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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: tauber m. 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
French database of children and adolescents with Prader-Willi syndrome.
Molinas C, Cazals L, Diene G, Glattard M, Arnaud C, Tauber M; French Reference Centre for PWS (FrRefC-PWS). Molinas C, et al. Among authors: tauber m. BMC Med Genet. 2008 Oct 2;9:89. doi: 10.1186/1471-2350-9-89. BMC Med Genet. 2008. PMID: 18831731 Free PMC article.
Oxytocin may be useful to increase trust in others and decrease disruptive behaviours in patients with Prader-Willi syndrome: a randomised placebo-controlled trial in 24 patients.
Tauber M, Mantoulan C, Copet P, Jauregui J, Demeer G, Diene G, Rogé B, Laurier V, Ehlinger V, Arnaud C, Molinas C, Thuilleaux D. Tauber M, et al. Orphanet J Rare Dis. 2011 Jun 24;6:47. doi: 10.1186/1750-1172-6-47. Orphanet J Rare Dis. 2011. PMID: 21702900 Free PMC article. Clinical Trial.
Hyperphagia: current concepts and future directions proceedings of the 2nd international conference on hyperphagia.
Heymsfield SB, Avena NM, Baier L, Brantley P, Bray GA, Burnett LC, Butler MG, Driscoll DJ, Egli D, Elmquist J, Forster JL, Goldstone AP, Gourash LM, Greenway FL, Han JC, Kane JG, Leibel RL, Loos RJ, Scheimann AO, Roth CL, Seeley RJ, Sheffield V, Tauber M, Vaisse C, Wang L, Waterland RA, Wevrick R, Yanovski JA, Zinn AR. Heymsfield SB, et al. Among authors: tauber m. Obesity (Silver Spring). 2014 Feb;22 Suppl 1(0 1):S1-S17. doi: 10.1002/oby.20646. Obesity (Silver Spring). 2014. PMID: 24574081 Free PMC article.
Prader-Willi syndrome as a model of human hyperphagia.
Tauber M, Diene G, Mimoun E, Çabal-Berthoumieu S, Mantoulan C, Molinas C, Muscatelli F, Salles JP. Tauber M, et al. Front Horm Res. 2014;42:93-106. doi: 10.1159/000358317. Epub 2014 Apr 7. Front Horm Res. 2014. PMID: 24732928 Review.
Clinical utility gene card for: Prader-Willi Syndrome.
Buiting K, Cassidy SB, Driscoll DJ, Gillessen-Kaesbach G, Kanber D, Tauber M, Schwinger E, Horsthemke B. Buiting K, et al. Among authors: tauber m. Eur J Hum Genet. 2014 Sep;22(9). doi: 10.1038/ejhg.2014.66. Epub 2014 Apr 16. Eur J Hum Genet. 2014. PMID: 24736734 Free PMC article. No abstract available.
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: tauber m. 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.
754 results