Demily C - Search Results

1

Noninvasive electrical stimulation for psychiatric care in Down syndrome.

Brunelin J, Adam O, Favre E, Prange S, Zante E, Demily C. Brunelin J, et al. Among authors: demily c. Brain Stimul. 2022 May-Jun;15(3):678-679. doi: 10.1016/j.brs.2022.04.012. Epub 2022 Apr 22. Brain Stimul. 2022. PMID: 35470018 Free article. No abstract available.

2

Social cognition in Wilson's disease: A new phenotype?

Peyroux E, Santaella N, Broussolle E, Rigard C, Favre E, Brunet AS, Bost M, Lachaux A, Demily C. Peyroux E, et al. Among authors: demily c. PLoS One. 2017 Apr 6;12(4):e0173467. doi: 10.1371/journal.pone.0173467. eCollection 2017. PLoS One. 2017. PMID: 28384152 Free PMC article.

3

An ambiguous psychiatric diagnosis resolved by genetic investigations.

Poisson A, Favre E, Peyroux E, Nicolas A, Schlutz Bolard C, Demily C. Poisson A, et al. Among authors: demily c. Schizophr Res. 2018 May;195:577-578. doi: 10.1016/j.schres.2017.09.022. Epub 2017 Sep 21. Schizophr Res. 2018. PMID: 28943095 No abstract available.

4

Overview of Social Cognitive Dysfunctions in Rare Developmental Syndromes With Psychiatric Phenotype.

Morel A, Peyroux E, Leleu A, Favre E, Franck N, Demily C. Morel A, et al. Among authors: demily c. Front Pediatr. 2018 May 3;6:102. doi: 10.3389/fped.2018.00102. eCollection 2018. Front Pediatr. 2018. PMID: 29774207 Free PMC article. Review.

5

Computer-based cognitive remediation program for the treatment of behavioral problems in children with intellectual disability: the «COGNITUS & MOI» study protocol for a randomized controlled trial.

Favre E, Peyroux E, Babinet MN, Poisson A, Demily C. Favre E, et al. Among authors: demily c. BMC Psychiatry. 2018 Jul 20;18(1):235. doi: 10.1186/s12888-018-1810-z. BMC Psychiatry. 2018. PMID: 30029627 Free PMC article.

6

12q13.12q13.13 microdeletion encompassing ACVRL1 and SCN8A genes: Clinical report of a new contiguous gene syndrome.

Poisson A, Lesca G, Chatron N, Favre E, Cottin V, Gamondes D, Sanlaville D, Edery P, Giraud S, Demily C, Dupuis-Girod S. Poisson A, et al. Among authors: demily c. Eur J Med Genet. 2019 Nov;62(11):103565. doi: 10.1016/j.ejmg.2018.10.017. Epub 2018 Oct 30. Eur J Med Genet. 2019. PMID: 30389587

7

An implicit and reliable neural measure quantifying impaired visual coding of facial expression: evidence from the 22q11.2 deletion syndrome.

Leleu A, Favre E, Yailian A, Fumat H, Klamm J, Amado I, Baudouin JY, Franck N, Demily C. Leleu A, et al. Among authors: demily c. Transl Psychiatry. 2019 Feb 4;9(1):67. doi: 10.1038/s41398-019-0411-z. Transl Psychiatry. 2019. PMID: 30718458 Free PMC article.

8

What do error patterns in processing facial expressions, social interaction scenes and vocal prosody tell us about the way social cognition works in children with 22q11.2DS?

Peyroux E, Babinet MN, Cannarsa C, Madelaine C, Favre E, Demily C, Michael GA. Peyroux E, et al. Among authors: demily c. Eur Child Adolesc Psychiatry. 2020 Mar;29(3):299-313. doi: 10.1007/s00787-019-01345-1. Epub 2019 May 23. Eur Child Adolesc Psychiatry. 2020. PMID: 31123832

9

Exploratory case study of monozygotic twins with 22q11.2DS provides further clues to circumscribe neurocognitive markers of psychotic symptoms.

Favre E, Leleu A, Peyroux E, Baudouin JY, Franck N, Demily C. Favre E, et al. Among authors: demily c. Neuroimage Clin. 2019;24:101987. doi: 10.1016/j.nicl.2019.101987. Epub 2019 Aug 17. Neuroimage Clin. 2019. PMID: 31446315 Free PMC article.

10

[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.

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