Thompson R - Search Results

1

Donor transmitted mutation of the ABCB11 gene and ensuing intrahepatic cholestasis of pregnancy in a liver transplant recipient.

Lim TY, Coltart I, Foskett P, Thompson R, Strautnieks S, Penna L, Williamson C, Miquel R, Heneghan MA. Lim TY, et al. Among authors: thompson r. Liver Transpl. 2017 Sep;23(9):1229-1232. doi: 10.1002/lt.24776. Liver Transpl. 2017. PMID: 28524363 No abstract available.

2

Inherited disorders of transport in the liver.

Thompson R, Strautnieks S. Thompson R, et al. Curr Opin Genet Dev. 2000 Jun;10(3):310-3. doi: 10.1016/s0959-437x(00)00078-2. Curr Opin Genet Dev. 2000. PMID: 10826986 Review.

3

BSEP: function and role in progressive familial intrahepatic cholestasis.

Thompson R, Strautnieks S. Thompson R, et al. Semin Liver Dis. 2001 Nov;21(4):545-50. doi: 10.1055/s-2001-19038. Semin Liver Dis. 2001. PMID: 11745042 Review.

4

The human bile salt export pump: characterization of substrate specificity and identification of inhibitors.

Byrne JA, Strautnieks SS, Mieli-Vergani G, Higgins CF, Linton KJ, Thompson RJ. Byrne JA, et al. Gastroenterology. 2002 Nov;123(5):1649-58. doi: 10.1053/gast.2002.36591. Gastroenterology. 2002. PMID: 12404239

5

Progressive familial intrahepatic cholestasis, type 1, is associated with decreased farnesoid X receptor activity.

Chen F, Ananthanarayanan M, Emre S, Neimark E, Bull LN, Knisely AS, Strautnieks SS, Thompson RJ, Magid MS, Gordon R, Balasubramanian N, Suchy FJ, Shneider BL. Chen F, et al. Among authors: thompson rj. Gastroenterology. 2004 Mar;126(3):756-64. doi: 10.1053/j.gastro.2003.12.013. Gastroenterology. 2004. PMID: 14988830

6

VPS33B mutation with ichthyosis, cholestasis, and renal dysfunction but without arthrogryposis: incomplete ARC syndrome phenotype.

Bull LN, Mahmoodi V, Baker AJ, Jones R, Strautnieks SS, Thompson RJ, Knisely AS. Bull LN, et al. Among authors: thompson rj. J Pediatr. 2006 Feb;148(2):269-71. doi: 10.1016/j.jpeds.2005.10.005. J Pediatr. 2006. PMID: 16492441

7

Exocrine pancreatic function in children with progressive familial intrahepatic cholestasis type 2.

Walkowiak J, Jankowska I, Pawlowska J, Strautnieks S, Bull L, Thompson R, Herzig KH, Socha J. Walkowiak J, et al. Among authors: thompson r. J Pediatr Gastroenterol Nutr. 2006 Apr;42(4):416-8. doi: 10.1097/01.mpg.0000218154.26792.6a. J Pediatr Gastroenterol Nutr. 2006. PMID: 16641580

8

Hepatocellular carcinoma in ten children under five years of age with bile salt export pump deficiency.

Knisely AS, Strautnieks SS, Meier Y, Stieger B, Byrne JA, Portmann BC, Bull LN, Pawlikowska L, Bilezikçi B, Ozçay F, László A, Tiszlavicz L, Moore L, Raftos J, Arnell H, Fischler B, Németh A, Papadogiannakis N, Cielecka-Kuszyk J, Jankowska I, Pawłowska J, Melín-Aldana H, Emerick KM, Whitington PF, Mieli-Vergani G, Thompson RJ. Knisely AS, et al. Hepatology. 2006 Aug;44(2):478-86. doi: 10.1002/hep.21287. Hepatology. 2006. PMID: 16871584

9

Severe bile salt export pump deficiency: 82 different ABCB11 mutations in 109 families.

Strautnieks SS, Byrne JA, Pawlikowska L, Cebecauerová D, Rayner A, Dutton L, Meier Y, Antoniou A, Stieger B, Arnell H, Ozçay F, Al-Hussaini HF, Bassas AF, Verkade HJ, Fischler B, Németh A, Kotalová R, Shneider BL, Cielecka-Kuszyk J, McClean P, Whitington PF, Sokal E, Jirsa M, Wali SH, Jankowska I, Pawłowska J, Mieli-Vergani G, Knisely AS, Bull LN, Thompson RJ. Strautnieks SS, et al. Among authors: thompson rj. Gastroenterology. 2008 Apr;134(4):1203-14. doi: 10.1053/j.gastro.2008.01.038. Epub 2008 Jan 18. Gastroenterology. 2008. PMID: 18395098 Free article.

10

Congenital bile duct anomalies (biliary atresia) and chromosome 22 aneuploidy.

Allotey J, Lacaille F, Lees MM, Strautnieks S, Thompson RJ, Davenport M. Allotey J, et al. J Pediatr Surg. 2008 Sep;43(9):1736-40. doi: 10.1016/j.jpedsurg.2008.05.012. J Pediatr Surg. 2008. PMID: 18779018

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