Risultati della ricerca - Scheid, Isabelle
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HLA-class II haplotypes and Autism Spectrum Disorders di Bennabi, Meriem, Gaman, Alexandru, Delorme, Richard, Boukouaci, Wahid, Manier, Céline, Scheid, Isabelle, Si Mohammed, Nassima, Bengoufa, Djaouida, Charron, Dominique, Krishnamoorthy, Rajagopal, Leboyer, Marion, Tamouza, Ryad
Pubblicazione 2018testo -
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Clinical and autoimmune features of a patient with autism spectrum disorder seropositive for anti—NMDA-receptor autoantibody di Gréa, Hélène, Scheid, Isabelle, Gaman, Alexandru, Rogemond, Véronique, Gillet, Sandy, Honnorat, Jérôme, Bolognani, Federico, Czech, Christian, Bouquet, Céline, Toledano, Elie, Bouvard, Manuel, Delorme, Richard, Groc, Laurent, Leboyer, Marion
Pubblicazione 2017testo -
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Mutation screening of NOS1AP gene in a large sample of psychiatric patients and controls di Delorme, Richard, Betancur, Catalina, Scheid, Isabelle, Anckarsäter, Henrik, Chaste, Pauline, Jamain, Stéphane, Schuroff, Franck, Nygren, Gudrun, Herbrecht, Evelyn, Dumaine, Anne, Mouren, Marie Christine, Råstam, Maria, Leboyer, Marion, Gillberg, Christopher, Bourgeron, Thomas
Pubblicazione 2010testo -
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Persistence of dysfunctional natural killer cells in adults with high-functioning autism spectrum disorders: stigma/consequence of unresolved early infectious events? di Bennabi, Meriem, Tarantino, Nadine, Gaman, Alexandru, Scheid, Isabelle, Krishnamoorthy, Rajagopal, Debré, Patrice, Bouleau, Arthur, Caralp, Mireille, Gueguen, Sonia, Le-Moal, Myriam Ly, Bouvard, Manuel, Amestoy, Anouck, Delorme, Richard, Leboyer, Marion, Tamouza, Ryad, Vieillard, Vincent
Pubblicazione 2019testo -
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“Reading the Mind in the Eyes” in Autistic Adults is Modulated by Valence and Difficulty: An InFoR Study di Baltazar, Matias, Geoffray, Marie‐Maude, Chatham, Christopher, Bouvard, Manuel, Martinez Teruel, Axelle, Monnet, David, Scheid, Isabelle, Murzi, Eleonora, Couffin‐Cadiergues, Sandrine, Umbricht, Daniel, Murtagh, Lorraine, Delorme, Richard, Ly Le‐Moal, Myriam, Leboyer, Marion, Amestoy, Anouck
Pubblicazione 2020testo -
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Heterozygous FA2H mutations in autism spectrum disorders di Scheid, Isabelle, Maruani, Anna, Huguet, Guillaume, Leblond, Claire S, Nygren, Gudrun, Anckarsäter, Henrik, Beggiato, Anita, Rastam, Maria, Amsellem, Fréderique, Gillberg, I Carina, Elmaleh, Monique, Leboyer, Marion, Gillberg, Christopher, Betancur, Catalina, Coleman, Mary, Hama, Hiroko, Cook, Edwin H, Bourgeron, Thomas, Delorme, Richard
Pubblicazione 2013testo -
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Cerebellar anatomical alterations and attention to eyes in autism di Laidi, Charles, Boisgontier, Jennifer, Chakravarty, M. Mallar, Hotier, Sevan, d’Albis, Marc-Antoine, Mangin, Jean-François, Devenyi, Gabriel A., Delorme, Richard, Bolognani, Federico, Czech, Christian, Bouquet, Céline, Toledano, Elie, Bouvard, Manuel, Gras, Doriane, Petit, Julie, Mishchenko, Marina, Gaman, Alexandru, Scheid, Isabelle, Leboyer, Marion, Zalla, Tiziana, Houenou, Josselin
Pubblicazione 2017testo -
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Identification of Pathway-Biased and Deleterious Melatonin Receptor Mutants in Autism Spectrum Disorders and in the General Population di Chaste, Pauline, Clement, Nathalie, Mercati, Oriane, Guillaume, Jean-Luc, Delorme, Richard, Botros, Hany Goubran, Pagan, Cécile, Périvier, Samuel, Scheid, Isabelle, Nygren, Gudrun, Anckarsäter, Henrik, Rastam, Maria, Ståhlberg, Ola, Gillberg, Carina, Serrano, Emilie, Lemière, Nathalie, Launay, Jean Marie, Mouren-Simeoni, Marie Christine, Leboyer, Marion, Gillberg, Christopher, Jockers, Ralf, Bourgeron, Thomas
Pubblicazione 2010testo