| scholarly article | Q13442814 |
| review article | Q7318358 |
| P356 | DOI | 10.1016/S1089-3261(05)70144-6 |
| P698 | PubMed publication ID | 11232360 |
| P2093 | author name string | K E Bove | |
| P2860 | cites work | Identification of a new inborn error in bile acid synthesis: mutation of the oxysterol 7alpha-hydroxylase gene causes severe neonatal liver disease | Q24564340 |
| Familial giant cell hepatitis associated with synthesis of 3 beta, 7 alpha-dihydroxy-and 3 beta,7 alpha, 12 alpha-trihydroxy-5-cholenoic acids | Q28361624 | ||
| Inborn errors of bile acid biosynthesis and transport. Novel forms of metabolic liver disease | Q33591444 | ||
| Genetic basis of progressive familial intrahepatic cholestasis | Q33715915 | ||
| Bile acid synthetic defects and liver disease | Q33792325 | ||
| Treatment of chronic liver disease caused by 3 beta-hydroxy-delta 5-C27-steroid dehydrogenase deficiency with chenodeoxycholic acid | Q35625222 | ||
| Disruption of cholesterol 7alpha-hydroxylase gene in mice. II. Bile acid deficiency is overcome by induction of oxysterol 7alpha-hydroxylase. | Q35671417 | ||
| Bile acid biosynthesis | Q36136767 | ||
| Infantile liver giant cells: immunohistological study of their proliferative state and possible mechanisms of formation | Q38468420 | ||
| Lack of 3 beta-hydroxy-delta 5-C27-steroid dehydrogenase/isomerase in fibroblasts from a child with urinary excretion of 3 beta-hydroxy-delta 5-bile acids. A new inborn error of metabolism | Q40511951 | ||
| Disturbances in bile acid metabolism of infants with the Zellweger (cerebro-hepato-renal) syndrome | Q41642567 | ||
| Quantitative estimations of the contribution of different bile acid pathways to total bile acid synthesis in the rat. | Q45108263 | ||
| 3 beta-hydroxy-delta 5-C27-steroid dehydrogenase deficiency; effect of chenodeoxycholic acid therapy on liver histology | Q45244783 | ||
| A new category of causes of intrahepatic cholestasis. | Q45904712 | ||
| Inborn errors of bile acid synthesis. | Q64930478 | ||
| Oral bile acid treatment and the patient with zellweger syndrome | Q67743311 | ||
| 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? | Q71835309 | ||
| Delta 4-3-oxosteroid 5 beta-reductase deficiency causing neonatal liver failure and hemochromatosis | Q72757062 | ||
| Measurement of peroxisomal fatty acid beta-oxidation in cultured human skin fibroblasts | Q73117534 | ||
| Differential interaction of bile acids from patients with inborn errors of bile acid synthesis with hepatocellular bile acid transporters | Q73138562 | ||
| Abnormal bile acid metabolism and neonatal hemochromatosis: a subset with poor prognosis | Q73669851 | ||
| P433 | issue | 4 | |
| P921 | main subject | liver disease | Q929737 |
| P304 | page(s) | 831-848 | |
| P577 | publication date | 2000-11-01 | |
| P1433 | published in | Clinics in liver disease | Q26842322 |
| P1476 | title | Liver disease caused by disorders of bile acid synthesis | |
| P478 | volume | 4 |
| Q24302579 | A novel bile acid biosynthesis defect due to a deficiency of peroxisomal ABCD3 |
| Q34746201 | Common diagnostic problems in pediatric liver pathology |
| Q34303156 | Neonatal hepatitis syndrome |
| Q53614633 | Nonobstructive neonatal cholestasis: clinical outcome and scoring of the histopathological changes in liver biopsies. |
| Q34579067 | Update on the etiologies and management of neonatal cholestasis |
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