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Pediatrics|March 12, 2008
Amino acid cerebrospinal fluid/plasma ratios in children: influence of age, gender, and antiepileptic medicationSabine Scholl-Bürgi, Edda Haberlandt, Peter Heinz-Erian, et al.Orphanet Journal of Rare Diseases|January 6, 2012
Gastric lactobezoar - a rare disorder?Peter Heinz-Erian, Ingmar Gassner, Andreas Klein-Franke, et al.Human Genetics|April 20, 2020
AP1S1 missense mutations cause a congenital enteropathy via an epithelial barrier defectKatharina M C Klee, Andreas R Janecke, Hasret A Civan, et al.Amino Acids|October 2, 2009
Changes in plasma amino acid concentrations with increasing age in patients with propionic acidemiaSabine Scholl-Bürgi, Jörn Oliver Sass, Peter Heinz-Erian, et al.Orphanet Journal of Rare Diseases|December 20, 2013
Genotype-dependency of butyrate efficacy in children with congenital chloride diarrheaRoberto Berni Canani, Gianluca Terrin, Ausilia Elce, et al.Journal of Hepatology|April 24, 2007
Re-evaluation of the penicillamine challenge test in the diagnosis of Wilson's disease in childrenThomas Müller, Smita Koppikar, Rachel M Taylor, et al.Journal of Pediatric Gastroenterology and Nutrition|June 23, 2011
Significance of molecular testing for congenital chloride diarrheaSilvia Lechner, Frank M Ruemmele, Andreas Zankl, et al.Human Molecular Genetics|November 17, 2018
SPINT2 (HAI-2) missense variants identified in congenital sodium diarrhea/tufting enteropathy affect the ability of HAI-2 to inhibit prostasin but not matriptaseLasse Holt-Danborg, Julia Vodopiutz, Annika W Nonboe, et al.Gut|May 22, 2015
Congenital secretory diarrhoea caused by activating germline mutations in GUCY2CThomas Müller, Insha Rasool, Peter Heinz-Erian, et al.Hepatology (Baltimore, Md.)|April 2, 2004
Immunohistochemical analysis of Mallory bodies in Wilsonian and non-Wilsonian hepatic copper toxicosisThomas Müller, Cord Langner, Andrea Fuchsbichler, et al.Pageof 3