Page last updated: 2024-08-17

nad and Cyanosis

nad has been researched along with Cyanosis in 7 studies

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19906 (85.71)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's1 (14.29)2.80

Authors

AuthorsStudies
Ahmad, W; Basit, S; Khurshid, B; Mahmood, A; Samad, A; Shah, AA; Syed, F; Ullah, A; Ur Rehman, H1
BEHLEN, CH; CAWEIN, M; COHN, JE; LAPPAT, EJ1
Hearse, DJ; Yellon, DM1
Angelopoulos, B; Eleftheriadou, A; Karalis, D; Tsoukantas, A1
Hsieh, HS; Jaffe, ER1
Davies, HE; Lay, H1
Faber, K; Heni, F; Schmidt, K1

Reviews

2 review(s) available for nad and Cyanosis

ArticleYear
The "border zone" in evolving myocardial infarction: controversy or confusion?
    The American journal of cardiology, 1981, Volume: 47, Issue:6

    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.
    Seminars in hematology, 1971, Volume: 8, Issue:4

    Topics: Cyanosis; Electrophoresis; Erythrocytes; Genetic Variation; Hemoglobins; Humans; Metabolism, Inborn Errors; Methemoglobin; Methemoglobinemia; NAD; Oxidation-Reduction; Oxidoreductases

1971

Other Studies

5 other study(ies) available for nad and Cyanosis

ArticleYear
Molecular Dynamic Simulation Analysis of a Novel Missense Variant in
    Medicina (Kaunas, Lithuania), 2023, Feb-16, Volume: 59, Issue:2

    Topics: Cyanosis; Cytochrome-B(5) Reductase; Humans; Methemoglobinemia; Molecular Dynamics Simulation; Mutation; NAD

2023
HEREDITARY DIAPHORASE DEFICIENCY AND METHEMOGLOBINEMIA.
    Archives of internal medicine, 1964, Volume: 113

    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.
    Acta haematologica, 1967, Volume: 37, Issue:5

    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.
    Australian paediatric journal, 1971, Volume: 7, Issue:4

    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].
    Blut, 1974, Volume: 29, Issue:1

    Topics: Ascorbic Acid; Cyanosis; Dihydrolipoamide Dehydrogenase; Erythrocytes; Female; Heterozygote; Humans; Intestines; Kinetics; Metabolism, Inborn Errors; Methemoglobin; Methemoglobinemia; Middle Aged; NAD; Neomycin

1974