Oral cholic acid for hereditary defects of primary bile acid synthesis: a safe and effective long-term therapy.
about
Neonatal Cholestasis - Differential Diagnoses, Current Diagnostic Procedures, and TreatmentFarnesoid X receptor agonists attenuate colonic epithelial secretory function and prevent experimental diarrhoea in vivoProgressive familial intrahepatic cholestasis.Treatment of bile acid amidation defects with glycocholic acid.Primary ∆4-3-oxosteroid 5β-reductase deficiency: two cases in ChinaHomozygosity mapping identifies a bile acid biosynthetic defect in an adult with cirrhosis of unknown etiology.ACOX2 deficiency: A disorder of bile acid synthesis with transaminase elevation, liver fibrosis, ataxia, and cognitive impairment.Cholic acid therapy in Zellweger spectrum disorders.Disorders of bile acid synthesis.Acute liver failure in neonates, infants and children.Novel Mutations in the 3β-hydroxy-∆5-C27-steroid Dehydrogenase Gene (HSD3B7) in a Patient with Neonatal Cholestasis.MYO5B mutations cause cholestasis with normal serum gamma-glutamyl transferase activity in children without microvillous inclusion disease.Analysis of factors affecting the prognosis of neonatal cholestasisOral Cholic Acid Is Efficacious and Well Tolerated in Patients With Bile Acid Synthesis and Zellweger Spectrum DisordersAtypical clinical presentation and successful treatment with oral cholic acid of a child with defective bile acid synthesis due to a novel mutation in the HSD3B7 geneMolecular genetic and bile acid profiles in two Japanese patients with 3beta-hydroxy-DELTA5-C27-steroid dehydrogenase/isomerase deficiency.Growth and development of a new subspecialty: pediatric hepatology.Two neonatal cholestasis patients with mutations in the SRD5B1 (AKR1D1) gene: diagnosis and bile acid profiles during chenodeoxycholic acid treatment.Infant cholestasis patient with a novel missense mutation in the gene successfully treated by early adequate supplementation with chenodeoxycholic acid: A case report and review of the literatureThe gut microbiota drives the impact of bile acids and fat source in diet on mouse metabolismDistinguishing primary from secondary Δ(4) -3-oxosteroid 5β-reductase (SRD5B1, AKR1D1) deficiency by urinary steroid analysis
P2860
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P2860
Oral cholic acid for hereditary defects of primary bile acid synthesis: a safe and effective long-term therapy.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年学术文章
@wuu
2009年学术文章
@zh
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
2009年學術文章
@zh-hant
name
Oral cholic acid for hereditar ...... d effective long-term therapy.
@en
Oral cholic acid for hereditar ...... d effective long-term therapy.
@nl
type
label
Oral cholic acid for hereditar ...... d effective long-term therapy.
@en
Oral cholic acid for hereditar ...... d effective long-term therapy.
@nl
prefLabel
Oral cholic acid for hereditar ...... d effective long-term therapy.
@en
Oral cholic acid for hereditar ...... d effective long-term therapy.
@nl
P2093
P1433
P1476
Oral cholic acid for hereditar ...... d effective long-term therapy.
@en
P2093
Anne Davit-Spraul
Emmanuel Gonzales
Isabelle Vincent
James E Heubi
Kenneth D R Setchell
Marie F Gerhardt
Monique Fabre
Olivier Bernard
P304
1310-1320.e1-3
P356
10.1053/J.GASTRO.2009.07.043
P407
P577
2009-07-19T00:00:00Z