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Page 1
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. 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
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
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.
[New molecular mechanisms of growth hormone insensitivity].
Edouard T, Raynal P, Yart A, Conte-Auriol F, Salles JP, Tauber M. Edouard T, et al. 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.
[Osteogenesis factors in childhood].
Salles JP, Gennero I, Moulin P, Conte-Auriol F, Edouard T, Tauber M. Salles JP, et al. 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.
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
19 results