glutamine has been researched along with Thalassemia in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (60.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (20.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (20.00) | 2.80 |
| Authors | Studies |
|---|---|
| Cappellini, MD; Ferraresi, M; Kattamis, A; Leoni, S; Motta, I; Panzieri, DL | 1 |
| Balduini, CL; De Candia, E; Savoia, A | 1 |
| Gordon, PA; Headlee, ME; Huisman, TH; Lam, H; Rigal, WM; Salkie, ML; Wilson, JB | 1 |
| Dozy, AM; Kan, YW; Lie-Injo, LE; Lopes, M; Todd, D | 1 |
| Chen, CJ; Gottleib, M; Gravely, ME; Huisman, TH; Lindeman, JG; Lutcher, CL; Miller, A; Stevens, PD; Wilson, JB; Wong, SC | 1 |
1 review(s) available for glutamine and Thalassemia
| Article | Year |
|---|---|
Therapeutic perspective for children and young adults living with thalassemia and sickle cell disease.
Topics: Anemia, Sickle Cell; Child; Child, Preschool; Glutamine; Hemoglobinopathies; Humans; Infant; Thalassemia; Young Adult | 2023 |
4 other study(ies) available for glutamine and Thalassemia
| Article | Year |
|---|---|
Why the disorder induced by GATA1 Arg216Gln mutation should be called "X-linked thrombocytopenia with thalassemia" rather than "X-linked gray platelet syndrome".
Topics: Arginine; Blood Platelets; GATA1 Transcription Factor; Genes, X-Linked; Glutamine; Humans; Mutation; Syndrome; Terminology as Topic; Thalassemia; Thrombocytopenia | 2007 |
Hb A2-Canada or alpha 2 delta 2 99(G1) Asp replaced by Asn, a newly discovered delta chain variant with increased oxygen affinity occurring in cis to beta-thalassemia.
Topics: Adolescent; Amino Acid Sequence; Asparaginase; Aspartic Acid; Canada; Child; Female; Glutamine; Hemoglobin A; Hemoglobin A2; Humans; Male; Middle Aged; Oxygen Consumption; Thalassemia | 1982 |
The alpha-globin gene adjacent to the gene for HbQ-alpha 74 Asp replaced by His is deleted, but not that adjacent to the gene for HbG-alpha 30 Glu replaced by Gln; three-fourths of the alpha-globin genes are deleted in HbQ-alpha-thalassemia.
Topics: Aspartic Acid; Chemical Phenomena; Chemistry; Chromosome Deletion; DNA; Genetic Carrier Screening; Globins; Glutamates; Glutamine; Hemoglobin H; Hemoglobins, Abnormal; Histidine; Humans; Hybridization, Genetic; Peptides; Thalassemia | 1979 |
Hb Leslie, an unstable hemoglobin due to deletion of glutaminyl residue beta 131 (H9) occurring in association with beta0-thalassemia, HbC, and HbS.
Topics: Adolescent; Adult; Amino Acid Sequence; Anemia; Child; Child, Preschool; Chromatography, DEAE-Cellulose; Electrophoresis, Starch Gel; Female; Glutamine; Hemoglobin C; Hemoglobin, Sickle; Hemoglobinopathies; Hemoglobins, Abnormal; Humans; Male; Middle Aged; Pedigree; Thalassemia | 1976 |