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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 6, 2005
[Fatal neonatal respiratory distress in Niemann-Pick C2 and prenatal diagnosis with mutations in gene HE1/NPC2]C Morisot, G Millat, A Coeslier, et al.Gut|February 16, 2005
Environmental risk factors in paediatric inflammatory bowel diseases: a population based case control studyS Baron, D Turck, C Leplat, et al.Pediatric Obesity|December 18, 2014
Liver enzymes and clustering cardiometabolic risk factors in European adolescents: the HELENA studyI Labayen, J R Ruiz, F B Ortega, et al.International Journal of Obesity (2005)|November 26, 2008
Socioeconomic questionnaire and clinical assessment in the HELENA Cross-Sectional Study: methodologyC Iliescu, L Béghin, L Maes, et al.European Journal of Nutrition|November 30, 2016
Dietary sources of sugars in adolescents' diet: the HELENA studyM I Mesana, A Hilbig, O Androutsos, et al.Cardiology in the Young|April 6, 2012
Risk of congenital heart defects is influenced by genetic variation in folate metabolismKaren E Christensen, Yassamin Feroz Zada, Charles V Rohlicek, et al.Human Genetics|December 22, 1999
Alström syndrome: further evidence for linkage to human chromosome 2p13G B Collin, J D Marshall, C F Boerkoel, et al.Eneuro|April 18, 2023
Syngap1 Disruption Induced by Recombination between Inverted loxP Sites Is Associated with Hippocampal Interneuron DysfunctionAbdessattar Khlaifia, Vidya Jadhav, Marc Danik, et al.Journal of the American Heart Association|November 26, 2025
Association Between Monoclonal Gammopathy of Undetermined Significance and Cardiovascular Disease Risk: A Veterans Health Administration StudyTzeyu L Michaud, Mei Wang, Daphne R Friedman, et al.Clinical Genetics|May 2, 2015
A homozygous mutation in SLC1A4 in siblings with severe intellectual disability and microcephalyM Srour, F F Hamdan, Z Gan-Or, et al.Pageof 61