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Annals of Surgical Oncology|June 4, 2014
Genomic profiling of intrahepatic cholangiocarcinoma: refining prognosis and identifying therapeutic targetsAndrew X Zhu, Darrell R Borger, Yuhree Kim, et al.Human Mutation|November 22, 2008
Genomic deletions of OFD1 account for 23% of oral-facial-digital type 1 syndrome after negative DNA sequencingChristel Thauvin-Robinet, Brunella Franco, Pascale Saugier-Veber, et al.European Journal of Human Genetics : EJHG|October 16, 2014
Autosomal-recessive SASH1 variants associated with a new genodermatosis with pigmentation defects, palmoplantar keratoderma and skin carcinomaJean-Benoît Courcet, Siham Chafai Elalaoui, Laurence Duplomb, et al.European Journal of Medical Genetics|March 26, 2013
Detailed clinical, genetic and neuroimaging characterization of OFD VI syndromeVéronique Darmency-Stamboul, Lydie Burglen, Estelle Lopez, et al.American Journal of Medical Genetics. Part A|September 20, 2015
Compound heterozygous PKHD1 variants cause a wide spectrum of ductal plate malformationsJean-Benoît Courcet, Anne Minello, Fabienne Prieur, et al.Journal of the National Cancer Institute|September 20, 2017
Comprehensive Intrametastatic Immune Quantification and Major Impact of Immunoscore on SurvivalBernhard Mlecnik, Marc Van den Eynde, Gabriela Bindea, et al.Antioxidants & Redox Signaling|February 15, 2022
Evidence for Constitutive Microbiota-Dependent Short-Term Control of Food Intake in Mice: Is There a Link with Inflammation, Oxidative Stress, Endotoxemia, and GLP-1?Selma Ben Fradj, Emmanuelle Nédélec, Juliette Salvi, et al.Journal of Visceral Surgery|May 14, 2013
Is port-site resection necessary in the surgical management of gallbladder cancer?D Fuks, J-M Regimbeau, P Pessaux, et al.Endoscopy|April 4, 2019
Endoscopic management of common bile duct stones: European Society of Gastrointestinal Endoscopy (ESGE) guidelineGianpiero Manes, Gregorios Paspatis, Lars Aabakken, et al.Clinical Genetics|October 13, 2009
Renal insufficiency, a frequent complication with age in oral-facial-digital syndrome type IS Saal, L Faivre, Bernard Aral, et al.Pageof 26