Sequelae of GH Treatment in Children with PWS.
Tauber M, Diene G, Molinas C.
Pediatr Endocrinol Rev. 2016 Dec ;14(2):138-146. doi : 0.17458/PER.2016.TDM.SequelaeofGH.

• Autres articles récents :

Equivocal expression of emotions in children with Prader-Willi syndrome : what are the consequences for emotional abilities and social adjustment ?
Famelart N, Diene G, Çabal-Berthoumieu S, Glattard M, Molinas C, Guidetti M, Tauber M.
Orphanet J Rare Dis. 2020 Feb 21 ;15(1):55. doi : 10.1186/s13023-020-1333-9.

A study of voice and non-voice processing in Prader-Willi syndrome.
Strenilkov K, Debladis J, Salles J, Valette M, Mantoulan C, Thuilleaux D, Laurier V, Molinas C, Barone P, Tauber M.
Orphanet J Rare Dis. 2020 Jan 20 ;15(1):22. doi : 10.1186/s13023-020-1298-8.

Face processing and exploration of social signals in Prader-Willi syndrome : a genetic signature.
Debladis J, Valette M, Strenilkov K, Mantoulan C, Thuilleaux D, Laurier V, Molinas C, Barone P, Tauber M.
Orphanet J Rare Dis. 2019 Nov 15 ;14(1):262. doi : 10.1186/s13023-019-1221-3.

Effect of topiramate on eating behaviours in Prader-Willi syndrome : TOPRADER double-blind randomised placebo-controlled study.
Consoli A, Çabal Berthoumieu S, Raffin M, Thuilleaux D, Poitou C, Coupaye M, Pinto G, Lebbah S, Zahr N, Tauber M, Cohen D, Bonnot O.
Transl Psychiatry. 2019 Nov 4 ;9(1):274. doi : 10.1038/s41398-019-0597-0.

Causes of death in Prader-Willi syndrome : lessons from 11 years’ experience of a national reference center.
Pacoricona Alfaro DL, Lemoine P, Ehlinger V, Molinas C, Diene G, Valette M, Pinto G, Coupaye M, Poitou-Bernert C, Thuilleaux D, Arnaud C, Tauber M.
Orphanet J Rare Dis. 2019 Nov 4 ;14(1):238. doi : 10.1186/s13023-019-1214-2.

A model to characterize psychopathological features in adults with Prader-Willi syndrome.
Thuilleaux D, Laurier V, Copet P, Tricot J, Demeer G, Mourre F, Tauber M, Jauregi J.
Am J Med Genet A. 2018 Jan ;176(1):41-47. doi : 10.1002/ajmg.a.38525. Epub 2017 Nov 17.

Dyssynchrony and perinatal psychopathology impact of child disease on parents-child interactions, the paradigm of Prader Willi syndrom.
Viaux-Savelon S, Rosenblum O, Guedeney A, Diene G, Çabal-Berthoumieu S, Fichaux-Bourin P, Molinas C, Faye S, Valette M, Bascoul C, Cohen D, Tauber M.
J Physiol Paris. 2016 Nov ;110(4 Pt B):427-433. doi : 10.1016/j.jphysparis.2017.08.001.

Early diagnosis and care is achieved but should be improved in infants with Prader-Willi syndrome.
Bar C, Diene G, Molinas C, Bieth E, Casper C, Tauber M.
Orphanet J Rare Dis. 2017 Jun 28 ;12(1):118. doi : 10.1186/s13023-017-0673-6.

The Use of Oxytocin to Improve Feeding and Social Skills in Infants With Prader-Willi Syndrome.
Tauber M, Boulanouar K, Diene G, Çabal-Berthoumieu S, Ehlinger V, Fichaux-Bourin P, Molinas C, Faye S, Valette M, Pourrinet J, Cessans C, Viaux-Sauvelon S, Bascoul C, Guedeney A, Delhanty P, Geenen V, Martens H, Muscatelli F, Cohen D, Consoli A, Payoux P, Arnaud C, Salles JP.
Pediatrics. 2017 Feb ;139(2). pii : e20162976. doi : 10.1542/peds.2016-2976.

