Molinas C - Search Results

1

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. Tauber M, et al. Among authors: molinas c. Pediatrics. 2017 Feb;139(2):e20162976. doi: 10.1542/peds.2016-2976. Pediatrics. 2017. PMID: 28100688 Clinical Trial.

2

Heterozygous mutation in the WSXWS equivalaent motif of the growth hormone receptor in a child with poor response to growth hormone therapy.

Tauber MT, Porra V, Dastot F, Molinas C, Amselem S, Cholin S, Rochiccioli P, Bieth E. Tauber MT, et al. Among authors: molinas c. Growth Horm IGF Res. 1998 Jun;8(3):211-6. doi: 10.1016/s1096-6374(98)80113-5. Growth Horm IGF Res. 1998. PMID: 10984309

3

Hyperghrelinemia is a common feature of Prader-Willi syndrome and pituitary stalk interruption: a pathophysiological hypothesis.

Tauber M, Conte Auriol F, Moulin P, Molinas C, Delagnes V, Salles JP. Tauber M, et al. Among authors: molinas c. Horm Res. 2004;62(1):49-54. doi: 10.1159/000078862. Epub 2004 Jun 8. Horm Res. 2004. PMID: 15192277

4

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. Bacheré N, et al. Among authors: molinas c. Horm Res. 2008;69(1):45-52. doi: 10.1159/000111795. Epub 2007 Dec 4. Horm Res. 2008. PMID: 18059083

5

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

Tauber M, Diene G, Molinas C, Hébert M. Tauber M, et al. Among authors: molinas c. Am J Med Genet A. 2008 Apr 1;146A(7):881-7. doi: 10.1002/ajmg.a.32131. Am J Med Genet A. 2008. PMID: 18324685 Review.

6

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: molinas c. 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

7

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. Odent T, et al. Among authors: molinas c. Pediatrics. 2008 Aug;122(2):e499-503. doi: 10.1542/peds.2007-3487. Epub 2008 Jul 7. Pediatrics. 2008. PMID: 18606625

8

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. BMC Med Genet. 2008 Oct 2;9:89. doi: 10.1186/1471-2350-9-89. BMC Med Genet. 2008. PMID: 18831731 Free PMC article.

9

Cognitive profile in a large French cohort of adults with Prader-Willi syndrome: differences between genotypes.

Copet P, Jauregi J, Laurier V, Ehlinger V, Arnaud C, Cobo AM, Molinas C, Tauber M, Thuilleaux D. Copet P, et al. Among authors: molinas c. J Intellect Disabil Res. 2010 Mar;54(3):204-15. doi: 10.1111/j.1365-2788.2010.01251.x. Epub 2010 Feb 2. J Intellect Disabil Res. 2010. PMID: 20136683

10

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. Diene G, et al. Among authors: molinas c. Horm Res Paediatr. 2010;74(2):121-8. doi: 10.1159/000313377. Epub 2010 Apr 15. Horm Res Paediatr. 2010. PMID: 20395666

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