arginine has been researched along with Direct Hyperbilirubinemia, Neonatal in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 3 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Liu, Y; Sun, J; Wang, L; Yu, Z; Zhu, K | 1 |
| Can, G; Çoban, A; Ergen, A; Ince, Z; Isbir, T; Narter, F | 1 |
| Ebell, W; Kühl, JS; Meisel, C; Münch, A; Pekrun, A; Schmugge, M; Schwarz, K; von Bernuth, H; Wahn, V | 1 |
1 review(s) available for arginine and Direct Hyperbilirubinemia, Neonatal
| Article | Year |
|---|---|
Association of Neonatal Hyperbilirubinemia with UGT1A1 Gene Polymorphisms: A Meta-Analysis.
Topics: Algorithms; Arginine; Female; Gene Frequency; Glucuronosyltransferase; Glycine; Humans; Hyperbilirubinemia, Neonatal; Male; Odds Ratio; Polymorphism, Genetic; Promoter Regions, Genetic; Regression Analysis; Risk Factors | 2015 |
2 other study(ies) available for arginine and Direct Hyperbilirubinemia, Neonatal
| Article | Year |
|---|---|
Neonatal hyperbilirubinemia and G71R mutation of the UGT1A1 gene in Turkish patients.
Topics: Amino Acid Substitution; Arginine; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Gestational Age; Glucuronosyltransferase; Glycine; Humans; Hyperbilirubinemia, Neonatal; Infant, Newborn; Male; Polymorphism, Single Nucleotide; Turkey | 2011 |
Hyperbilirubinemia and rapid fatal hepatic failure in severe combined immunodeficiency caused by adenosine deaminase deficiency (ADA-SCID).
Topics: Adenosine Deaminase; Agammaglobulinemia; Amino Acid Substitution; Arginine; Bone Marrow Transplantation; Consanguinity; Exons; Fatal Outcome; Female; Hepatorenal Syndrome; Histidine; Humans; Hyperbilirubinemia, Neonatal; Infant; Infant, Newborn; Leukocyte Count; Liver Failure; Liver Function Tests; Lymphocyte Activation; Mutation, Missense; Neutrophils; Severe Combined Immunodeficiency | 2011 |