Vincent Guinchat

Publications | Mémoires et thèses

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33 publications

 
Impact of somatosensory orthoses on behavioral and postural control in individuals with autism and severe proprioceptive dysfunction: an open exploratory trial
Guinchat V., Vlamynck E., Diaz L., Chambon C., Pouzenc J., Cravero C., Baeza-Velasco C., Hamonet C., Xavier J., Cohen D., en cours de soumission.
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 C.B., Crettol S., 2022. Frontiers in psychiatry, 13 p. 910684. Peer-reviewed.
Editorial: Neurodevelopmental, neuropsychiatric and psychosocial correlates of joint hypermobility and related disorders.
Guinchat V., Baeza-Velasco C., Bulbena A., Castori M., 2022. Frontiers in psychiatry, 13 p. 1109515. Peer-reviewed.
Situations complexes chez l’adulte avec déficience intellectuelle sévère - Un nouveau modèle d’accompagnement [Complex situations in adults with severe intellectual disabilities - A new support model]
Guinchat V., Brébant A.F., Chabane N., 2021/09/22. Revue medicale suisse, 17 (751) pp. 1611-1613. Peer-reviewed.
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 J.M., 2021/08. American journal of medical genetics. Part A, 185 (8) pp. 2602-2606. Peer-reviewed.
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., 2020/07/13. Children, 7 (7). Peer-reviewed.
 
Multidisciplinary treatment plan for challenging behaviors in neurodevelopmental disorders.
Guinchat V., Cravero C., Lefèvre-Utile J., Cohen D., 2020. Handbook of clinical neurology, 174 pp. 301-321. Peer-reviewed.
 
Developmental Phenotype of the Rare Case of DJ Caused by a Unique ADNP Gene De Novo Mutation.
Levine J., Cohen D., Herman C., Verloes A., Guinchat V., Diaz L., Cravero C., Mandel A., Gozes I., 2019/07. Journal of molecular neuroscience, 68 (3) pp. 321-330. Peer-reviewed.
 
Changes in the Use of Emergency Care for the Youth With Mental Health Problems Over Decades: A Repeated Cross Sectional Study
Benarous Xavier, Milhiet Vanessa, Oppetit Alice, Viaux Sylvie, El Kamel Nadjia Mahi, Guinchat Vincent, Guilé Jean-Marc, Cohen David, 2019/02/06. Frontiers in Psychiatry, 10.
 
School achievement of deaf children ten years after cochlear implantation
Diaz Lautaro, Labrell Florence, Le Normand Marie-Thérèse, Guinchat Vincent, Dellatolas Georges, 2019/01. Neuropsychiatrie de l'Enfance et de l'Adolescence, 67 (1) pp. 50-57.
 
Équipements de protection individuelle et outils de sécurisation alternatifs à la contention dans la prise en charge des troubles graves du comportement des personnes avec autisme et déficience intellectuelle (partie 1 : perspective des patients)
Lefèvre-Utile J., Guinchat V., Wachtel L.E., Cohen D., Perron A., Montreuil M., Carnevale F.A., Reyre A., 2018/11. Neuropsychiatrie de l'Enfance et de l'Adolescence, 66 (7-8) pp. 443-459.
 
Gestion de la violence : Un dispositif innovant auprès de personnes autistes
Diaz Lautaro, Guinchat Vincent, Lorilleux Alexandra, Alati Julie, Lefèvre-Utile Jean, 2018/05/23. Le Journal des psychologues, n° 358 (6) pp. 20-26.
 
Ehlers-Danlos Syndrome (EDS) - Contribution to Clinical Diagnosis - A Prospective Study of 853 Patients
Hamonet C., Brissot R., Anne Gompel A., Baeza-Velasco C., Guinchat V., Brock I., Ducret L., Pommeret S., Metlaine A., 2018/05/11. EC Neurology, 10 (6) pp. 428-439.
 
Autism, Joint Hypermobility-Related Disorders and Pain.
Baeza-Velasco C., Cohen D., Hamonet C., Vlamynck E., Diaz L., Cravero C., Cappe E., Guinchat V., 2018. Frontiers in psychiatry, 9 p. 656. Peer-reviewed.
 
Ehlers-Danlos Syndrome (EDS) a Diagnostic Trap for the Neurologist, an Iatrogenic Risk for the Patient
Hamonet C., Fred D., Tanay-Marié -, Ducret L., Bahloul H., Guinchat V., Schatz PM, 2017/07/18. EC Neurology, 7 (2) pp. 46-53.
 
Traitements médicamenteux reçus par les enfants, adolescents et jeunes adultes avec trouble du spectre autistique en France : un état des lieux basé sur l'expérience parentale
Cravero C., Guinchat V., Claret-Tournier A., Sahnoun C., Bonniau B., Bodeau N., Danion-Grilliat A., Cohen D., Chamak B., 2017/02. Neuropsychiatrie de l'Enfance et de l'Adolescence, 65 (1) pp. 33-41.
 
Management of Severe Developmental Regression in an Autistic Child with a 1q21.3 Microdeletion and Self-Injurious Blindness
Cravero Cora, Guinchat Vincent, Xavier Jean, Meunier Camille, Diaz Lautaro, Mignot Cyril, Doummar Diane, Chantot-Bastaraud Sandra, Consoli Angèle, Cohen David, 2017. Case Reports in Psychiatry, 2017 pp. 1-8.
 
