Guinchat V - Search Results

1

CNOT2 haploinsufficiency in a 40-year-old man with intellectual disability, autism, and seizures.

Royer-Bertrand B, Cisarova K, Niel Bütschi F, Foletti G, Guinchat V, Tran C, Superti-Furga A, Good JM. Royer-Bertrand B, et al. Among authors: guinchat v. Am J Med Genet A. 2021 Aug;185(8):2602-2606. doi: 10.1002/ajmg.a.62343. Epub 2021 May 21. Am J Med Genet A. 2021. PMID: 34018673 Review. No abstract available.

2

[Complex situations in adults with severe intellectual disabilities - A new support model].

Guinchat V, Brébant AF, Chabane N. Guinchat V, et al. Rev Med Suisse. 2021 Sep 22;17(751):1611-1613. Rev Med Suisse. 2021. PMID: 34550654 French.

3

Paracentric inversion of chromosome 2 associated with cryptic duplication of 2q14 and deletion of 2q37 in a patient with autism.

Devillard F, Guinchat V, Moreno-De-Luca D, Tabet AC, Gruchy N, Guillem P, Nguyen Morel MA, Leporrier N, Leboyer M, Jouk PS, Lespinasse J, Betancur C. Devillard F, et al. Among authors: guinchat v. Am J Med Genet A. 2010 Sep;152A(9):2346-54. doi: 10.1002/ajmg.a.33601. Am J Med Genet A. 2010. PMID: 20684015 Free PMC article.

4

Multidisciplinary treatment plan for challenging behaviors in neurodevelopmental disorders.

Guinchat V, Cravero C, Lefèvre-Utile J, Cohen D. Guinchat V, et al. Handb Clin Neurol. 2020;174:301-321. doi: 10.1016/B978-0-444-64148-9.00022-3. Handb Clin Neurol. 2020. PMID: 32977887

5

Case Report: Opioid Use Disorder Associated With Low/Moderate Dose of Loperamide in an Intellectual Disability Patient With CYP3A and P-Glycoprotein Reduced Activity.

Guinchat V, Ansermot N, Ing Lorenzini K, Politis D, Daali Y, Eap CB, Crettol S. Guinchat V, et al. Front Psychiatry. 2022 Jun 23;13:910684. doi: 10.3389/fpsyt.2022.910684. eCollection 2022. Front Psychiatry. 2022. PMID: 35815036 Free PMC article.

6

Compressive Garments in Individuals with Autism and Severe Proprioceptive Dysfunction: A Retrospective Exploratory Case Series.

Guinchat V, Vlamynck E, Diaz L, Chambon C, Pouzenc J, Cravero C, Baeza-Velasco C, Hamonet C, Xavier J, Cohen D. Guinchat V, et al. Children (Basel). 2020 Jul 13;7(7):77. doi: 10.3390/children7070077. Children (Basel). 2020. PMID: 32668622 Free PMC article.

7

Trends, perinatal characteristics, and medical conditions in pervasive developmental disorders.

Guillem P, Cans C, Guinchat V, Ratel M, Jouk PS. Guillem P, et al. Among authors: guinchat v. Dev Med Child Neurol. 2006 Nov;48(11):896-900. doi: 10.1017/S0012162206001964. Dev Med Child Neurol. 2006. PMID: 17044957 Free article.

8

Risk factors of acute behavioral regression in psychiatrically hospitalized adolescents with autism.

Périsse D, Amiet C, Consoli A, Thorel MV, Gourfinkel-An I, Bodeau N, Guinchat V, Barthélémy C, Cohen D. Périsse D, et al. Among authors: guinchat v. J Can Acad Child Adolesc Psychiatry. 2010 May;19(2):100-8. J Can Acad Child Adolesc Psychiatry. 2010. PMID: 20467546 Free PMC article.

9

Pre-, peri- and neonatal risk factors for autism.

Guinchat V, Thorsen P, Laurent C, Cans C, Bodeau N, Cohen D. Guinchat V, et al. Acta Obstet Gynecol Scand. 2012 Mar;91(3):287-300. doi: 10.1111/j.1600-0412.2011.01325.x. Acta Obstet Gynecol Scand. 2012. PMID: 22085436 Free article. Review.

10

Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders.

Leblond CS, Heinrich J, Delorme R, Proepper C, Betancur C, Huguet G, Konyukh M, Chaste P, Ey E, Rastam M, Anckarsäter H, Nygren G, Gillberg IC, Melke J, Toro R, Regnault B, Fauchereau F, Mercati O, Lemière N, Skuse D, Poot M, Holt R, Monaco AP, Järvelä I, Kantojärvi K, Vanhala R, Curran S, Collier DA, Bolton P, Chiocchetti A, Klauck SM, Poustka F, Freitag CM, Waltes R, Kopp M, Duketis E, Bacchelli E, Minopoli F, Ruta L, Battaglia A, Mazzone L, Maestrini E, Sequeira AF, Oliveira B, Vicente A, Oliveira G, Pinto D, Scherer SW, Zelenika D, Delepine M, Lathrop M, Bonneau D, Guinchat V, Devillard F, Assouline B, Mouren MC, Leboyer M, Gillberg C, Boeckers TM, Bourgeron T. Leblond CS, et al. Among authors: guinchat v. PLoS Genet. 2012 Feb;8(2):e1002521. doi: 10.1371/journal.pgen.1002521. Epub 2012 Feb 9. PLoS Genet. 2012. PMID: 22346768 Free PMC article.

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