Zobrazeno 1 - 10
of 124
pro vyhledávání: '"CHASTE, Pauline"'
Publikováno v:
In Journal of Psychiatric Research October 2024 178:88-93
Autor:
Lefèvre, Hervé, Stheneur, Chantal, Cardin, Charlotte, Fourcade, Lola, Fourmaux, Christine, Tordjman, Elise, Touati, Marie, Voisard, Flore, Minassian, Sevan, Chaste, Pauline, Moro, Marie Rose, Lachal, Jonathan
Publikováno v:
In Journal of Pain and Symptom Management February 2021 61(2):416-422
Autor:
Zalla, Tiziana, Sirigu, Angela, Robic, Suzanne, Chaste, Pauline, Leboyer, Marion, Coricelli, Giorgio
Publikováno v:
In Cortex September 2014 58:112-122
Autor:
Chaput, Valérie, Amsellem, Frédérique, Urdapilleta, Isabel, Chaste, Pauline, Leboyer, Marion, Delorme, Richard, Goussé, Véronique
Publikováno v:
In Research in Autism Spectrum Disorders September 2013 7(9):1062-1067
Akademický článek
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Autor:
Chaste, Pauline, Clement, Nathalie, Botros, Hany, Guillaume, Jean-Luc, Konyukh, Marina, Pagan, Cécile, Scheid, Isabelle, Nygren, Gudrun, Anckarsäter, Henrik, Råstam, Maria, Ståhlberg, Ola, Gillberg, I. Carina, Melke, Jonas, Delorme, Richard, Leblond, Claire, Toro, Roberto, Huguet, Guillaume, Fauchereau, Fabien, Durand, Christelle, Boudarene, Lydia, Serrano, Emilie, Lemière, Nathalie, Launay, Jean Marie, Leboyer, Marion, Jockers, Ralf, Gillberg, Christopher, Bourgeron, Thomas
Sleep wake cycles are frequently disturbed in patients with Attention Deficit and Hyperactivity Disorders. We hypothesized that the origin of the sleep problems may be the consequence of an abnormal circadian clock setting regulated by the melatonin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::6e5c17c22879f57067b6485f03384a72
https://hal-pasteur.archives-ouvertes.fr/pasteur-01967147
https://hal-pasteur.archives-ouvertes.fr/pasteur-01967147
Autor:
Klei Lambertus, Sanders Stephan J, Murtha Michael T, Hus Vanessa, Lowe Jennifer K, Willsey A, Moreno-De-Luca Daniel, Yu Timothy W, Fombonne Eric, Geschwind Daniel, Grice Dorothy E, Ledbetter David H, Lord Catherine, Mane Shrikant M, Martin Christa, Martin Donna M, Morrow Eric M, Walsh Christopher A, Melhem Nadine M, Chaste Pauline, Sutcliffe James S, State Matthew W, Cook Edwin H, Roeder Kathryn, Devlin Bernie
Publikováno v:
Molecular Autism, Vol 3, Iss 1, p 9 (2012)
Abstract Background Autism spectrum disorders (ASD) are early onset neurodevelopmental syndromes typified by impairments in reciprocal social interaction and communication, accompanied by restricted and repetitive behaviors. While rare and especially
Externí odkaz:
https://doaj.org/article/e00a785ffaf64e9a812e2922484cd74e
Autor:
Chaste Pauline, Betancur Catalina, Gérard-Blanluet Marion, Bargiacchi Anne, Kuzbari Suzanne, Drunat Séverine, Leboyer Marion, Bourgeron Thomas, Delorme Richard
Publikováno v:
Molecular Autism, Vol 3, Iss 1, p 5 (2012)
Abstract Background Fragile X syndrome (FXS) is the most common inherited cause of intellectual disability (ID), as well as the most frequent monogenic cause of autism spectrum disorder (ASD). Men with FXS exhibit ID, often associated with autistics
Externí odkaz:
https://doaj.org/article/fb5293118c9d410c82735dac372d4d90
Autor:
Nygren Gudrun, Schuroff Franck, Jamain Stéphane, Chaste Pauline, Anckarsäter Henrik, Scheid Isabelle, Betancur Catalina, Delorme Richard, Herbrecht Evelyn, Dumaine Anne, Mouren Marie, Råstam Maria, Leboyer Marion, Gillberg Christopher, Bourgeron Thomas
Publikováno v:
BMC Medical Genetics, Vol 11, Iss 1, p 108 (2010)
Abstract Background The gene encoding carboxyl-terminal PDZ ligand of neuronal nitric oxide synthase (NOS1AP) is located on chromosome 1q23.3, a candidate region for schizophrenia, autism spectrum disorders (ASD) and obsessive-compulsive disorder (OC
Externí odkaz:
https://doaj.org/article/31eebaf8aa1d456ab3947ef4484e77b8
Autor:
Grabe Hans, Mössner Rainald, Chaste Pauline, Maier Wolfgang, Gennetier Aurélie, Moreno-De-Luca Daniel, Delorme Richard, Ruhrmann Stephan, Falkai Peter, Mouren Marie-Christine, Leboyer Marion, Wagner Michael, Betancur Catalina
Publikováno v:
BMC Medical Genetics, Vol 11, Iss 1, p 100 (2010)
Abstract Background Obsessive-compulsive disorder (OCD) is a clinically and etiologically heterogeneous syndrome. The high frequency of obsessive-compulsive symptoms reported in subjects with the 22q11.2 deletion syndrome (DiGeorge/velocardiofacial s
Externí odkaz:
https://doaj.org/article/6e8f05b21cb1452e925a22a730ad136d