Kolexia
Coutelle Romain
Psychiatrie
Hôpital Elsau
Strasbourg, France
51 Activités
0 Followers

Scientifique
Digital
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Sujets de recherche
{{person.topmesh1.name}} Déficience intellectuelle COVID-19 Troubles de la mémoire Maladies rares Maladies génétiques congénitales Troubles de la veille et du sommeil Effets différés de l'exposition prénatale à des facteurs de risque Malformations multiples Troubles de l'endormissement et du maintien du sommeil

Industries

Janssen
3 collaboration(s)
Dernière en 2017
Sanofi
1 collaboration(s)
Dernière en 2017
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Dernières activités

Neurocognitive and neurobehavioral characterization of two frequent forms of neurodevelopmental disorders: the DYRK1A and the Wiedemann-Steiner syndromes
Abstracts from the 56th European Society of Human Genetics (ESHG) Conference   01 janvier 2024
Development, psychometric evaluation, and factor analysis of an instrument measuring quality of life in autistic preschoolers.
International journal of methods in psychiatric research   22 décembre 2023
Investigating the borders of autism spectrum disorder: lessons from the former diagnosis of pervasive developmental disorder not otherwise specified.
Frontiers in psychiatry   19 décembre 2023
Psychotherapies in opioid use disorder: toward a step-care model.
Journal of neural transmission (Vienna, Austria : 1996)   21 novembre 2023
Maternal immune activation during pregnancy is associated with more difficulties in socio-adaptive behaviors in autism spectrum disorder.
Scientific reports   17 octobre 2023
Autisemo: Dialectical Behavior Therapy for Adults With Autism Spectrum Disorders Without Intellectual Disability: a Randomized Controlled Trial
Essai Clinique (CHU Strasbourg)   18 août 2023
French Validation of the Camouflaging Autistic Traits Questionnaire (CAT-Q).
Journal of autism and developmental disorders   22 juin 2023
Emotion dysregulation is heightened in autistic females: A comparison with autistic males and borderline personality disorder.
Women's health (London, England)   24 mai 2023
GenIDA, an international participatory database to better understand the natural history and comorbidities of genetic forms of neurodevelopmental disorders
Abstracts from the 55th European Society of Human Genetics (ESHG) Conference   01 mai 2023
Syndrome de Wiedemann-Steiner (WSS)
HAS Publications   13 décembre 2022