nadp has been researched along with Jaundice, Neonatal in 7 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 5 (71.43) | 18.7374 |
1990's | 2 (28.57) | 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 |
---|---|
KOSOY, MH; NAIMAN, JL | 1 |
Cantú, JM; Vaca, G; Velázquez, AL | 1 |
Chen, F; Wu, Z; Zhang, Y | 1 |
Itoh, S; Onishi, S | 1 |
Agar, NS; Harley, JD; Yoshida, A | 1 |
Curreri, R; Marino, S; Russo, A; Russo, G; Schiliro, G; Sciotto, A | 1 |
Corash, LM; Jaffé, ER; Piomelli, S; Rattazzi, MC; van Zanen, GE | 1 |
1 review(s) available for nadp and Jaundice, Neonatal
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 |
6 other study(ies) available for nadp and Jaundice, Neonatal
Article | Year |
---|---|
RED CELL GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY--A NEWLY RECOGNIZED CAUSE OF NEONATAL JAUNDICE AND KERNICTERUS IN CANADA.
Topics: Analgesics; Analgesics, Non-Narcotic; Antimalarials; Antipyretics; Asian People; Biochemical Phenomena; Biochemistry; Canada; Drug Therapy; Erythrocytes; Ethnology; Exchange Transfusion, Whole Blood; Genetics, Medical; Glucosephosphate Dehydrogenase Deficiency; Glucosephosphates; Hemolysis; Humans; Hyperbilirubinemia; Infant, Newborn; Infant, Newborn, Diseases; Jaundice; Jaundice, Neonatal; Kernicterus; Male; Methemoglobin; NADP; Naphthalenes; Nitrofurans; Sex; Statistics as Topic; Sulfanilamide; Sulfanilamides; Sulfonamides; Toxicology; White People | 1964 |
[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 |
[The role of NADPH in the development of neonatal jaundice with G6PD deficiency].
Topics: Glucosephosphate Dehydrogenase Deficiency; Humans; Infant, Newborn; Jaundice, Neonatal; NADP | 1997 |
Glucose 6-phosphate dehydrogenase variants: Gd (+) Alexandra associated with neonatal jaundice and Gd (-) Camperdown in a young man with lamellar cataracts.
Topics: Adolescent; Adult; Cataract; Erythrocytes; Favism; Genetic Variation; Glucosephosphate Dehydrogenase; Glucosephosphate Dehydrogenase Deficiency; Humans; Infant, Newborn; Jaundice, Neonatal; Male; NADP | 1978 |
Glucose-6-phosphate dehydrogenase deficiency in Sicily. Incidence, biochemical characteristics and clinical implications.
Topics: Adolescent; Blood Platelets; Child; Erythrocytes; Favism; Glucosephosphate Dehydrogenase; Glucosephosphate Dehydrogenase Deficiency; Humans; Infant, Newborn; Jaundice, Neonatal; Leukocytes; Male; NADP; Saliva; Sicily | 1979 |
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 |