Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Gabrielle Allio"'
Publikováno v:
Cliniques. :83-98
Autor:
Gabrielle Allio, Mathieu Follet, Xavier Lemoine, Marie Desbordes, Michel Petit, Féthi Brétel, Sadeq Haouzir
Publikováno v:
Annales Médico-psychologiques, revue psychiatrique. 173:908-912
Resume Nous rapportons ici le cas d’une femme âgee de 60 ans presentant un trouble « thymique » difficilement categorisable, et qui est l’occasion d’une reflexion theorique et physiopathologique sur certains aspects de la classification des
Autor:
Florence Thibaut, Mohamed Rebaï, Gabrielle Allio, Gaël Fouldrin, Robert Lalonde, Michel Petit, Carole Di Maggio-Clozel, Sadec Haouzir, Christian Bernard, Stéphanie Caharel
Publikováno v:
Schizophrenia Research. 95:186-196
Background The main objective of the study was to determine whether patients with schizophrenia are deficient relative to controls in the processing of faces at different levels of familiarity and types of emotion and the stage where such differences
Autor:
Gabrielle Allio, Dominique Campion, Florence Thibaut, D. Levillain, Sandrine Louchart-de la Chapelle, Sadeq Haouzir, Sonia Dollfus, Alexis Van Der Elst, Jean-François Ménard
Publikováno v:
Psychiatry Research. 136:27-34
Abnormal sensory gating in schizophrenia has frequently been reported. The strength of central inhibitory pathways was measured using the P50 component of the auditory evoked potential in a conditioning-testing paradigm. The relationships between a r
Autor:
Caroline Demily, A Tillaux, Thierry Frebourg, Michel Petit, Sonia Dollfus, Dominique Campion, Jean-François Ménard, J Lerond, G Raux, C Bellegou, Hélène Jacquet, Gabrielle Allio, Florence Thibaut, Emmanuelle Houy, Pascal Delamillieure, Sadeq Haouzir, Gaël Fouldrin, Jacqueline Bou, Thierry d'Amato, Bernadette Hecketsweiler
Publikováno v:
Molecular Psychiatry. 10:479-485
DNA sequence variations within the 22q11 DiGeorge chromosomal region are likely to confer susceptibility to psychotic disorders. In a previous report, we identified several heterozygous alterations, including a complete deletion, of the proline dehyd
Autor:
Dominique Campion, Florence Thibaut, Michel Petit, Frédérique Bonnet-Brilhault, Emmanuelle Houy, G Raux, Gabrielle Allio, Maria Martinez, Thierry Frebourg, Sadeq Haouzir, S. Louchart, D. Levillain, R. Gantier
Publikováno v:
Molecular Psychiatry. 7:1006-1011
Abnormality in the P50 auditory-evoked potential gating is an endophenotype associated with schizophrenia. Biochemical and genetic studies have suggested that the alpha 7 nicotinic acetylcholine receptor (nAChR) is involved in this sensory gating def
Autor:
Caroline Demily, Dominique Campion, Sadeq Haouzir, Thierry Frebourg, A Belmont, Gaël Fouldrin, Emmanuelle Houy, G Raux, Michel Petit, Gabrielle Allio, Florence Thibaut
Publikováno v:
Molecular Psychiatry. 9:320-322
As suggested by several studies, abnormal sensory gating measured by the P50 paradigm could be an endophenotype predisposing to schizophrenia. In a previous work, we have shown a significant association between the presence of at least one −2 bp de
Autor:
Laurence Briant, Freddy Jouen, Marie Desbordes, Mathieu Follet, Xavier Lemoine, Zohra Baarir, Michel Petit, Sadeq Haouzir, Claire Meunier, Jean-François Ménard, Gabrielle Allio
Publikováno v:
Psychiatry Research
Psychiatry Research, Elsevier, 2009, 168 (1), pp.78-85
Psychiatry Research, Elsevier, 2009, 168 (1), pp.78-85
Catatonia is a common but under-diagnosed neuropsychiatric syndrome characterized by the occurrence in a single patient of concomitant affective, motor and behavioral symptoms with a hazardous outcome (called lethal catatonia: LC). Deaths by thromboe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5e89db77814eed4b4cd9ce800f83727
https://hal.archives-ouvertes.fr/hal-00486216
https://hal.archives-ouvertes.fr/hal-00486216
Autor:
Florence Thibaut, Solenn Legallic, Jacqueline Bou, Thierry Frebourg, Michel Petit, Gabrielle Allio, Dominique Campion, Sadeq Haouzir, Caroline Demily
Publikováno v:
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics. (1)
A translocation disrupting the DISC 1 gene segregates with schizophrenia and related psychiatric disorders in a large Scottish family. Mutation screening of this gene by routine PCR-based methods has remained largely negative. We sought to detect rea
Autor:
Thierry Frebourg, G Raux, Caroline Demilly, Hélène Jacquet, Gabrielle Allio, Florence Thibaut, Gaël Fouldrin, Emmanuelle Houy, Bernadette Hecketsweiler, Valérie Drouin, Michel Petit, Jacqueline Bou, Dominique Campion, Sadeq Haouzir
Publikováno v:
Human molecular genetics. 11(19)
The increased prevalence of schizophrenia among patients with the 22q11 interstitial deletion associated with DiGeorge syndrome has suggested the existence of a susceptibility gene for schizophrenia within the DiGeorge syndrome chromosomal region (DG