemia, Sickle Cell; Cyclopropanes; Humans; Leukotriene Antagonists; Pain; Quinolines; Sulfides | 2020 |
5 other study(ies) available for phenyl acetate and Anemia, Sickle Cell
| Article | Year |
|---|---|
Urinary cysteinyl leukotriene E4 significantly increases during pain in children and adults with sickle cell disease.
Topics: Acetates; Adolescent; Adult; Anemia, Sickle Cell; Anti-Asthmatic Agents; Asthma; beta-Thalassemia; Biomarkers; Child; Cohort Studies; Cyclopropanes; Female; Fetal Hemoglobin; Hemoglobin C Disease; Heterozygote; Hospitalization; Humans; Ischemia; Leukotriene Antagonists; Leukotriene E4; Male; Pain; Quinolines; Retrospective Studies; Sickle Cell Trait; Sulfides; Young Adult | 2009 |
Sickle-cell anemia and other hemoglobinopathies. Procedures and strategy for screening employing spots of blood on filter paper as specimens.
Topics: Acetates; Adult; Anemia, Sickle Cell; Blood Protein Electrophoresis; Cellulose; Costs and Cost Analysis; Electrophoresis, Disc; Filtration; Globins; Hemoglobin C; Hemoglobin, Sickle; Hemoglobinopathies; Hemoglobins, Abnormal; Humans; Indicators and Reagents; Infant, Newborn; Mass Screening; Methods; Paper; Solubility | 1973 |
Hemoglobin G-Philadelphia-S. A family study of an inherited hybrid hemoglobin.
Topics: Acetates; Adolescent; Adult; Anemia, Sickle Cell; Black or African American; Blood Cell Count; Blood Platelets; Blood Protein Electrophoresis; Cellulose; Child; Child, Preschool; Erythrocyte Count; Female; Genotype; Hematocrit; Hemoglobin, Sickle; Hemoglobinometry; Hemoglobinopathies; Hemoglobins, Abnormal; Humans; Infant; Male; Middle Aged; Pedigree; Phenotype | 1974 |
A comprehensive screening program for hemoglobinopathies.
Topics: Acetates; Anemia, Sickle Cell; Blood Protein Electrophoresis; Cellulose; Electrophoresis, Paper; Hemoglobin C; Hemoglobinopathies; Hemoglobins, Abnormal; Humans; Mass Screening; Volunteers | 1972 |
Hemoglobin O arab in four negro families and its interaction with hemoglobin S and hemoglobin C.
Topics: Acetates; Adolescent; Adult; Agar; Aged; Amino Acids; Anemia, Sickle Cell; Binding Sites; Black People; Blood Protein Electrophoresis; Cellulose; Child; Child, Preschool; Erythrocytes; Female; Gels; Hemoglobin C; Hemoglobinopathies; Hemoglobins; Hemoglobins, Abnormal; Heterozygote; Homozygote; Humans; Infant; Jamaica; Male; Oxygen; Pedigree; Starch; Thalassemia | 1970 |