Demily C - Search Results

1

Complex phenotype with social communication disorder caused by mosaic supernumerary ring chromosome 19p.

Demily C, Rossi M, Chesnoy-Servanin G, Martin B, Poisson A, Sanlaville D, Edery P. Demily C, et al. BMC Med Genet. 2014 Dec 11;15:132. doi: 10.1186/s12881-014-0132-3. BMC Med Genet. 2014. PMID: 25496186 Free PMC article.

2

[Neurocognitive and psychiatric management of the 22q11.2 deletion syndrome].

Demily C, Rossi M, Schneider M, Edery P, Leleu A, d'Amato T, Franck N, Eliez S. Demily C, et al. Encephale. 2015 Jun;41(3):266-73. doi: 10.1016/j.encep.2014.10.005. Epub 2014 Dec 16. Encephale. 2015. PMID: 25523123 Review. French.

3

[Smith-Magenis syndrome is an association of behavioral and sleep/wake circadian rhythm disorders].

Poisson A, Nicolas A, Sanlaville D, Cochat P, De Leersnyder H, Rigard C, Franco P, des Portes V, Edery P, Demily C. Poisson A, et al. Among authors: demily c. Arch Pediatr. 2015 Jun;22(6):638-45. doi: 10.1016/j.arcped.2015.03.015. Epub 2015 Apr 28. Arch Pediatr. 2015. PMID: 25934608 French.

4

Facial emotion perception by intensity in children and adolescents with 22q11.2 deletion syndrome.

Leleu A, Saucourt G, Rigard C, Chesnoy G, Baudouin JY, Rossi M, Edery P, Franck N, Demily C. Leleu A, et al. Among authors: demily c. Eur Child Adolesc Psychiatry. 2016 Mar;25(3):297-310. doi: 10.1007/s00787-015-0741-1. Epub 2015 Jul 7. Eur Child Adolesc Psychiatry. 2016. PMID: 26149605

5

Behavioral disturbance and treatment strategies in Smith-Magenis syndrome.

Poisson A, Nicolas A, Cochat P, Sanlaville D, Rigard C, de Leersnyder H, Franco P, Des Portes V, Edery P, Demily C. Poisson A, et al. Among authors: demily c. Orphanet J Rare Dis. 2015 Sep 4;10:111. doi: 10.1186/s13023-015-0330-x. Orphanet J Rare Dis. 2015. PMID: 26336863 Free PMC article.

6

«Cognitus & Moi»: A Computer-Based Cognitive Remediation Program for Children with Intellectual Disability.

Demily C, Rigard C, Peyroux E, Chesnoy-Servanin G, Morel A, Franck N. Demily C, et al. Front Psychiatry. 2016 Feb 3;7:10. doi: 10.3389/fpsyt.2016.00010. eCollection 2016. Front Psychiatry. 2016. PMID: 26869942 Free PMC article.

7

16q12.2q21: A new susceptibility locus for schizophrenia?

Poisson A, Schluth Bolard C, Martin B, Babinet MN, Sanlaville D, Demily C. Poisson A, et al. Among authors: demily c. Schizophr Res. 2016 Dec;178(1-3):109-111. doi: 10.1016/j.schres.2016.09.007. Epub 2016 Sep 8. Schizophr Res. 2016. PMID: 27617415 No abstract available.

8

Low dose clozapine controls adult-onset psychosis associated with the neurogenic ataxia-retinitis pigmentosa (NARP) mutation.

Demily C, Duwime C, Poisson A, Boddaert N, Munnich A. Demily C, et al. Mol Genet Metab Rep. 2016 Dec 13;10:20-22. doi: 10.1016/j.ymgmr.2016.12.003. eCollection 2017 Mar. Mol Genet Metab Rep. 2016. PMID: 28003964 Free PMC article. No abstract available.

9

Autism spectrum disorder associated with 49,XYYYY: case report and review of the literature.

Demily C, Poisson A, Peyroux E, Gatellier V, Nicolas A, Rigard C, Schluth-Bolard C, Sanlaville D, Rossi M. Demily C, et al. BMC Med Genet. 2017 Jan 31;18(1):9. doi: 10.1186/s12881-017-0371-1. BMC Med Genet. 2017. PMID: 28137251 Free PMC article. Review.

10

Authors' reply - Clozapine for mitochondrial psychosis.

Demily C, Duwime C, Poisson A, Boddaert N, Munnich A. Demily C, et al. Mol Genet Metab Rep. 2017 Feb 6;10:101. doi: 10.1016/j.ymgmr.2017.01.012. eCollection 2017 Mar. Mol Genet Metab Rep. 2017. PMID: 28224085 Free PMC article. No abstract available.

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