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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 28, 2012
[Esophageal atresia]F Gottrand, R Sfeir, C Thumerelle, et al.
Clinical Genetics|April 19, 2011
Whole-genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotypeG D'Amours, Z Kibar, G Mathonnet, et al.
Annales Francaises D'Anesthesie Et De Reanimation|January 1, 1985
[Acute renal failure after extracorporeal circulation with aortic counterpulsation in surgically treated patients]Y Blanloeil, M Train, C Vincent, et al.
Journal of Pediatric Gastroenterology and Nutrition|March 6, 1999
Nitrous oxide sedation in pediatric patients undergoing gastrointestinal endoscopyL Michaud, F Gottrand, P S Ganga-Zandzou, et al.
BMJ Open|June 29, 2022
Scoping review of costs of implementation strategies in community, public health and healthcare settingsTzeyu L Michaud, Emiliane Pereira, Gwenndolyn Porter, et al.
Journal of Physical Activity & Health|August 7, 2019
The Association of Physical Activity and Mortality Risk Reduction Among Smokers: Results From 1998-2009 National Health Interview Surveys-National Death Index LinkageMohammad Siahpush, Trish D Levan, Minh N Nguyen, et al.
American Journal of Medical Genetics. Part A|April 23, 2017
Expansion of the clinical phenotype of the distal 10q26.3 deletion syndrome to include ataxia and hyperemia of the hands and feetMelanie Lacaria, Myriam Srour, Jacques L Michaud, et al.
Chirurgie; Memoires De L'Academie De Chirurgie|January 1, 1993
[Multiple and recurrent cardiac myxomas. Is it a familial disease?]D Duveau, O Baron, B Jegou, et al.
Journal of Health Economics and Outcomes Research|November 24, 2025
Quantifying the Public Health Impact of Lyme Disease in Minnesota: A Simulation Analysis of Reported and Unreported CasesKathleen E Angell, M Jana Broadhurst, Jianghu J Dong, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|June 15, 2021
Differential auditory brain response abnormalities in two intellectual disability conditions: SYNGAP1 mutations and Down syndromeValérie Côté, Inga S Knoth, Kristian Agbogba, et al.
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