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Items: 40

1.

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.

2.

Evolution of Hip Dysplasia in Pediatric Patients With Prader-Willi Syndrome Treated With Growth Hormone Early in Development.

Laumonerie P, Tibbo ME, Ibnoulkhatib A, Kerezoudis P, Diene G, Thevenin Lemoine C, Accadbled F, Sales de Gauzy J.

J Pediatr Orthop. 2019 Aug 30. doi: 10.1097/BPO.0000000000001443. [Epub ahead of print]

PMID:
31479030
3.

Prader-Willi syndrome: A model for understanding the ghrelin system.

Tauber M, Coupaye M, Diene G, Molinas C, Valette M, Beauloye V.

J Neuroendocrinol. 2019 Jul;31(7):e12728. doi: 10.1111/jne.12728. Epub 2019 May 23. Review.

PMID:
31046160
4.

Growth Hormone Treatment for Prader-Willi Syndrome.

Tauber M, Diene G, Molinas C.

Pediatr Endocrinol Rev. 2018 Sep;16(Suppl 1):91-99. doi: 10.17458/per.vol16.2018.tdm.ghpraderwilli.

PMID:
30378786
5.

Noonan syndrome males display Sertoli cell-specific primary testicular insufficiency.

Moniez S, Pienkowski C, Lepage B, Hamdi S, Daudin M, Oliver I, Jouret B, Cartault A, Diene G, Verloes A, Cavé H, Salles JP, Tauber M, Yart A, Edouard T.

Eur J Endocrinol. 2018 Dec 1;179(6):409-418. doi: 10.1530/EJE-18-0582.

PMID:
30325180
6.

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. eCollection 2018.

7.

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. Epub 2017 Sep 1.

PMID:
28823614
8.

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.

9.

Sequelae of GH Treatment in Children with PWS.

Tauber M, Diene G, Molinas C.

Pediatr Endocrinol Rev. 2016 Dec;14(2):138-146. doi: 10.17458/PER.2016.TDM.SequelaeofGH. Review.

PMID:
28508607
10.

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.

11.

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.

12.

Pituitary Stalk Interruption Syndrome from Infancy to Adulthood: Clinical, Hormonal, and Radiological Assessment According to the Initial Presentation.

Bar C, Zadro C, Diene G, Oliver I, Pienkowski C, Jouret B, Cartault A, Ajaltouni Z, Salles JP, Sevely A, Tauber M, Edouard T.

PLoS One. 2015 Nov 12;10(11):e0142354. doi: 10.1371/journal.pone.0142354. eCollection 2015.

13.

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. Epub 2015 May 20.

14.

New candidate loci identified by array-CGH in a cohort of 100 children presenting with syndromic obesity.

Vuillaume ML, Naudion S, Banneau G, Diene G, Cartault A, Cailley D, Bouron J, Toutain J, Bourrouillou G, Vigouroux A, Bouneau L, Nacka F, Kieffer I, Arveiler B, Knoll-Gellida A, Babin PJ, Bieth E, Jouret B, Julia S, Sarda P, Geneviève D, Faivre L, Lacombe D, Barat P, Tauber M, Delrue MA, Rooryck C.

Am J Med Genet A. 2014 Aug;164A(8):1965-75. doi: 10.1002/ajmg.a.36587. Epub 2014 Apr 29.

PMID:
24782328
15.

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.

Front Horm Res. 2014;42:93-106. doi: 10.1159/000358317. Epub 2014 Apr 7. Review.

PMID:
24732928
16.

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.

Int J Obes (Lond). 2014 Sep;38(9):1234-40. doi: 10.1038/ijo.2014.3. Epub 2014 Jan 10.

PMID:
24406482
17.

Growth hormone therapy for children and adolescents with Prader-Willi syndrome is associated with improved body composition and metabolic status in adulthood.

