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2004 2
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19 results

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Page 1
Laboratory diagnosis of hypophosphatasia.
Gennero I, Conte-Auriol F, Salles JP. Gennero I, et al. Among authors: conte auriol f. Arch Pediatr. 2017 May;24(5S2):5S57-5S60. doi: 10.1016/S0929-693X(18)30015-0. Arch Pediatr. 2017. PMID: 29405933
[Legal aspects of consent in children (Part 1)].
Nacka F, Benadjaoud L, Fayon M, Jacqz-Aigrain E; Membres du Réseau Pédiatrique Inserm des Centres d'investigations cliniques (CIC); Demarez JP. Nacka F, et al. Arch Pediatr. 2015 Sep;22(9):983-8. doi: 10.1016/j.arcped.2015.06.013. Epub 2015 Jul 27. Arch Pediatr. 2015. PMID: 26228811 Review. French.
[New molecular mechanisms of growth hormone insensitivity].
Edouard T, Raynal P, Yart A, Conte-Auriol F, Salles JP, Tauber M. Edouard T, et al. Among authors: conte auriol f. Arch Pediatr. 2008 Feb;15(2):179-88. doi: 10.1016/j.arcped.2007.10.023. Epub 2008 Jan 18. Arch Pediatr. 2008. PMID: 18207712 Review. French.
Hyperghrelinemia precedes obesity in Prader-Willi syndrome.
Feigerlová E, Diene G, Conte-Auriol F, Molinas C, Gennero I, Salles JP, Arnaud C, Tauber M. Feigerlová E, et al. Among authors: conte auriol f. J Clin Endocrinol Metab. 2008 Jul;93(7):2800-5. doi: 10.1210/jc.2007-2138. Epub 2008 May 6. J Clin Endocrinol Metab. 2008. PMID: 18460565
Bone defects in LPA receptor genetically modified mice.
Salles JP, Laurencin-Dalicieux S, Conte-Auriol F, Briand-Mésange F, Gennero I. Salles JP, et al. Among authors: conte auriol f. Biochim Biophys Acta. 2013 Jan;1831(1):93-8. doi: 10.1016/j.bbalip.2012.07.018. Epub 2012 Jul 31. Biochim Biophys Acta. 2013. PMID: 22867754
[Osteogenesis factors in childhood].
Salles JP, Gennero I, Moulin P, Conte-Auriol F, Edouard T, Tauber M. Salles JP, et al. Among authors: conte auriol f. Arch Pediatr. 2009 Jun;16(6):611-3. doi: 10.1016/S0929-693X(09)74086-2. Arch Pediatr. 2009. PMID: 19541104 French. No abstract available.
[Consent in children: Practical situations (part 2)].
Nacka F, Benadjaoud L, Fayon M, Jacqz-Aigrain E; \membres du réseau pédiatrique Inserm des centres d'investigations cliniques (CIC); Demarez JP. Nacka F, et al. Arch Pediatr. 2015 Sep;22(9):989-95. doi: 10.1016/j.arcped.2015.06.010. Epub 2015 Jul 27. Arch Pediatr. 2015. PMID: 26228807 French.
Highly restricted deletion of the SNORD116 region is implicated in Prader-Willi Syndrome.
Bieth E, Eddiry S, Gaston V, Lorenzini F, Buffet A, Conte Auriol F, Molinas C, Cailley D, Rooryck C, Arveiler B, Cavaillé J, Salles JP, Tauber M. Bieth E, et al. Among authors: conte auriol f. Eur J Hum Genet. 2015 Feb;23(2):252-5. doi: 10.1038/ejhg.2014.103. Epub 2014 Jun 11. Eur J Hum Genet. 2015. PMID: 24916642 Free PMC article.
Impairment of adipose tissue in Prader-Willi syndrome rescued by growth hormone treatment.
Cadoudal T, Buléon M, Sengenès C, Diene G, Desneulin F, Molinas C, Eddiry S, Conte-Auriol F, Daviaud D, Martin PG, Bouloumié A, Salles JP, Tauber M, Valet P. Cadoudal T, et al. Among authors: conte auriol f. Int J Obes (Lond). 2014 Sep;38(9):1234-40. doi: 10.1038/ijo.2014.3. Epub 2014 Jan 10. Int J Obes (Lond). 2014. PMID: 24406482
19 results