Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Sarah Menghetti"'
Autor:
Alexandra Zaharia, Maude Schneider, Bronwyn Glaser, Martina Franchini, Sarah Menghetti, Marie Schaer, Martin Debbané, Stephan Eliez
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 10, Iss 1, Pp 1-14 (2018)
Abstract Background Previous research links social difficulties to atypical face exploration in 22q11.2 deletion syndrome (22q11.2DS). Two types of face processing are distinguished: configural (CFP) and featural (FFP). CFP develops later in life and
Externí odkaz:
https://doaj.org/article/006f509b14b84ab0acf9c006e51ec4a0
Autor:
Miralena I. Tomescu, Tonia A. Rihs, Maya Roinishvili, F. Isik Karahanoglu, Maude Schneider, Sarah Menghetti, Dimitri Van De Ville, Andreas Brand, Eka Chkonia, Stephan Eliez, Michael H. Herzog, Christoph M. Michel, Céline Cappe
Publikováno v:
Schizophrenia Research: Cognition, Vol 2, Iss 3, Pp 159-165 (2015)
Schizophrenia is a complex psychiatric disorder and many of the factors contributing to its pathogenesis are poorly understood. In addition, identifying reliable neurophysiological markers would improve diagnosis and early identification of this dise
Externí odkaz:
https://doaj.org/article/3664b597d3294e36a9f9e04c43c791d7
Autor:
Deborah Myriam Badoud, Maude Schneider, Martin Debbané, Stephan Eliez, Bronwyn Glaser, Sarah Menghetti
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 9, Iss 1, Pp 1-9 (2017)
Journal of Neurodevelopmental Disorders
Journal of Neurodevelopmental Disorders, Vol. 9, No 1 (2017) P. 35
Journal of Neurodevelopmental Disorders
Journal of Neurodevelopmental Disorders, Vol. 9, No 1 (2017) P. 35
Background Although significant impairments in the affective and cognitive facets of social cognition have been highlighted in patients with 22q11.2 deletion syndrome (22q11DS) in previous studies, these domains have never been investigated simultane
Autor:
Monika Kott-Radecka, Stephan Eliez, M. Debanné, Bronwyn Glaser, David Sander, Sarah Menghetti, Marie Schaer, Maude Schneider, Martina Franchini
Publikováno v:
Journal of Intellectual Disability Research. 60:308-321
Introduction The 22q11.2 deletion syndrome (22q11DS) is a neurogenetic syndrome. Individuals affected by this syndrome present poor social functioning and a high risk for the development of psychiatric disorders. Accurate emotion recognition and visu
Autor:
Stephan Eliez, Alexandra Zaharia, Marie Schaer, Sarah Menghetti, Maude Schneider, Bronwyn Glaser, Martin Debbané, Martina Franchini
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol. 10, No 26 (2018)
Journal of Neurodevelopmental Disorders
Journal of Neurodevelopmental Disorders, Vol 10, Iss 1, Pp 1-14 (2018)
Journal of Neurodevelopmental Disorders
Journal of Neurodevelopmental Disorders, Vol 10, Iss 1, Pp 1-14 (2018)
BACKGROUND: Previous research links social difficulties to atypical face exploration in 22q11.2 deletion syndrome (22q11.2DS). Two types of face processing are distinguished: configural (CFP) and featural (FFP). CFP develops later in life and plays a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef202607bc95f28026cd96f825079440
https://archive-ouverte.unige.ch/unige:109266
https://archive-ouverte.unige.ch/unige:109266
Autor:
F. Isik Karahanoglu, Stephan Eliez, Christoph M. Michel, Michael H. Herzog, Sarah Menghetti, Céline Cappe, Tonia A. Rihs, Maude Schneider, Miralena I. Tomescu, Maya Roinishvili, Dimitri Van De Ville, Andreas Brand, Eka Chkonia
Publikováno v:
Schizophrenia Research, Vol. 2, No 3 (2015) pp. 159-165
Schizophrenia Research: Cognition, Vol 2, Iss 3, Pp 159-165 (2015)
Schizophrenia Research: Cognition
Schizophrenia Research: Cognition, 2015, 2 (3), pp.159--165. ⟨10.1016/j.scog.2015.04.005⟩
Schizophrenia Research: Cognition, Vol 2, Iss 3, Pp 159-165 (2015)
Schizophrenia Research: Cognition
Schizophrenia Research: Cognition, 2015, 2 (3), pp.159--165. ⟨10.1016/j.scog.2015.04.005⟩
Schizophrenia is a complex psychiatric disorder and many of the factors contributing to its pathogenesis are poorly understood. In addition, identifying reliable neurophysiological markers would improve diagnosis and early identification of this dise
Publikováno v:
Early Intervention in Psychiatry. 11:156-164
22q11.2 deletion syndrome (22q11.2DS) is a neurogenetic condition associated with an increased risk of developing schizophrenia. Previous studies have shown that negative symptoms represent the most specific clinical characteristic of psychosis in 22
Publikováno v:
Early Intervention in Psychiatry, Vol. 11, No 2 (2017) pp. 156-164
Early intervention in psychiatry
Early intervention in psychiatry
AIMS 22q11.2 deletion syndrome (22q11.2DS) is a neurogenetic condition associated with an increased risk of developing schizophrenia. Previous studies have shown that negative symptoms represent the most specific clinical characteristic of psychosis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::3e37d7f06c7a554510ded4c0df696aa6
https://archive-ouverte.unige.ch/unige:55003
https://archive-ouverte.unige.ch/unige:55003
Autor:
Bronwyn Glaser, Martin Debbané, Maude Schneider, Stephan Eliez, A. Kadir Mutlu, Marie Schaer, Sarah Menghetti
Publikováno v:
European Child & Adolescent Psychiatry
European Child and Adolescent Psychiatry, Vol. 23, No 6 (2014) pp. 425-436
European Child and Adolescent Psychiatry
European Child and Adolescent Psychiatry, Vol. 23, No 6 (2014) pp. 425-436
European Child and Adolescent Psychiatry
22q11.2 deletion syndrome (22q11DS) is associated with increased risk for schizophrenia. Better identifying risk factors for the emergence of psychotic symptoms in this population is needed to improve clinical assessment and early interventions. Schi
Autor:
Martin Debbané, Johanna Maeder, Mathilde Bostelmann, Marie Schaer, Stephan Eliez, Sarah Menghetti, Maude Schneider, Bronwyn Glaser
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol. 8, No 1 (2016)
Journal of neurodevelopmental disorders
Journal of Neurodevelopmental Disorders
Journal of neurodevelopmental disorders
Journal of Neurodevelopmental Disorders
Background 22q11.2 deletion syndrome (22q11.2DS) is a genetic disorder associated with a specific cognitive profile. Higher-order cognitive skills like executive functions (EF) are reported as a relative weakness in this population. The present study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43e31c60289ab0e4e06a45ea9a1062a3
https://jneurodevdisorders.biomedcentral.com/articles/10.1186/s11689-016-9141-1
https://jneurodevdisorders.biomedcentral.com/articles/10.1186/s11689-016-9141-1