Coupaye M, Lorenzini F, Lloret-Linares C, Molinas C, Pinto G, Diene G, Mimoun E, Demeer G, Labrousse F, Jauregi J, Laurier V, Basdevant A, Polak M, Thuilleaux D, Tauber M, Poitou C.

J Clin Endocrinol Metab. 2013 Feb;98(2):E328-35. doi: 10.1210/jc.2012-2881. Epub 2013 Jan 2.

PMID:
23284006
18.

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.

Orphanet J Rare Dis. 2011 Jun 24;6:47. doi: 10.1186/1750-1172-6-47.

19.

Efficacy of modafinil on excessive daytime sleepiness in Prader-Willi syndrome.

De Cock VC, Diene G, Molinas C, Masson VD, Kieffer I, Mimoun E, Tiberge M, Tauber M.

Am J Med Genet A. 2011 Jul;155A(7):1552-7. doi: 10.1002/ajmg.a.34047. Epub 2011 Jun 10.

PMID:
21671379
20.

Elevated insulin-like growth factor-I values in children with Prader-Willi syndrome compared with growth hormone (GH) deficiency children over two years of GH treatment.

Feigerlová E, Diene G, Oliver I, Gennero I, Salles JP, Arnaud C, Tauber M.

J Clin Endocrinol Metab. 2010 Oct;95(10):4600-8. doi: 10.1210/jc.2009-1831.

PMID:
20926543
21.

PET scan perfusion imaging in the Prader-Willi syndrome: new insights into the psychiatric and social disturbances.

Mantoulan C, Payoux P, Diene G, Glattard M, Rogé B, Molinas C, Sevely A, Zilbovicius M, Celsis P, Tauber M.

J Cereb Blood Flow Metab. 2011 Jan;31(1):275-82. doi: 10.1038/jcbfm.2010.87. Epub 2010 Jun 30.

22.

Endocrine disorders in children with Prader-Willi syndrome--data from 142 children of the French database.

Diene G, Mimoun E, Feigerlova E, Caula S, Molinas C, Grandjean H, Tauber M; French Reference Centre for PWS.

Horm Res Paediatr. 2010;74(2):121-8. doi: 10.1159/000313377. Epub 2010 Apr 15.

PMID:
20395666
23.

[Child obesity].

Tauber M, Jouret B, Diene G.

Rev Prat. 2009 Sep 20;59(7):1005-12. French. No abstract available.

PMID:
19839478
24.

[Early education for children with Prader-Willi syndrome].

Fichaux-Bourin P, Diène G, Glattard M, Tauber M.

Rev Laryngol Otol Rhinol (Bord). 2009;130(1):35-40. French.

PMID:
19530522
25.

[Severe delayed apnea in neonates and Prader-Willi syndrome: 2 case studies].

Vintéjoux A, Montagnon G, Diene G, Gouyon JB, Huet F.

Arch Pediatr. 2009 Mar;16(3):248-51. doi: 10.1016/j.arcped.2008.12.017. Epub 2009 Feb 4. French.

PMID:
19195855
26.

Is scoliosis an issue for giving growth hormone to children with Prader-Willi syndrome?

Diene G, de Gauzy JS, Tauber M.

Arch Dis Child. 2008 Dec;93(12):1004-6. doi: 10.1136/adc.2008.141390. No abstract available.

PMID:
19028967
27.

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).

BMC Med Genet. 2008 Oct 2;9:89. doi: 10.1186/1471-2350-9-89.

28.

Scoliosis in patients with Prader-Willi Syndrome.

Odent T, Accadbled F, Koureas G, Cournot M, Moine A, Diene G, Molinas C, Pinto G, Tauber M, Gomes B, de Gauzy JS, Glorion C.

Pediatrics. 2008 Aug;122(2):e499-503. doi: 10.1542/peds.2007-3487. Epub 2008 Jul 7.

PMID:
18606625
29.

Hyperghrelinemia precedes obesity in Prader-Willi syndrome.