Autres articles publiés par le CR et/ou en partenariat avec le CR :

• Letter regarding "Prevalence of growth hormone deficiency in previously GH-treated young adults with Prader-Willi syndrome" by Donze et al.
  Höybye C, Tauber M, Angulo MA, Eiholzer U, Driscoll DJ, Cassidy SB, Holland AJ ; Clinical & Scientific Advisory Board of The International Prader-Willi Syndrome Organisation.
  Clin Endocrinol (Oxf). 2019 Oct ;91(4):578-579. doi : 10.1111/cen.14047.

• Impact of transitional care on endocrine and anthropometric parameters in Prader-Willi syndrome.
  Paepegaey AC, Coupaye M, Jaziri A, Ménesguen F, Dubern B, Polak M, Oppert JM, Tauber M, Pinto G, Poitou C.
  Endocr Connect. 2018 May ;7(5):663-672. doi : 10.1530/EC-18-0089.

• AZP-531, an unacylated ghrelin analog, improves food-related behavior in patients with Prader-Willi syndrome : A randomized placebo-controlled trial.
  Allas S, Caixàs A, Poitou C, Coupaye M, Thuilleaux D, Lorenzini F, Diene G, Crinò A, Illouz F, Grugni G, Potvin D, Bocchini S, Delale T, Abribat T, Tauber M.
  PLoS One. 2018 Jan 10 ;13(1):e0190849. doi : 10.1371/journal.pone.0190849.

• Deficiency in prohormone convertase PC1 impairs prohormone processing in Prader-Willi syndrome.
  Burnett LC, LeDuc CA, Sulsona CR, Paull D, Rausch R, Eddiry S, Carli JF, Morabito MV, Skowronski AA, Hubner G, Zimmer M, Wang L, Day R, Levy B, Fennoy I, Dubern B, Poitou C, Clement K, Butler MG, Rosenbaum M, Salles JP, Tauber M, Driscoll DJ, Egli D, Leibel RL.
  J Clin Invest. 2017 Jan 3 ;127(1):293-305. doi : 10.1172/JCI88648.

• Bridging the gap : metabolic and endocrine care of patients during transition.
  Hokken-Koelega A, van der Lely AJ, Hauffa B, Häusler G, Johannsson G, Maghnie M, Argente J, DeSchepper J, Gleeson H, Gregory JW, Höybye C, Keleştimur F, Luger A, Müller HL, Neggers S, Popovic-Brkic V, Porcu E, Sävendahl L, Shalet S, Spiliotis B, Tauber M.
  Endocr Connect. 2016 Nov ;5(6):R44-R54.

• Induced pluripotent stem cells (iPSC) created from skin fibroblasts of patients with Prader-Willi syndrome (PWS) retain the molecular signature of PWS.
  Burnett LC, LeDuc CA, Sulsona CR, Paull D, Eddiry S, Levy B, Salles JP, Tauber M, Driscoll DJ, Egli D, Leibel RL.
  Stem Cell Res. 2016 Nov ;17(3):526-530. doi : 10.1016/j.scr.2016.08.008.

• Effect of Genotype and Previous GH Treatment on Adiposity in Adults With Prader-Willi Syndrome.
  Coupaye M, Tauber M, Cuisset L, Laurier V, Bieth E, Lacorte JM, Oppert JM, Clément K, Poitou C.
  J Clin Endocrinol Metab. 2016 Dec ;101(12):4895-4903.

• Copy number variation analysis in adults with catatonia confirms haploinsufficiency of SHANK3 as a predisposing factor.
  Breckpot J, Vercruyssen M, Weyts E, Vandevoort S, D’Haenens G, Van Buggenhout G, Leempoels L, Brischoux-Boucher E, Van Maldergem L, Renieri A, Mencarelli MA, D’Angelo C, Mericq V, Hoffer MJ, Tauber M, Molinas C, Castiglioni C, Brison N, Vermeesch JR, Danckaerts M, Sienaert P, Devriendt K, Vogels A.
  Eur J Med Genet. 2016 Sep ;59(9):436-43. doi : 10.1016/j.ejmg.2016.08.003.

• Loss of Magel2 impairs the development of hypothalamic Anorexigenic circuits.
  Maillard J, Park S, Croizier S, Vanacker C, Cook JH, Prevot V, Tauber M, Bouret SG.
  Hum Mol Genet. 2016 Aug 1 ;25(15):3208-3215. doi : 10.1093/hmg/ddw169.

