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The FEBS Journal|December 13, 2005
Identification of the epitope of a monoclonal antibody that disrupts binding of human transferrin to the human transferrin receptorEvelyn M Teh, Jeff Hewitt, Karen C Ung, et al.Gut|April 29, 2009
Polymorphisms in E-cadherin (CDH1) result in a mis-localised cytoplasmic protein that is associated with Crohn's diseaseA M Muise, T D Walters, W K Glowacka, et al.Hepatology (Baltimore, Md.)|November 1, 1995
Primary sclerosing cholangitis in 32 children: clinical, laboratory, and radiographic features, with survival analysisM Wilschanski, P Chait, J A Wade, et al.Journal of Pediatric Gastroenterology and Nutrition|February 1, 1992
Relationship of common laboratory parameters to the activity of Crohn's disease in childrenJ S Hyams, F Mandel, G D Ferry, et al.American Journal of Physiology. Gastrointestinal and Liver Physiology|December 19, 2009
Human hephaestin expression is not limited to enterocytes of the gastrointestinal tract but is also found in the antrum, the enteric nervous system, and pancreatic {beta}-cellsDavid M Hudson, Susan B Curtis, Valerie C Smith, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|March 23, 2011
The changing face of hepatitis in boys with haemophilia associated with increased prevalence of obesityS Revel-Vilk, P Komvilaisak, V Blanchette, et al.Gut|November 6, 2007
Severe paediatric ulcerative colitis: incidence, outcomes and optimal timing for second-line therapyD Turner, C M Walsh, E I Benchimol, et al.Journal of Pediatric Gastroenterology and Nutrition|May 1, 1991
Development and validation of a pediatric Crohn's disease activity indexJ S Hyams, G D Ferry, F S Mandel, et al.Journal of Pediatric Gastroenterology and Nutrition|July 1, 1993
Olsalazine versus sulfasalazine in mild to moderate childhood ulcerative colitis: results of the Pediatric Gastroenterology Collaborative Research Group Clinical TrialG D Ferry, B S Kirschner, R J Grand, et al.British Journal of Haematology|January 26, 2005
Severe FVII deficiency caused by a new point mutation combined with a previously undetected gene deletionJeff Hewitt, Jennifer N M Ballard, Tanya N Nelson, et al.Pageof 10