Feigerlová E, Diene G, Conte-Auriol F, Molinas C, Gennero I, Salles JP, Arnaud C, Tauber M.

J Clin Endocrinol Metab. 2008 Jul;93(7):2800-5. doi: 10.1210/jc.2007-2138. Epub 2008 May 6.

PMID:
18460565
30.

Review of 64 cases of death in children with Prader-Willi syndrome (PWS).

Tauber M, Diene G, Molinas C, Hébert M.

Am J Med Genet A. 2008 Apr 1;146A(7):881-7. doi: 10.1002/ajmg.a.32131. Review.

PMID:
18324685
31.

Complications of scoliosis surgery in Prader-Willi syndrome.

Accadbled F, Odent T, Moine A, Chau E, Glorion C, Diene G, de Gauzy JS.

Spine (Phila Pa 1976). 2008 Feb 15;33(4):394-401. doi: 10.1097/BRS.0b013e318163fa24.

PMID:
18277871
32.

Necdin plays a role in the serotonergic modulation of the mouse respiratory network: implication for Prader-Willi syndrome.

Zanella S, Watrin F, Mebarek S, Marly F, Roussel M, Gire C, Diene G, Tauber M, Muscatelli F, Hilaire G.

J Neurosci. 2008 Feb 13;28(7):1745-55. doi: 10.1523/JNEUROSCI.4334-07.2008.

33.

Early diagnosis and multidisciplinary care reduce the hospitalization time and duration of tube feeding and prevent early obesity in PWS infants.

Bacheré N, Diene G, Delagnes V, Molinas C, Moulin P, Tauber M.

Horm Res. 2008;69(1):45-52. Epub 2007 Dec 4.

PMID:
18059083
34.

[The Prader-Willi syndrome].

Diene G, Postel-Vinay A, Pinto G, Polak M, Tauber M.

Ann Endocrinol (Paris). 2007 Jun;68(2-3):129-37. Epub 2007 May 17. Review. French.

PMID:
17499572
35.

A case of trisomy 12 mosaicism with pituitary malformation and polycystic ovary syndrome.

Boulard S, Diene G, Barat R, Oliver I, Pienkowski C, Lacombe D, Vincent MC, Bourrouillou G, Tauber M.

Genet Couns. 2006;17(2):173-83. Review.

PMID:
16970035
36.

Long-term evolution of endocrine disorders and effect of GH therapy in 35 patients with pituitary stalk interruption syndrome.

Tauber M, Chevrel J, Diene G, Moulin P, Jouret B, Oliver I, Pienkowski C, Sevely A.

Horm Res. 2005;64(6):266-73. Epub 2005 Oct 15.

PMID:
16260897
37.

[Use of polyunsaturated phosphatidylcholine (EPL) in combination with vitamin B complex in therapy of liver diseases].

Sorrentino F, Diene G, Corvaja E, Magnano V.

Clin Ter. 1982 Jul 31;102(2):163-83. Italian. No abstract available.

PMID:
7140175
38.

[Use of cloridarol in coronary insufficiency].

Mossuti E, Nigro P, Diene G, Petralito A.

Minerva Med. 1976 Apr 30;67(21):1394-7. Italian.

PMID:
934497
39.

[Recent contribution to the study on the effects of hexobendine in the treatment of coronary insufficiency].

Diene G, Nigro P, Cottini E, Andreozzi GM, Mossuti E, Sorrentino F.

Boll Soc Ital Cardiol. 1973;18(12):1213-21. Italian. No abstract available.

PMID:
4619973
40.

[Behavior of serum gamma glutamyl transpeptidase activity during acute phase of myocardial infarct].

Nicotra G, La Rosa G, Petralito A, Diene G, Sorrentino F.

Boll Soc Ital Cardiol. 1973;18(12):1222-30. Italian. No abstract available.

PMID:
4157138

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