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 :

Diabetes Mellitus in Prader-Willi Syndrome : Natural History during the Transition from Childhood to Adulthood in a Cohort of 39 Patients.
Clerc A, Coupaye M, Mosbah H, Pinto G, Laurier V, Mourre F, Merrien C, Diene G, Poitou C, Tauber M. J Clin Med. 2021 Nov 15 ;10(22):5310. doi : 10.3390/jcm10225310.

Developmental psychopharmacology : example of Prader-Willi syndrome.
Consoli A, Tauber M, Cohen D. Rev Prat. 2020 May ;70(5):507-508.

The RDoC approach for translational psychiatry : Could a genetic disorder with psychiatric symptoms help fill the matrix ? the example of Prader-Willi syndrome.
Salles J, Lacassagne E, Benvegnu G, Berthoumieu SÇ, Franchitto N, Tauber M. Transl Psychiatry. 2020 Aug 8 ;10(1):274. doi : 10.1038/s41398-020-00964-6.

What can we learn from PWS and SNORD116 genes about the pathophysiology of addictive disorders ?
Salles J, Lacassagne E, Eddiry S, Franchitto N, Salles JP, Tauber M. Mol Psychiatry. 2021 Jan ;26(1):51-59. doi : 10.1038/s41380-020-00917-x.

Endocrine disorders in Prader-Willi syndrome : a model to understand and treat hypothalamic dysfunction.
Tauber M, Hoybye C. Lancet Diabetes Endocrinol. 2021 Apr ;9(4):235-246. doi : 10.1016/S2213-8587(21)00002-4.

SNORD116 and growth hormone therapy impact IGFBP7 in Prader-Willi syndrome.
Eddiry S, Diene G, Molinas C, Salles J, Auriol FC, Gennero I, Bieth E, Skryabin BV, Rozhdestvensky TS, Burnett LC, Leibel RL, Tauber M, Salles JP. Genet Med. 2021 May 26. doi : 10.1038/s41436-021-01185-y.

Effects of the COVID-19 pandemic and lockdown on the mental and physical health of adults with Prader-Willi syndrome.
Mosbah H, Coupaye M, Jacques F, Tauber M, Clément K, Oppert JM, Poitou C. Orphanet J Rare Dis. 2021 May 5 ;16(1):202. doi : 10.1186/s13023-021-01833-1.

MECHANISMS IN ENDOCRINOLOGY : Update on treatments for patients with genetic obesity.
Poitou C, Mosbah H, Clément K. Eur J Endocrinol. 2020 Nov ;183(5):R149-R166.

Increasing physical activity in adult women with Prader-Willi syndrome : A transferability study.
Bellicha A, Coupaye M, Hocquaux L, Speter F, Oppert JM, Poitou C. J Appl Res Intellect Disabil. 2020 Mar ;33(2):258-267. doi : 10.1111/jar.12669.

Rare genetic forms of obesity : From gene to therapy.
Clément K, Mosbah H, Poitou C. Physiol Behav. 2020 Dec 1 ;227:113134.

Cognitive Training Targeting Planning Dysfunction in Adults with Prader-Willi Syndrome : Brief Report of a Study Protocol.
Estival S, Krasny-Pacini A, Laurier V, Maugard C, Thuilleaux D, Postal V. Dev Neurorehabil. 2019 Nov ;22(8):569-575. doi : 10.1080/17518423.2019.1642414.

Investigation of the relationship between electrodermal and behavioural responses to executive tasks in Prader-Willi syndrome : An event-related experiment.
Chevalère J, Jauregi J, Copet P, Laurier V, Thuilleaux D, Postal V. Res Dev Disabil. 2019 Feb ;85:229-242. doi : 10.1016/j.ridd.2018.11.013.

The influence of emotional contexts on mental flexibility in Prader-Willi syndrome.
Chevalère J, Camblats AM, Laurier V, Mourre F, Estival S, Postal V. J Intellect Disabil Res. 2021 Jan 25.

Prader-Willi syndrome : Hormone therapies.
Tauber M, Diene G. Handb Clin Neurol. 2021 ;181:351-367.

Physical Activity in Patients with Prader-Willi Syndrome-A Systematic Review of Observational and Interventional Studies.
Bellicha A, Coupaye M, Mosbah H, Tauber M, Oppert JM, Poitou C. J Clin Med. 2021 Jun 7 ;10(11):2528. doi : 10.3390/jcm10112528.

Effects of the COVID-19 pandemic and lockdown on the mental and physical health of adults with Prader-Willi syndrome.
Mosbah H, Coupaye M, Jacques F, Tauber M, Clément K, Oppert JM, Poitou C. Orphanet J Rare Dis. 2021 May 5 ;16(1):202. doi : 10.1186/s13023-021-01833-1.

Paradoxical low severity of COVID-19 in Prader-Willi syndrome : data from a French survey on 647 patients.
Coupaye M, Laurier V, Benvegnu G, Poitou C, Faucher P, Mosbah H, Diene G, Pinto G, Briceño LG, Merrien C, Toyos AC, Montastier E, Tauber M, Mourre F. Orphanet J Rare Dis. 2021 Jul 21 ;16(1):325. doi : 10.1186/s13023-021-01949-4.

Study of the deficit in planning abilities of adults with Prader-Willi Syndrome.
Estival S, Chevalère J, Laurier V, Mourre F, Tricot J, Postal V. Res Dev Disabil. 2021 Oct ;117:104056. doi : 10.1016/j.ridd.2021.104056.

Improvement of Planning Abilities in Adults with Prader-Willi Syndrome : A Randomized Controlled Trial.
Estival S, Laurier V, Mourre F, Postal V. Dev Neurorehabil. 2021 Oct ;24(7):478-493. doi : 10.1080/17518423.2021.1915405.

