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Angèle Consoli

Researcher at Pierre-and-Marie-Curie University

Publications -  75
Citations -  2646

Angèle Consoli is an academic researcher from Pierre-and-Marie-Curie University. The author has contributed to research in topics: Catatonia & Population. The author has an hindex of 25, co-authored 68 publications receiving 1744 citations. Previous affiliations of Angèle Consoli include University of Picardie Jules Verne & Paris Descartes University.

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Facteurs de risque psychosociaux et troubles psychiatriques des jeunes pris en charge par l’aide sociale à l’enfance et ayant recours à des soins hospitaliers

TL;DR: In this article, the authors explore specificities des troubles psychiatriques presentes par les jeunes pris en charge par l'aide sociale a l'enfance (ASE), and des facteurs de risque auxquels ils sont confrontes.
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Borderline personality disorder and prior suicide attempts define a severity gradient among hospitalized adolescent suicide attempters.

TL;DR: Borderline personality disorder (BPD) and history of prior suicide attempt (SA) are examined to improve youth suicide prevention and the efficacy of reinforcing early interventions for anxiety disorders and NSSI.
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Disentangling Tourette syndrome heterogeneity through hierarchical ascendant clustering

TL;DR: To explore the heterogeneity of Tourette syndrome as part of a neurodevelopmental spectrum, a large number of cases are diagnosed with a single underlying condition, namely Tourette's syndrome.
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Troubles bipolaires de type I de l’adolescent : controverses et devenir à l’âge adulte

TL;DR: Ces donnees suggerent que l’examen psychologique associant evaluations cognitive et projective pourrait etre un indice pronostique du risque de transition schizophrenique necessitent souvent une hospitalisation prolongee pour consolider l”amelioration en phase aigue.
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Catatonia in Children and Adolescents: A High Rate of Genetic Conditions.

TL;DR: The first systematic molecular genetic data for this syndrome is reported, among the 89 patients consecutively admitted for catatonia between 1993 and 2014, to identify 51 patients who had genetic laboratory testing and assess the causality of observed genetic findings.