chenodeoxycholic acid has been researched along with Inborn Errors of Metabolism in 10 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (10.00) | 18.7374 |
| 1990's | 3 (30.00) | 18.2507 |
| 2000's | 1 (10.00) | 29.6817 |
| 2010's | 4 (40.00) | 24.3611 |
| 2020's | 1 (10.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ravindranath, A; Sen Sarma, M; Yachha, SK | 1 |
| Dale, RC; Mohammad, SS; Paget, SP | 1 |
| Clayton, PT; Coupry, I; Crick, PJ; Dai, D; Footitt, E; Gissen, P; Goizet, C; Griffiths, WJ; Kimura, A; Lavie, J; McClean, P; Mills, PB; Mizuochi, T; Mochel, F; Nittono, H; Schwarz, K; Stahlschmidt, J; Wang, Y | 1 |
| Huidekoper, HH; Paulusma, CC; Vaz, FM | 1 |
| Jankowska, I; Socha, P | 1 |
| Casteels, M; Clayton, PT; Lawson, AM; Mieli-Vergani, G | 1 |
| Kai, MH; Kondo, KH; Setoguchi, T | 1 |
| Kobayashi, M; Koike, M; Kurosawa, T; Murai, T; Nittono, H; Okuda, M; Okuda, S; Sakiyama, M; Takei, H; Tanaka, T; Unno, A; Yoshimura, T | 1 |
| Mosbach, EH; Salen, G; Shefer, S; Zaki, FG | 1 |
| Jakobs, C; Kleijer, WJ; Schutgens, RB; Stellaard, F; Wanders, RJ | 1 |
3 review(s) available for chenodeoxycholic acid and Inborn Errors of Metabolism
| Article | Year |
|---|---|
Current therapies and therapeutic decision making for childhood-onset movement disorders.
Topics: Adrenergic alpha-Agonists; Anticonvulsants; Autoimmune Diseases of the Nervous System; Botulinum Toxins, Type A; Cannabinoids; Cell- and Tissue-Based Therapy; Chelating Agents; Chenodeoxycholic Acid; Child; Clinical Decision-Making; Deep Brain Stimulation; Diet Therapy; Dietary Supplements; Dopamine Agents; Enzyme Replacement Therapy; GABA Agents; Gastrointestinal Agents; Genetic Therapy; Glucocorticoids; Humans; Immunoglobulins, Intravenous; Immunologic Factors; Metabolism, Inborn Errors; Monoamine Oxidase Inhibitors; Movement Disorders; Neuromuscular Agents; Organophosphorus Compounds; Pterins | 2019 |
[Delta 4-3-oxosteroid 5 beta-reductase deficiency].
Topics: Bile Acids and Salts; Biomarkers; Chenodeoxycholic Acid; Cholagogues and Choleretics; Cholic Acid; Cholic Acids; Diagnosis, Differential; Humans; Infant, Newborn; Metabolism, Inborn Errors; Oxidoreductases; Prognosis; Ursodeoxycholic Acid | 1998 |
Inborn errors of bile acid synthesis.
Topics: Animals; Bile Acids and Salts; Bile Ducts, Intrahepatic; Chemical Phenomena; Chemistry; Chenodeoxycholic Acid; Cholestasis; Cholic Acids; Humans; Liver; Metabolism, Inborn Errors; Xanthomatosis | 1977 |
7 other study(ies) available for chenodeoxycholic acid and Inborn Errors of Metabolism
| Article | Year |
|---|---|
Bile acid synthetic defects: Simplified approach in a nutshell.
Topics: Bile Acids and Salts; Chenodeoxycholic Acid; Cholesterol; Cholic Acid; Enzymes; Humans; Liver Diseases; Metabolism, Inborn Errors | 2020 |
Liver disease in infancy caused by oxysterol 7 α-hydroxylase deficiency: successful treatment with chenodeoxycholic acid.
Topics: Bile Acids and Salts; Chenodeoxycholic Acid; Consanguinity; Cytochrome P450 Family 7; Humans; Infant; Liver; Liver Diseases; Male; Metabolism, Inborn Errors; Steroid Hydroxylases | 2014 |
Extended Abstract: Deficiency of Sodium Taurocholate Cotransporting Polypeptide (SLC10A1): A New Inborn Error of Metabolism with an Attenuated Phenotype.
Topics: Chenodeoxycholic Acid; Child, Preschool; Female; Follow-Up Studies; Humans; Metabolism, Inborn Errors; Organic Anion Transporters, Sodium-Dependent; Phenotype; Symporters; Time Factors | 2017 |
Progressive familial intrahepatic cholestasis and inborn errors of bile acid synthesis.
Topics: Avitaminosis; Bile Acids and Salts; Chenodeoxycholic Acid; Child; Cholestasis, Intrahepatic; Cholic Acid; Digestive System Surgical Procedures; gamma-Glutamyltransferase; Gastrointestinal Agents; Growth Disorders; Hepatomegaly; Humans; Jaundice; Metabolism, Inborn Errors; Pruritus; Splenomegaly; Transaminases | 2012 |
Familial giant cell hepatitis with low bile acid concentrations and increased urinary excretion of specific bile alcohols: a new inborn error of bile acid synthesis?
Topics: Bile Acids and Salts; Chenodeoxycholic Acid; Cholestanols; Cholestasis; Cholic Acid; Cholic Acids; Follow-Up Studies; Giant Cells; Hepatitis; Humans; Infant; Male; Metabolism, Inborn Errors; Molecular Structure | 1995 |
3beta-hydroxy-delta5-C27-steroid dehydrogenase/isomerase deficiency in a 23-year-old woman.
Topics: 3-Hydroxysteroid Dehydrogenases; Adult; Chenodeoxycholic Acid; Cholic Acid; Female; Humans; Liver; Liver Cirrhosis; Metabolism, Inborn Errors; Steroid Isomerases; Ursodeoxycholic Acid; Vitamin K Deficiency | 2000 |
Bile acids in amniotic fluid: promising metabolites for the prenatal diagnosis of peroxisomal disorders.
Topics: Amniotic Fluid; Bile Acids and Salts; Chenodeoxycholic Acid; Cholestanols; Cholic Acids; Female; Fetus; Humans; Metabolism, Inborn Errors; Microbodies; Pregnancy; Prenatal Diagnosis | 1991 |