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chenodeoxycholic acid and Metabolism, Inborn Errors

chenodeoxycholic acid has been researched along with Metabolism, Inborn Errors in 10 studies

Research

Studies (10)

TimeframeStudies, this research(%)All Research%
pre-19901 (10.00)18.7374
1990's3 (30.00)18.2507
2000's1 (10.00)29.6817
2010's4 (40.00)24.3611
2020's1 (10.00)2.80

Authors

AuthorsStudies
Ravindranath, A; Sen Sarma, M; Yachha, SK1
Dale, RC; Mohammad, SS; Paget, SP1
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, Y1
Huidekoper, HH; Paulusma, CC; Vaz, FM1
Jankowska, I; Socha, P1
Casteels, M; Clayton, PT; Lawson, AM; Mieli-Vergani, G1
Kai, MH; Kondo, KH; Setoguchi, T1
Kobayashi, M; Koike, M; Kurosawa, T; Murai, T; Nittono, H; Okuda, M; Okuda, S; Sakiyama, M; Takei, H; Tanaka, T; Unno, A; Yoshimura, T1
Mosbach, EH; Salen, G; Shefer, S; Zaki, FG1
Jakobs, C; Kleijer, WJ; Schutgens, RB; Stellaard, F; Wanders, RJ1

Reviews

3 review(s) available for chenodeoxycholic acid and Metabolism, Inborn Errors

ArticleYear
Current therapies and therapeutic decision making for childhood-onset movement disorders.
    Movement disorders : official journal of the Movement Disorder Society, 2019, Volume: 34, Issue:5

    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].
    Ryoikibetsu shokogun shirizu, 1998, Issue:19 Pt 2

    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.
    Clinics in gastroenterology, 1977, Volume: 6, Issue:1

    Topics: Animals; Bile Acids and Salts; Bile Ducts, Intrahepatic; Chemical Phenomena; Chemistry; Chenodeoxycholic Acid; Cholestasis; Cholic Acids; Humans; Liver; Metabolism, Inborn Errors; Xanthomatosis

1977

Other Studies

7 other study(ies) available for chenodeoxycholic acid and Metabolism, Inborn Errors

ArticleYear
Bile acid synthetic defects: Simplified approach in a nutshell.
    Hepatobiliary & pancreatic diseases international : HBPD INT, 2020, Volume: 19, Issue:1

    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.
    Journal of inherited metabolic disease, 2014, Volume: 37, Issue:5

    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.
    Digestive diseases (Basel, Switzerland), 2017, Volume: 35, Issue:3

    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.
    Clinics and research in hepatology and gastroenterology, 2012, Volume: 36, Issue:3

    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?
    Pediatric research, 1995, Volume: 37, Issue:4 Pt 1

    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.
    Pediatrics international : official journal of the Japan Pediatric Society, 2000, Volume: 42, Issue:6

    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.
    Journal of inherited metabolic disease, 1991, Volume: 14, Issue:3

    Topics: Amniotic Fluid; Bile Acids and Salts; Chenodeoxycholic Acid; Cholestanols; Cholic Acids; Female; Fetus; Humans; Metabolism, Inborn Errors; Microbodies; Pregnancy; Prenatal Diagnosis

1991