bumetanide has been researched along with Anemia, Sickle Cell in 7 studies
Anemia, Sickle Cell: A disease characterized by chronic hemolytic anemia, episodic painful crises, and pathologic involvement of many organs. It is the clinical expression of homozygosity for hemoglobin S.
| Excerpt | Relevance | Reference |
|---|---|---|
| "We describe a population of sickle cell anemia red cells (SS RBCs) ( approximately 4%) and a smaller fraction of normal RBCs (<0." | 1.31 | Identification and characterization of a newly recognized population of high-Na+, low-K+, low-density sickle and normal red cells. ( Bookchin, RM; Etzion, Z; Lew, VL; Mohandas, N; Skepper, JN; Sorette, M, 2000) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (14.29) | 18.7374 |
| 1990's | 4 (57.14) | 18.2507 |
| 2000's | 2 (28.57) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Holtzclaw, JD | 1 |
| Jiang, M | 1 |
| Yasin, Z | 1 |
| Joiner, CH | 1 |
| Franco, RS | 1 |
| Etzion, Z | 2 |
| Lew, VL | 2 |
| Bookchin, RM | 2 |
| Gibson, JS | 1 |
| Speake, PF | 1 |
| Ellory, JC | 3 |
| Sorette, M | 1 |
| Mohandas, N | 1 |
| Skepper, JN | 1 |
| Hall, AC | 2 |
| Ody, SA | 1 |
| Poli de Figueiredos, CE | 1 |
| Chalder, S | 1 |
| Stuart, J | 1 |
| Ody, SO | 1 |
| Englert, HC | 1 |
| Mania, D | 1 |
| Lang, HJ | 1 |
| Brugnara, C | 1 |
| Bunn, HF | 1 |
| Tosteson, DC | 1 |
7 other studies available for bumetanide and Anemia, Sickle Cell
| Article | Year |
|---|---|
Rehydration of high-density sickle erythrocytes in vitro.
Topics: Anemia, Sickle Cell; Bumetanide; Cell Fractionation; Erythrocytes; Fluid Therapy; Homozygote; Humans | 2002 |
K(86Rb) transport heterogeneity in the low-density fraction of sickle cell anemia red blood cells.
Topics: Anemia, Sickle Cell; Biological Transport; Bumetanide; Carrier Proteins; Cell Separation; Erythrocyt | 1996 |
Differential oxygen sensitivity of the K+-Cl- cotransporter in normal and sickle human red blood cells.
Topics: Anemia, Sickle Cell; Bumetanide; Carboxylic Acids; Carrier Proteins; Chlorides; Egtazic Acid; Enzyme | 1998 |
Identification and characterization of a newly recognized population of high-Na+, low-K+, low-density sickle and normal red cells.
Topics: Anemia, Sickle Cell; Bumetanide; Calcimycin; Calcium; Cell Membrane Permeability; Drug Resistance; E | 2000 |
KCl cotransport in HbAA and HbSS red cells: activation by intracellular acidity and disappearance during maturation.
Topics: Anemia, Sickle Cell; Biological Transport; Bumetanide; Carrier Proteins; Choline; Dehydration; Eryth | 1991 |
Selective inhibitors of KCl cotransport in human red cells.
Topics: Anemia, Sickle Cell; Biological Transport; Bumetanide; Erythrocytes; Furosemide; Hemochromatosis; Hu | 1990 |
Regulation of erythrocyte cation and water content in sickle cell anemia.
Topics: Anemia, Sickle Cell; Body Water; Bumetanide; Erythrocytes; Hemoglobin, Sickle; Humans; Hydrogen-Ion | 1986 |