nad has been researched along with Cyanosis in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 6 (85.71) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (14.29) | 2.80 |
| Authors | Studies |
|---|---|
| Ahmad, W; Basit, S; Khurshid, B; Mahmood, A; Samad, A; Shah, AA; Syed, F; Ullah, A; Ur Rehman, H | 1 |
| BEHLEN, CH; CAWEIN, M; COHN, JE; LAPPAT, EJ | 1 |
| Hearse, DJ; Yellon, DM | 1 |
| Angelopoulos, B; Eleftheriadou, A; Karalis, D; Tsoukantas, A | 1 |
| Hsieh, HS; Jaffe, ER | 1 |
| Davies, HE; Lay, H | 1 |
| Faber, K; Heni, F; Schmidt, K | 1 |
2 review(s) available for nad and Cyanosis
| Article | Year |
|---|---|
The "border zone" in evolving myocardial infarction: controversy or confusion?
Topics: Adenosine Triphosphate; Animals; Cell Survival; Collateral Circulation; Coronary Circulation; Coronary Disease; Cyanosis; Dogs; Electrocardiography; Humans; Hypoxia; Microspheres; Myocardial Contraction; Myocardial Infarction; Myocardium; NAD; Polarography; Rabbits; Rats; Time Factors | 1981 |
DPNH-methemoglobin reductase deficiency and hereditary methemoglobinemia.
Topics: Cyanosis; Electrophoresis; Erythrocytes; Genetic Variation; Hemoglobins; Humans; Metabolism, Inborn Errors; Methemoglobin; Methemoglobinemia; NAD; Oxidation-Reduction; Oxidoreductases | 1971 |
5 other study(ies) available for nad and Cyanosis
| Article | Year |
|---|---|
Molecular Dynamic Simulation Analysis of a Novel Missense Variant in
Topics: Cyanosis; Cytochrome-B(5) Reductase; Humans; Methemoglobinemia; Molecular Dynamics Simulation; Mutation; NAD | 2023 |
HEREDITARY DIAPHORASE DEFICIENCY AND METHEMOGLOBINEMIA.
Topics: Blood Protein Electrophoresis; Cyanosis; Cytochrome-B(5) Reductase; Deficiency Diseases; Dihydrolipoamide Dehydrogenase; Erythrocytes; Genetics, Medical; Glucosephosphate Dehydrogenase; Glutathione; Hemoglobinometry; Humans; Methemoglobinemia; Methylene Blue; NAD; Spectrophotometry | 1964 |
Hereditary methemoglobinemia due to DPNH-methemoglobin reductase deficiency: report of a family.
Topics: Adult; Blood Protein Electrophoresis; Child, Preschool; Cyanosis; Dihydrolipoamide Dehydrogenase; Erythrocytes; Female; Genotype; Hemoglobinometry; Humans; Male; Methemoglobinemia; NAD; Oxidoreductases; Pedigree; Spectrum Analysis; Transaminases | 1967 |
A case of hereditary methaemoglobinaemia.
Topics: Cyanosis; Dihydrolipoamide Dehydrogenase; Humans; Infant, Newborn; Infant, Newborn, Diseases; Male; Metabolism, Inborn Errors; Methemoglobinemia; NAD | 1971 |
[Enterogenons methemoglobinemia caused by heterozygotic deficiency of erythrocytic NADH-methemoglobin reductase].
Topics: Ascorbic Acid; Cyanosis; Dihydrolipoamide Dehydrogenase; Erythrocytes; Female; Heterozygote; Humans; Intestines; Kinetics; Metabolism, Inborn Errors; Methemoglobin; Methemoglobinemia; Middle Aged; NAD; Neomycin | 1974 |