Patients with PWS and related syndromes display differentially methylated regions involved in neurodevelopmental and nutritional trajectory.
Salles J, Eddiry S, Lacassagne E, Laurier V, Molinas C, Bieth É, Franchitto N, Salles JP, Tauber M. Clin Epigenetics. 2021 Aug 13 ;13(1):159. doi : 10.1186/s13148-021-01143-0.

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 :

• Associations between cognitive performance and the rehabilitation, medical care and social support provided to French children with Prader-Willi syndrome.
  Roux-Levy PH, Bournez M, Masurel A, Jean N, Chancenotte S, Bordes M, Debomy F, Minot D, Schmitt E, Vinault S, Gautier E, Lacombe D, Odent S, Mikaty M, Manouvrier S, Ghoumid J, Geneviève D, Lehman N, Philip N, Edery P, Cornaton J, Gallard J, Héron D, Rastel C, Huet F, Thauvin-Robinet C, Verloes A, Binquet C, Tauber M, Lejeune C, Faivre L. Eur J Med Genet. 2020 Dec ;63(12):104064. doi : 10.1016/j.ejmg.2020.104064.

• Outcomes in children treated with growth hormone for Prader-Willi syndrome : data from the ANSWER Program and NordiNet International Outcome Study.
  Angulo M, Abuzzahab MJ, Pietropoli A, Ostrow V, Kelepouris N, Tauber M. Int J Pediatr Endocrinol. 2020 Nov 10 ;2020(1):20. doi : 10.1186/s13633-020-00090-6.

• Growth Restriction and Genomic Imprinting-Overlapping Phenotypes Support the Concept of an Imprinting Network.
  Eggermann T, Davies JH, Tauber M, van den Akker E, Hokken-Koelega A, Johansson G, Netchine I. Genes (Basel). 2021 Apr 17 ;12(4):585. doi : 10.3390/genes12040585.

• Gut microbiota of obese subjects with Prader-Willi syndrome is linked to metabolic health.
  Olsson LM, Poitou C, Tremaroli V, Coupaye M, Aron-Wisnewsky J, Bäckhed F, Clément K, Caesar R. Gut. 2020 Jul ;69(7):1229-1238. doi : 10.1136/gutjnl-2019-319322.

• Central Adrenal Insufficiency Is Rare in Adults With Prader-Willi Syndrome.
  Rosenberg AGW, Pellikaan K, Poitou C, Goldstone AP, Høybye C, Markovic T, Grugni G, Crinò A, Caixàs A, Coupaye M, Van Den Berg SAA, Van Der Lely AJ, De Graaff LCG. J Clin Endocrinol Metab. 2020 Jul 1 ;105(7):e2563-71. doi : 10.1210/clinem/dgaa168.

• Transition of young adults with endocrine and metabolic diseases : the ’TRANSEND’ cohort.
  Le Roux E, Menesguen F, Tejedor I, Popelier M, Halbron M, Faucher P, Malivoir S, Pinto G, Léger J, Hatem S, Polak M, Poitou C, Touraine P. Endocr Connect. 2021 Jan ;10(1):21-28.

• Implication of heterozygous variants in genes of the leptin-melanocortin pathway in severe obesity.
  Courbage S, Poitou C, Le Beyec-Le Bihan J, Karsenty A, Lemale J, Pelloux V, Lacorte JM, Carel JC, Lecomte N, Storey C, De Filippo G, Coupaye M, Oppert JM, Tounian P, Clément K, Dubern B. J Clin Endocrinol Metab. 2021 Jun 7:dgab404. doi : 10.1210/clinem/dgab404.

• Hyponatremia in Children and Adults with Prader-Willi Syndrome : A Survey Involving Seven Countries.
  Coupaye M, Pellikaan K, Goldstone AP, Crinò A, Grugni G, Markovic TP, Høybye C, Caixàs A, Mosbah H, De Graaff LCG, Tauber M, Poitou C. J Clin Med. 2021 Aug 12 ;10(16):3555. doi : 10.3390/jcm10163555.

• Growth Restriction and Genomic Imprinting-Overlapping Phenotypes Support the Concept of an Imprinting Network.
  Eggermann T, Davies JH, Tauber M, van den Akker E, Hokken-Koelega A, Johansson G, Netchine I. Genes (Basel). 2021 Apr 17 ;12(4):585. doi : 10.3390/genes12040585.

• Clinical management of patients with genetic obesity during COVID-19 pandemic : position paper of the ESE Growth & Genetic Obesity COVID-19 Study Group and Rare Endo-ERN main thematic group on Growth and Obesity.
  De Groot CJ, Poitou Bernert C, Coupaye M, Clement K, Paschou SA, Charmandari E, Kanaka-Gantenbein C, Wabitsch M, Buddingh EP, Nieuwenhuijsen B, Marina L, Johannsson G, Van Den Akker ELT. Endocrine. 2021 Mar ;71(3):653-662. doi : 10.1007/s12020-021-02619-y.

• Hypogonadism in Adult Males with Prader-Willi Syndrome-Clinical Recommendations Based on a Dutch Cohort Study, Review of the Literature and an International Expert Panel Discussion.
  Pellikaan K, Ben Brahim Y, Rosenberg AGW, Davidse K, Poitou C, Coupaye M, Goldstone AP, Høybye C, Markovic TP, Grugni G, Crinò A, Caixàs A, Eldar-Geva T, Hirsch HJ, Gross-Tsur V, Butler MG, Miller JL, van den Berg SAA, van der Lely AJ, de Graaff LCG. J Clin Med. 2021 Sep 24 ;10(19):4361. doi : 10.3390/jcm10194361.

• 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.