Nouvelles perspectives ouvertes par les neurosciences dans l’abord des troubles psycho-comportementaux du sujet cérèbrolesé : que signifie l’association entre autisme et paralysie-cérèbrale ?
Guinchat Vincent, Cohen David, Xavier Jean, 2017. pp. 261-282 dans La personne polyhandicapée: la connaître, l'accompagner, la soigner chap. 12, Dunod.
 
Progression of Autism in a Young Woman with CHARGE Syndrome: A Longitudinal Follow-up from Birth
Hamiaux Priscilla, Xavier Jean, Lasserre Elisabeth, Perisse Didier, Baudelaire Karine, Guinchat Vincent, Cohen David, Vaivre Douret Laurence, Abadie Veronique, 2017. International Journal of Mental Health & Psychiatry, 03 (04).
 
Genetic and functional analyses demonstrate a role for abnormal glycinergic signaling in autism.
Pilorge M., Fassier C., Le Corronc H., Potey A., Bai J., De Gois S., Delaby E., Assouline B., Guinchat V., Devillard F. et al., 2016/07. Molecular psychiatry, 21 (7) pp. 936-945. Peer-reviewed.
 
Cornelia de Lange and Ehlers-Danlos: comorbidity of two rare syndromes.
Cravero C., Guinchat V., Barete S., Consoli A., 2016/02/01. BMJ case reports, 2016. Peer-reviewed.
 
Intérêt des unités neurocomportementales multidisciplinaires dans la prise en charge des décompensations aiguës des patients présentant un trouble du spectre autistique
Guinchat V., Cravero C., Diaz L., Assouline M., Lazartigues A., Fiard D., Cohen D., Consoli A., 2015/10. Neuropsychiatrie de l'Enfance et de l'Adolescence, 63 (6) pp. 351-361.
 
Acute behavioral crises in psychiatric inpatients with autism spectrum disorder (ASD): recognition of concomitant medical or non-ASD psychiatric conditions predicts enhanced improvement.
Guinchat V., Cravero C., Diaz L., Périsse D., Xavier J., Amiet C., Gourfinkel-An I., Bodeau N., Wachtel L., Cohen D. et al., 2015/03. Research in developmental disabilities, 38 pp. 242-255. Peer-reviewed.
 
Gene × Environment interactions in autism spectrum disorders: role of epigenetic mechanisms.
Tordjman S., Somogyi E., Coulon N., Kermarrec S., Cohen D., Bronsard G., Bonnot O., Weismann-Arcache C., Botbol M., Lauth B. et al., 2014. Frontiers in psychiatry, 5 p. 53. Peer-reviewed.
 
Signes précoces d'autisme : d'où vient-on ? Où va-t-on ?
Saint-Georges C., Guinchat V., Chamak B., Apicella F., Muratori F., Cohen D., 2013/10. Neuropsychiatrie de l'Enfance et de l'Adolescence, 61 (7-8) pp. 400-408.
 
Electroconvulsive therapy in adolescents with intellectual disability and severe self-injurious behavior and aggression: a retrospective study.
Consoli A., Cohen J., Bodeau N., Guinchat V., Wachtel L., Cohen D., 2013/01. European child & adolescent psychiatry, 22 (1) pp. 55-62. Peer-reviewed.
 
Very early signs of autism reported by parents include many concerns not specific to autism criteria
Guinchat Vincent, Chamak Brigitte, Bonniau Beatrice, Bodeau Nicolas, Perisse Didier, Cohen David, Danion Anne, 2012/04. Research in Autism Spectrum Disorders, 6 (2) pp. 589-601.
 
Pre-, peri- and neonatal risk factors for autism.
Guinchat V., Thorsen P., Laurent C., Cans C., Bodeau N., Cohen D., 2012/03. Acta obstetricia et gynecologica Scandinavica, 91 (3) pp. 287-300. Peer-reviewed.
 
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders.
Leblond C.S., Heinrich J., Delorme R., Proepper C., Betancur C., Huguet G., Konyukh M., Chaste P., Ey E., Rastam M. et al., 2012/02. PLoS genetics, 8 (2) pp. e1002521. Peer-reviewed.
 
Traitement pharmacologique des comportements problématiques associés aux troubles du spectre autistique : revue de la littérature
Périsse D., Guinchat V., Hellings J.A., Baghdadli A., 2012/01. Neuropsychiatrie de l'Enfance et de l'Adolescence, 60 (1) pp. 42-51.
 
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 A.C., Gruchy N., Guillem P., Nguyen Morel M.A., Leporrier N., Leboyer M., Jouk P.S. et al., 2010/09. American journal of medical genetics. Part A, 152A (9) pp. 2346-2354. Peer-reviewed.
 
Risk factors of acute behavioral regression in psychiatrically hospitalized adolescents with autism.
Périsse D., Amiet C., Consoli A., Thorel M.V., Gourfinkel-An I., Bodeau N., Guinchat V., Barthélémy C., Cohen D., 2010/05. Journal of the Canadian Academy of Child and Adolescent Psychiatry = Journal de l'Academie canadienne de psychiatrie de l'enfant et de l'adolescent, 19 (2) pp. 100-108. Peer-reviewed.
 
Trends, perinatal characteristics, and medical conditions in pervasive developmental disorders.
Guillem P., Cans C., Guinchat V., Ratel M., Jouk P.S., 2006/11. Developmental medicine and child neurology, 48 (11) pp. 896-900. Peer-reviewed.
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