nadp has been researched along with Anemia, Hemolytic, Congenital in 14 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 10 (71.43) | 18.7374 |
| 1990's | 2 (14.29) | 18.2507 |
| 2000's | 1 (7.14) | 29.6817 |
| 2010's | 1 (7.14) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Jun, SH; Lee, K; Park, CM; Song, J; Song, SH | 1 |
| Cantú, JM; Vaca, G; Velázquez, AL | 1 |
| Fujii, H; Hirono, A; Miwa, S; Morisaki, T; Shinogi, M; Takahashi, K; Takegawa, S; Takizawa, T; Tani, K; Teshirogi, T | 1 |
| Estrada, M; García, M; González, R; Gutiérrez, A; Quintero, I | 1 |
| Itoh, S; Onishi, S | 1 |
| Hollán, S; Horányi, M; Karg, E; Németh, I; Pintér, S; Vécsei, L | 1 |
| Gaetani, GD; Kirkman, HN | 1 |
| Yawata, Y | 1 |
| Beutler, E; Forman, L; Gelbart, T; Hartman, K | 1 |
| Miller, DR; Wollman, MR | 1 |
| Drescher, J; Fischer, K; Schröter, W | 1 |
| Itie, R; Orsini, A; Perrimond, H; Vovan, L | 1 |
| Corash, LM; Jaffé, ER; Piomelli, S; Rattazzi, MC; van Zanen, GE | 1 |
| Arese, P; Bosia, A; Gallo, E; Mazza, U; Pescarmona, GP | 1 |
1 review(s) available for nadp and Anemia, Hemolytic, Congenital
| Article | Year |
|---|---|
[Neonatal jaundice, hereditary hemolytic anemia].
Topics: Anemia, Hemolytic, Congenital; Bilirubin; Diagnosis, Differential; Glucosyltransferases; Hemoglobins; Humans; Infant, Newborn; Jaundice, Neonatal; Mutation; NADP; Oxidative Stress; Prognosis | 1998 |
13 other study(ies) available for nadp and Anemia, Hemolytic, Congenital
| Article | Year |
|---|---|
Ultra-performance liquid chromatography-tandem mass spectrometry-based multiplex enzyme assay for six enzymes associated with hereditary hemolytic anemia.
Topics: 5'-Nucleotidase; Adenosine Diphosphate; Anemia, Hemolytic, Congenital; Chromatography, High Pressure Liquid; Enzyme Assays; Glucosephosphate Dehydrogenase; Humans; Linear Models; NADP; Pyruvate Kinase; Reproducibility of Results; Tandem Mass Spectrometry | 2017 |
[Hereditary erythroenzymopathies. I. Biochemical and genetic aspects].
Topics: Anemia, Hemolytic, Congenital; Erythrocytes; Glucose; Glucosephosphate Dehydrogenase Deficiency; Glutathione; Humans; Infant, Newborn; Jaundice, Neonatal; Mutation; NADP; Nucleotides | 1984 |
G6PD Sendagi: a new glucose-6-phosphate dehydrogenase variant associated with congenital hemolytic anemia.
Topics: Anemia, Hemolytic, Congenital; Anemia, Hemolytic, Congenital Nonspherocytic; Child, Preschool; Genetic Variation; Glucosephosphate Dehydrogenase; Humans; Male; NADP | 1983 |
G6PD Varadero. A new variant of glucose-6-phosphate dehydrogenase associated with congenital nonspherocytic hemolytic anemia.
Topics: Anemia, Hemolytic, Congenital; Anemia, Hemolytic, Congenital Nonspherocytic; Child, Preschool; Cuba; Electrophoresis, Starch Gel; Glucosephosphate Dehydrogenase; Glucosephosphate Dehydrogenase Deficiency; Humans; Hydrogen-Ion Concentration; Male; NADP | 1982 |
Diminished blood levels of reduced glutathione and alpha-tocopherol in two triosephosphate isomerase-deficient brothers.
