Weight loss induced by quetiapine in a 22q11.2DS patient

por Demily, Caroline, Poisson, Alice, Thibaut, Florence, Franck, Nicolas
Publicado no Mol Genet Metab Rep (2017)

Low dose clozapine controls adult-onset psychosis associated with the neurogenic ataxia-retinitis pigmentosa (NARP) mutation

por Demily, Caroline, Duwime, Charlyne, Poisson, Alice, Boddaert, Nathalie, Munnich, Arnold
Publicado no Mol Genet Metab Rep (2016)

Authors' reply — Clozapine for mitochondrial psychosis

por Demily, Caroline, Duwime, Charlyne, Poisson, Alice, Boddaert, Nathalie, Munnich, Arnold
Publicado no Mol Genet Metab Rep (2017)

Computer-based cognitive remediation program for the treatment of behavioral problems in children with intellectual disability: the «COGNITUS & MOI» study protocol for a randomized...

por Favre, Emilie, Peyroux, Elodie, Babinet, Marie-Noelle, Poisson, Alice, Demily, Caroline
Publicado no BMC Psychiatry (2018)

Impaired neural processing of transitive relations in children with math learning difficulty

por Schwartz, Flora, Epinat-Duclos, Justine, Léone, Jessica, Poisson, Alice, Prado, Jérôme
Publicado no Neuroimage Clin (2018)

The Almirall European Headache Awards 2009

por Grimaldi, Daniela, Batista, Sónia, Poisson, Alice, Verschelde, Hanne-Laure, Vázquez-Sánchez, Fernando
Publicado em 2010

Smith-Magenis Syndrome: Molecular Basis of a Genetic-Driven Melatonin Circadian Secretion Disorder

por Poisson, Alice, Nicolas, Alain, Bousquet, Idriss, Raverot, Véronique, Gronfier, Claude, Demily, Caroline
Publicado no Int J Mol Sci (2019)

Complex phenotype with social communication disorder caused by mosaic supernumerary ring chromosome 19p

por Demily, Caroline, Rossi, Massimiliano, Chesnoy-Servanin, Gabrielle, Martin, Brice, Poisson, Alice, Sanlaville, Damien, Edery, Patrick
Publicado no BMC Med Genet (2014)

Autism spectrum disorder associated with 49,XYYYY: case report and review of the literature

por Demily, Caroline, Poisson, Alice, Peyroux, Elodie, Gatellier, Valérie, Nicolas, Alain, Rigard, Caroline, Schluth-Bolard, Caroline, Sanlaville, Damien, Rossi, Massimiliano
Publicado no BMC Med Genet (2017)

Chromatin remodeling dysfunction extends the etiological spectrum of schizophrenia: a case report

por Poisson, Alice, Chatron, Nicolas, Labalme, Audrey, Fourneret, Pierre, Ville, Dorothée, Mathieu, Marie Laure, Sanlaville, Damien, Demily, Caroline, Lesca, Gaëtan
Publicado no BMC Med Genet (2020)

Erotomania and phenotypic continuum in a family frameshift variant of AUTS2: a case report and review

por GAULD, Christophe, POISSON, Alice, REVERSAT, Julie, PEYROUX, Elodie, HOUDAYER-ROBERT, Françoise, ROSSI, Massimiliano, LESCA, Gaetan, SANLAVILLE, Damien, DEMILY, Caroline
Publicado no BMC Psychiatry (2021)

A Functional Magnetic Resonance Imaging Study of Pathophysiological Changes Responsible for Mirror Movements in Parkinson’s Disease

por Poisson, Alice, Ballanger, Bénédicte, Metereau, Elise, Redouté, Jérome, Ibarolla, Danielle, Comte, Jean-Christophe, Bernard, Hélène Gervais, Vidailhet, Marie, Broussolle, Emmanuel, Thobois, Stéphane
Publicado em 2013

Behavioral disturbance and treatment strategies in Smith-Magenis syndrome

por Poisson, Alice, Nicolas, Alain, Cochat, Pierre, Sanlaville, Damien, Rigard, Caroline, de Leersnyder, Hélène, Franco, Patricia, Portes, Vincent Des, Edery, Patrick, Demily, Caroline
Publicado no Orphanet J Rare Dis (2015)