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[The first consultation with an adolescent].
Stheneur C, Alvin P, Boudaillez B, Gronnier P, Jacquin P, Picherot G, Renondeau JY, Salinier C, de Tournemire R, Lemerle S; les membres de la Com'ado de la Société française de pédiatrie. Stheneur C, et al. Arch Pediatr. 2009 Sep;16(9):1309-12. doi: 10.1016/j.arcped.2009.06.003. Epub 2009 Jul 14. Arch Pediatr. 2009. PMID: 19604679 French.
Depressive symptoms among teenagers in the emergency department: prevalence estimate and concordance with parental perceptions.
Sznajder M, Speranza M, Guyot C, Martin S, Nathanson S, Kerbourc'h S, Biscardi S, Cottinet SL, Delalande D, Chevallier B, Revah-Levy A, Ghout I, Stheneur C. Sznajder M, et al. Among authors: stheneur c. Eur J Pediatr. 2013 Dec;172(12):1587-96. doi: 10.1007/s00431-013-2060-1. Epub 2013 Jul 12. Eur J Pediatr. 2013. PMID: 23846194
[Perception of adolescent medicine among French pediatric residents].
Ibrahim N, de Tournemire R, Jacquin P, Stheneur C, Boudailliez B. Ibrahim N, et al. Among authors: stheneur c. Arch Pediatr. 2016 Jul;23(7):695-705. doi: 10.1016/j.arcped.2016.04.002. Epub 2016 Jun 1. Arch Pediatr. 2016. PMID: 27262627 French.
Checklist for follow-up of adolescents with chronic illness. A monitoring tool to help prepare the transition from pediatric to adult care.
Fourmaux C, Lefevre H, Safsaf H, Jacquin P, Rouget S, de Tournemire R, Lambert AS, Devernay M, Carlier-Gonot A, Marin M, Stheneur C; French Society for Adolescent Health. Fourmaux C, et al. Among authors: stheneur c. Arch Pediatr. 2021 Aug;28(6):480-484. doi: 10.1016/j.arcped.2021.04.013. Epub 2021 Jun 17. Arch Pediatr. 2021. PMID: 34147297 Free article. Review.
Recovery Trajectories in Adolescent Girls with Anorexia Nervosa.
Bédard A, Bernard C, Meilleur D, Taddeo D, Pesant C, Di Meglio G, Gingras N, Thibault I, Agostino H, Bélanger R, Nadeau PO, Frappier JY, Stheneur C, Dufresne L, Bégin C. Bédard A, et al. Among authors: stheneur c. J Clin Med. 2024 Jan 29;13(3):778. doi: 10.3390/jcm13030778. J Clin Med. 2024. PMID: 38337472 Free PMC article.
Clinical and molecular study of 320 children with Marfan syndrome and related type I fibrillinopathies in a series of 1009 probands with pathogenic FBN1 mutations.
Faivre L, Masurel-Paulet A, Collod-Béroud G, Callewaert BL, Child AH, Stheneur C, Binquet C, Gautier E, Chevallier B, Huet F, Loeys BL, Arbustini E, Mayer K, Arslan-Kirchner M, Kiotsekoglou A, Comeglio P, Grasso M, Halliday DJ, Béroud C, Bonithon-Kopp C, Claustres M, Robinson PN, Adès L, De Backer J, Coucke P, Francke U, De Paepe A, Boileau C, Jondeau G. Faivre L, et al. Among authors: stheneur c. Pediatrics. 2009 Jan;123(1):391-8. doi: 10.1542/peds.2008-0703. Pediatrics. 2009. PMID: 19117906 Free article.
77 results