Topics: Adult; Anemia, Hemolytic, Congenital; Antioxidants; beta Carotene; Bilirubin; Carboxyhemoglobin; Carotenoids; Erythrocytes; Glutathione; Glutathione Reductase; Glutathione Transferase; Hemoglobins; Heterozygote; Humans; Lactic Acid; Lactoylglutathione Lyase; Lipid Peroxides; Lycopene; Male; NADP; Nuclear Family; Thiolester Hydrolases; Triose-Phosphate Isomerase; Vitamin A; Vitamin E | 2000 |
Letter: Glucose-6-phosphate deficiency and inhibition by NADPH: a self-contradictory argument.
Topics: Anemia, Hemolytic, Congenital; Erythrocytes; Glucosephosphate Dehydrogenase Deficiency; NADP | 1975 |
[Abnormality of the glycolytic enzymes and erythrocyte membrane in congenital hemolytic anemia].
Topics: Adenosine Deaminase; Adenylate Kinase; Anemia, Hemolytic, Congenital; Cytoskeleton; Electrolytes; Erythrocyte Membrane; Glucosephosphate Dehydrogenase; Humans; NADP | 1990 |
G-6-PD Walter Reed: possible insight into "structural" NADP in G-6-PD.
Topics: Anemia, Hemolytic, Congenital; Anemia, Hemolytic, Congenital Nonspherocytic; Binding Sites; Enzyme Activation; Glucosephosphate Dehydrogenase; Humans; Infant; Kinetics; Male; NADP | 1986 |
A new variant of glucose-6-phosphate dehydrogenase deficiency hereditary hemolytic anemia, G6PD Cornell: erythrocyte, leukocyte, and platelet studies.
Topics: Adult; Anemia, Hemolytic, Congenital; Blood Bactericidal Activity; Blood Glucose; Blood Platelets; Child; Culture Techniques; Densitometry; Electrophoresis, Starch Gel; Erythrocytes; Female; Fibroblasts; Glucosephosphate Dehydrogenase; Glucosephosphate Dehydrogenase Deficiency; Glutathione; Glycolysis; Humans; Lactates; Leukocytes; Male; NADP; Pedigree; Phagocytosis; Platelet Aggregation; Potassium; Pregnancy; Pseudomonas aeruginosa; Sodium; Staphylococcus | 1974 |
[On a rare form of glucose-6-phosphate dehydrogenase deficiency with congenital nonspherocytic hemolytic anemia].
Topics: Anemia, Hemolytic, Congenital; Child; Chromium Isotopes; Erythrocyte Aging; Erythrocytes; Female; Glucosephosphate Dehydrogenase; Glucosephosphate Dehydrogenase Deficiency; Glutathione Reductase; Humans; Male; NADP; Reticulocytes | 1967 |
[Free nucleotides of erythrocytes in anemias in children. Results of 64 examinations].
Topics: Adenine Nucleotides; Adenosine Triphosphate; Anemia, Hemolytic; Anemia, Hemolytic, Congenital; Anemia, Sickle Cell; Child; Chromatography, Ion Exchange; Elliptocytosis, Hereditary; Erythrocytes; Glucosephosphate Dehydrogenase Deficiency; Hemoglobin C; Hemoglobin C Disease; Hemoglobinopathies; Humans; Hypersplenism; Methods; NAD; NADP; Spectrophotometry; Spherocytosis, Hereditary; Thalassemia | 1969 |
G6PD deficiency and chronic hemolysis: four new mutants--relationships between clinical syndrome and enzyme kinetics.
Topics: Adolescent; Adult; Anemia, Hemolytic, Congenital; Cell Survival; Child; Child, Preschool; Chromium Isotopes; Erythrocytes; Exchange Transfusion, Whole Blood; Female; Glucosephosphate Dehydrogenase; Glucosephosphate Dehydrogenase Deficiency; Humans; Infant, Newborn; Jaundice, Neonatal; Male; Mutation; NADP | 1971 |
Red cell glycolysis in a case of 3-phosphoglycerate kinase deficiency.
Topics: Adenosine Diphosphate; Adenosine Triphosphate; Anemia, Hemolytic, Congenital; Erythrocytes; Female; Glycolysis; Hexokinase; Humans; Metabolism, Inborn Errors; Middle Aged; NAD; NADP; Phosphoglycerate Kinase; Pyruvate Kinase | 1973 |