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Journal of Lipid Research|December 20, 1999
Phenotypic characterization of lith genes that determine susceptibility to cholesterol cholelithiasis in inbred mice. Pathophysiology Of biliary lipid secretionD Q Wang, F Lammert, B Paigen, et al.
QJM : Monthly Journal of the Association of Physicians|March 7, 2019
Medication adherence among patients with chronic diseases: a survey-based study in pharmaciesC Jüngst, S Gräber, S Simons, et al.
Zeitschrift Fur Gastroenterologie|January 12, 2008
[Recurrent intrahepatic cholestasis of pregnancy and chain-like choledocholithiasis in a female patient with stop codon in the ABDC4-gene of the hepatobiliary phospholipid transporter]K Muehlenberg, K Wiedmann, H Keppeler, et al.
Zeitschrift Fur Gastroenterologie|February 9, 2016
[Prevalence and risk factors of drug induced liver disease: a survey based study in pharmacies]C Jüngst, S Gräber, D Klahn, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|December 6, 2005
Eosinophilic gastroenteritis with severe protein-losing enteropathy: successful treatment with budesonideE Siewert, F Lammert, P Koppitz, et al.
Journal of Lipid Research|March 5, 1999
No pathophysiologic relationship of soluble biliary proteins to cholesterol crystallization in human bileD Q Wang, D E Cohen, F Lammert, et al.
European Journal of Medical Research|April 22, 2009
Coinheritance of hereditary spherocytosis and reversibility of cirrhosis in a young female patient with hereditary hemochromatosisA Höblinger, C Erdmann, C P Strassburg, et al.
Zeitschrift Fur Gastroenterologie|May 12, 2006
Portal hypertension and nodular regenerative hyperplasia in a patient with celiac diseaseE Biecker, J Trebicka, H-P Fischer, et al.
Colorectal Disease : the Official Journal of the Association of Coloproctology of Great Britain and Ireland|April 4, 2012
MUTYH hotspot mutations in unselected colonoscopy patientsM Casper, G Plotz, B Juengling, et al.
Journal of Internal Medicine|April 17, 2015
A genetic variant in the promoter of phosphate-activated glutaminase is associated with hepatic encephalopathyL B Mayer, M Krawczyk, F Grünhage, et al.
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