nitroblue tetrazolium has been researched along with Embryopathies in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (66.67) | 18.7374 |
| 1990's | 1 (33.33) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Johansen, KS | 1 |
| Murotsuki, J; Okamura, K; Uehara, S; Yajima, A | 1 |
| Ammälä, P; de la Chapelle, A; Kere, J; Leirisalo-Repo, M; Lindlöf, M; Repo, H; Ristola, M; von Koskull, H | 1 |
3 other study(ies) available for nitroblue tetrazolium and Embryopathies
| Article | Year |
|---|---|
Nitroblue tetrazolium slide test. Use of the phorbol-myristate-acetate-stimulated NBT-reduction slide test for routine and prenatal detection of chronic granulomatous disease and diagnosis of heterozygous carriers.
Topics: Female; Fetal Diseases; Genetic Carrier Screening; Glucose; Granulocytes; Granulomatous Disease, Chronic; Humans; Luminescent Measurements; Male; Nitroblue Tetrazolium; Oxidation-Reduction; Phagocytosis; Pregnancy; Prenatal Diagnosis; Staphylococcus aureus; Tetradecanoylphorbol Acetate; Tetrazolium Salts | 1983 |
[Prenatal diagnosis of chronic granulomatous disease by percutaneous umbilical blood sampling].
Topics: Adult; Blood Specimen Collection; Female; Fetal Blood; Fetal Diseases; Granulomatous Disease, Chronic; Humans; Nitroblue Tetrazolium; Pregnancy; Prenatal Diagnosis | 1993 |
Prenatal diagnosis of X-linked chronic granulomatous disease using restriction fragment length polymorphism analysis.
Topics: DNA; Dosage Compensation, Genetic; Female; Fetal Diseases; Genetic Linkage; Genetic Markers; Granulocytes; Granulomatous Disease, Chronic; Humans; Infant; Male; Nitroblue Tetrazolium; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Pregnancy; Prenatal Diagnosis; X Chromosome | 1987 |