These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
30. [Intrahepatic cholestasis caused by biochemical errors of bile acids. Part I --Nosographic, pathogenetic, diagnostic features]. Lovisetto P; Raviolo P Minerva Med; 1994 Nov; 85(11):589-96. PubMed ID: 7808683 [TBL] [Abstract][Full Text] [Related]
31. [Cholestasis in total parenteral nutrition. A review]. Böhles H Infusionsther Klin Ernahr; 1987 Feb; 14 Suppl 1():3-9. PubMed ID: 3106211 [TBL] [Abstract][Full Text] [Related]
32. Genetics of familial intrahepatic cholestasis syndromes. van Mil SW; Houwen RH; Klomp LW J Med Genet; 2005 Jun; 42(6):449-63. PubMed ID: 15937079 [TBL] [Abstract][Full Text] [Related]
33. Identification of a new inborn error in bile acid synthesis: mutation of the oxysterol 7alpha-hydroxylase gene causes severe neonatal liver disease. Setchell KD; Schwarz M; O'Connell NC; Lund EG; Davis DL; Lathe R; Thompson HR; Weslie Tyson R; Sokol RJ; Russell DW J Clin Invest; 1998 Nov; 102(9):1690-703. PubMed ID: 9802883 [TBL] [Abstract][Full Text] [Related]
34. [Intrahepatic cholestasis due to biochemical errors of bile acids. II. Clinical and therapeutic aspects]. Lovisetto P; Raviolo P Minerva Med; 1994 Dec; 85(12):639-46. PubMed ID: 7854557 [TBL] [Abstract][Full Text] [Related]
35. Value of bile acid determination for the diagnosis of neonatal jaundice. Pawłowska J; Bogoniowska Z; Szczygielska-Kozak M; Wróblewska Z; Socha J Mater Med Pol; 1990; 22(2):112-7. PubMed ID: 2102973 [TBL] [Abstract][Full Text] [Related]
36. Infant cholestasis patient with a novel missense mutation in the Wang HH; Wen FQ; Dai DL; Wang JS; Zhao J; Setchell KD; Shi LN; Zhou SM; Liu SX; Yang QH World J Gastroenterol; 2018 Sep; 24(35):4086-4092. PubMed ID: 30254413 [TBL] [Abstract][Full Text] [Related]
37. Late-Onset Drug-Induced Cholestasis in a Living-Related Liver Transplant Donor With Progressive Familial Intrahepatic Cholestasis. Harmancı Ö; Ensaroğlu F; Özçay F; Öcal S; Korkmaz M; Özdemir BH; Selçuk H; Moray G; Haberal M Exp Clin Transplant; 2015 Nov; 13 Suppl 3():107-9. PubMed ID: 26640927 [TBL] [Abstract][Full Text] [Related]
38. [Transient hypoplasia of the intrahepatic bile ducts. Clinical and morphologic studies]. Sacher M; Paky F; Stögmann W; Thaler H Monatsschr Kinderheilkd; 1985 Nov; 133(11):840-2. PubMed ID: 4079946 [TBL] [Abstract][Full Text] [Related]
39. The histidine-loop is essential for transport activity of human MDR3. A novel mutation of MDR3 in a patient with progressive familial intrahepatic cholestasis type 3. Dzagania T; Engelmann G; Häussinger D; Schmitt L; Flechtenmacher C; Rtskhiladze I; Kubitz R Gene; 2012 Sep; 506(1):141-5. PubMed ID: 22766396 [TBL] [Abstract][Full Text] [Related]
40. Successful treatment of an infant with congenital bile acid synthesis disorder type 3 by ursodeoxycholic acid: a case report. Mo W; Wang F; Zhou C; Ma T; Pan Z; Xie M; Ren H; Xie Y J Med Case Rep; 2022 Apr; 16(1):139. PubMed ID: 35387662 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]