Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Moise Assouline"'
Autor:
Jean-Pierre Malen, Moise Assouline, Caroline Demily, Gilles Roland-Manuel, Claude Besmond, Lisa Frugère, Emeline Throo, Laurence Hubert, Mélanie Ferreri, Sylvain Hanein, Valérie Malan, Nathalie Boddaert, Céline Vidal, Charlyne Duwime, Giulia Barcia, Arnold Munnich
Publikováno v:
médecine/sciences. 35:843-851
Malgré les avancées de la recherche, un grand nombre de patients atteints de troubles du spectre autistique (TSA) n’ont pas accès aux explorations aujourd’hui disponibles, du fait d’idées reçues, de l’insuffisance des structures à
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f33686ec008f068c744b73e3ee67fb8c
https://doi.org/10.1051/medsci/2019170
https://doi.org/10.1051/medsci/2019170
Autor:
Caroline Demily, Emeline Throo, Mélanie Ferreri, Laurence Hubert, Nathalie Boddaert, Lisa Frugère, Sylvain Hanein, Valérie Malan, Arnold Munnich, Jean-Christophe Thalabard, Jean-Pierre Malen, Claude Besmond, Charlyne Duwime, Céline Vidal, Gilles Roland-Manuel, Moise Assouline, Giulia Barcia
Publikováno v:
Molecular Autism, Vol 10, Iss 1, Pp 1-10 (2019)
Molecular Autism
Molecular Autism
Background Neurogenetics investigations and diagnostic yield in patients with autism spectrum disorder (ASD) have significantly improved over the last few years. Yet, many patients still fail to be systematically investigated. Methods To improve acce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e348a07b85cf1900983fdc7e79f13b26
http://link.springer.com/article/10.1186/s13229-019-0284-2
http://link.springer.com/article/10.1186/s13229-019-0284-2
Autor:
Arnold Munnich, Caroline Demily, Lisa Frugère, Charlyne Duwime, Valérie Malan, Giulia Barcia, Céline Vidal, Emeline Throo, Claude Besmond, Laurence Hubert, Gilles Roland-Manuel, Jean-Pierre Malen, Mélanie Ferreri, Sylvain Hanein, Jean-Christophe Thalabard, Nathalie Boddaert, Moïse Assouline
Publikováno v:
Molecular Autism, Vol 10, Iss 1, Pp 1-10 (2019)
Abstract Background Neurogenetics investigations and diagnostic yield in patients with autism spectrum disorder (ASD) have significantly improved over the last few years. Yet, many patients still fail to be systematically investigated. Methods To imp
Externí odkaz:
https://doaj.org/article/82edb3badd9e428b9096501733b083a1