Stéphanie Marotte

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BACKGROUND Metabolic bone disease is common in children receiving home parenteral nutrition (HPN) for intestinal failure (IF). Long-term evolution of bone mass in pediatric IF is poorly documented. The aims of this study were (1) to determine the prevalence of low bone mass (LBM) in children receiving HPN for IF, (2) to evaluate the evolution of total bone(More)
To the Editor: Wilson’s disease (WD) is an autosomal recessive disease caused by mutations in the ATP7B gene, resulting in accumulation of copper in various organs including liver, cornea, and brain [1]. AADSL and EASL Guidelines have been published to help physicians in diagnosis and treatment [2,3]. We report diagnosis of WD in a 43-year-old asymptomatic(More)
BACKGROUND & AIMS This retrospective study evaluated the impact of new organization during the moving to a new university pediatric hospital on the incidence of central catheter-related blood stream infections (CRBSIs) among children on long-term parenteral nutrition. METHODS The study ran from April 2007 to March 2014, starting a year prior to(More)
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