chenodeoxycholic acid has been researched along with Infant, Newborn, Diseases in 2 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 | 2 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Hashimoto, T; Kimura, A; Kurosawa, T; Matsuishi, T; Mizuochi, T; Nittono, H; Seki, Y; Takahashi, T; Takao, A; Takei, H; Ueki, I | 1 |
| Hasegawa, T; Hayashi, S; Homma, K; Hoshina, T; Ihara, K; Kimura, A; Kurosawa, T; Matsuishi, T; Mizuochi, T; Morimura, T; Nittono, H; Ohno, Y; Ohtake, A; Seki, Y; Takahashi, T; Takei, H | 1 |
2 other study(ies) available for chenodeoxycholic acid and Infant, Newborn, Diseases
| Article | Year |
|---|---|
Molecular genetic and bile acid profiles in two Japanese patients with 3beta-hydroxy-DELTA5-C27-steroid dehydrogenase/isomerase deficiency.
Topics: 3-Hydroxysteroid Dehydrogenases; Base Sequence; Bile Acids and Salts; Chenodeoxycholic Acid; Cholestasis; DNA Primers; Gas Chromatography-Mass Spectrometry; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Japan; Liver; Male; Molecular Sequence Data; Mutation; Sequence Analysis, DNA | 2010 |
Two neonatal cholestasis patients with mutations in the SRD5B1 (AKR1D1) gene: diagnosis and bile acid profiles during chenodeoxycholic acid treatment.
Topics: Asian People; Bile Acids and Salts; Chenodeoxycholic Acid; Cholestasis; Female; Gastrointestinal Agents; Humans; Infant, Newborn; Infant, Newborn, Diseases; Liver; Male; Mutation; Oxidoreductases | 2013 |