• Economic burden and health-related quality of life associated with Prader-Willi syndrome in France.
  Chevreul K, Berg Brigham K, Clément MC, Poitou C, Tauber M ; Members of the BURQOL-RD Research Network listed in the Online Appendix.
  J Intellect Disabil Res. 2016 Sep ;60(9):879-90. doi : 10.1111/jir.12288.

• High unacylated ghrelin levels support the concept of anorexia in infants with prader-willi syndrome.
  Beauloye V, Diene G, Kuppens R, Zech F, Winandy C, Molinas C, Faye S, Kieffer I, Beckers D, Nergårdh R, Hauffa B, Derycke C, Delhanty P, Hokken-Koelega A, Tauber M.
  Orphanet J Rare Dis. 2016 May 4 ;11(1):56. doi : 10.1186/s13023-016-0440-0.

• Deficits in voice and multisensory processing in patients with Prader-Willi syndrome.
  Salles J, Strelnikov K, Carine M, Denise T, Laurier V, Molinas C, Tauber M, Barone P.
  Neuropsychologia. 2016 May ;85:137-47. doi : 10.1016/j.neuropsychologia.2016.03.015.

• Hypothalamus and behavior : the model Prader-Willi syndrome.
  Tauber M.
  Rev Prat. 2015 Dec ;65(10):1273-4.

• Laparoscopic sleeve gastrectomy in children and adolescents with Prader-Willi Syndrome : a matched control study.
  Coupaye M, Poitou C, Tauber M.
  Surg Obes Relat Dis. 2016 Jan ;12(1):213-4. doi : 10.1016/j.soard.2015.09.015.

• Psychotropic treatments in Prader-Willi syndrome : a critical review of published literature.
  Bonnot O, Cohen D, Thuilleaux D, Consoli A, Cabal S, Tauber M.
  Eur J Pediatr. 2016 Jan ;175(1):9-18. doi : 10.1007/s00431-015-2670-x.

• Prader-Willi syndrome in 2015.
  Tauber M, Thuilleaux D, Bieth É.
  Med Sci (Paris). 2015 Oct ;31(10):853-60. doi : 10.1051/medsci/20153110011.

• Elevated ratio of acylated to unacylated ghrelin in children and young adults with Prader-Willi syndrome.
  Kuppens RJ, Diène G, Bakker NE, Molinas C, Faye S, Nicolino M, Bernoux D, Delhanty PJ, van der Lely AJ, Allas S, Julien M, Delale T, Tauber M, Hokken-Koelega AC.
  Endocrine. 2015 Dec ;50(3):633-42. doi : 10.1007/s12020-015-0614-x.

• Haploinsufficiency of the miR-873/miR-876 microRNA cluster is associated with craniofacial abnormalities.
  Koufaris C, Papagregoriou G, Kousoulidou L, Moutafi M, Tauber M, Jouret B, Kieffer I, Deltas C, Tanteles GA, Anastasiadou V, Patsalis PC, Sismani C.
  Gene. 2015 Apr 25 ;561(1):95-100. doi : 10.1016/j.gene.2015.02.018.

• An Early Postnatal Oxytocin Treatment Prevents Social and Learning Deficits in Adult Mice Deficient for Magel2, a Gene Involved in Prader-Willi Syndrome and Autism.
  Meziane H, Schaller F, Bauer S, Villard C, Matarazzo V, Riet F, Guillon G, Lafitte D, Desarmenien MG, Tauber M, Muscatelli F.
  Biol Psychiatry. 2015 Jul 15 ;78(2):85-94. doi : 10.1016/j.biopsych.2014.11.010.

• Medical, psychological and social features in a large cohort of adults with Prader-Willi syndrome : experience from a dedicated centre in France.
  Laurier V, Lapeyrade A, Copet P, Demeer G, Silvie M, Bieth E, Coupaye M, Poitou C, Lorenzini F, Labrousse F, Molinas C, Tauber M, Thuilleaux D, Jauregi J.
  J Intellect Disabil Res. 2015 May ;59(5):411-21. doi : 10.1111/jir.12140.

• 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.
  Eur J Hum Genet. 2015 Feb ;23(2):252-5. doi : 10.1038/ejhg.2014.103.

• Ontogenesis of oxytocin pathways in the mammalian brain : late maturation and psychosocial disorders.
  Grinevich V, Desarménien MG, Chini B, Tauber M, Muscatelli F.
  Front Neuroanat. 2015 Jan 20 ;8:164. doi : 10.3389/fnana.2014.00164. eCollection 2014.