cytosine has been researched along with Methemoglobinemia in 1 studies
Methemoglobinemia: The presence of methemoglobin in the blood, resulting in cyanosis. A small amount of methemoglobin is present in the blood normally, but injury or toxic agents convert a larger proportion of hemoglobin into methemoglobin, which does not function reversibly as an oxygen carrier. Methemoglobinemia may be due to a defect in the enzyme NADH methemoglobin reductase (an autosomal recessive trait) or to an abnormality in hemoglobin M (an autosomal dominant trait). (Dorland, 27th ed)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Kedar, PS | 1 |
| Nadkarni, AH | 1 |
| Phanasgoankar, S | 1 |
| Madkaikar, M | 1 |
| Ghosh, K | 1 |
| Gorakshakar, AC | 1 |
| Colah, RB | 1 |
| Mohanty, D | 1 |
1 other study available for cytosine and Methemoglobinemia
| Article | Year |
|---|---|
Congenital methemoglobinemia caused by Hb-MRatnagiri (beta-63CAT-->TAT, His-->Tyr) in an Indian family.
Topics: Amino Acid Substitution; Child; Chronic Disease; Cyanosis; Cytosine; DNA; Female; Globins; Hemoglobi | 2005 |