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Gastroenterology|March 5, 2002
A homozygous HFE gene splice site mutation (IVS5+1 G/A) in a hereditary hemochromatosis patient of Vietnamese originMichael Steiner, Kenneth Ocran, Janine Genschel, et al.
Journal of the American College of Cardiology|October 16, 2007
Altered intestinal function in patients with chronic heart failureAnja Sandek, Juergen Bauditz, Alexander Swidsinski, et al.
Pancreas|March 17, 2009
The role of epoxide hydrolase Y113H gene variant in pancreatic diseasesJohann Ockenga, Sebastian Strunck, Cora Post, et al.
The American Journal of Gastroenterology|February 24, 2006
DLG5 variants in inflammatory bowel diseaseCarsten Büning, Lars Geerdts, Thomas Fiedler, et al.
Clinical Nutrition (Edinburgh, Scotland)|May 16, 2006
The German hospital malnutrition studyMatthias Pirlich, Tatjana Schütz, Kristina Norman, et al.
Inflammatory Bowel Diseases|December 20, 2007
No association of the CARD8 (TUCAN) c.30T>A (p.C10X) variant with Crohn's disease: a study in 3 independent European cohortsCarsten Büning, Hartmut H-J Schmidt, Tamás Molnár, et al.
Journal of Crohn'S & Colitis|December 22, 2010
A study in three European IBD cohorts confirms that the ATG16L1 c.898A>G (p.Thr300Ala) variant is a susceptibility factor for Crohn's diseaseCarsten Büning, Tahir Durmus, Tamas Molnar, et al.
Clinical Nutrition (Edinburgh, Scotland)|August 23, 2008
Cachexia: a new definitionWilliam J Evans, John E Morley, Josep Argilés, et al.
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