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收藏Economic analysis of early intervention for autistic children: findings from four case studies in England, Ireland, Italy, and Spain自闭症儿童早期干预的经济分析: 来自英格兰，爱尔兰，意大利和西班牙的四个案例研究的结果
Tinelli, Michela; Roddy, Aine; Knapp, Martin; Arango, Celso; Mendez, Maria Andreina; Cusack, James; Murphy, Declan; Canitano, Roberto; Oakley, Bethany; Quoidbach, Vinciane 分享 收藏 Autism care pathway in Europe欧洲的自闭症护理路径Mendez, Maria A.; Oakley, Bethany; Canitano, Roberto; San Jose-Caceres, Antonia; Tinelli, Michela; Knapp, Martin; Cusack, James; Parellada, Mara; Violland, Pierre; Plas, Jan R. Derk; Canal-Bedia, Ricardo; Bejarano-Martin, Alvaro; Murphy, Declan G. M.; Quoidbach, Vinciane; Arango, Celso 分享 收藏 Autism with co-occurring epilepsy care pathway in EuropeMendez, Maria A.; Canitano, Roberto; Oakley, Bethany; San Jose-Caceres, Antonia; Tinelli, Michela; Knapp, Martin; Cusack, James; Parellada, Mara; Violland, Pierre; Plas, Jan Derk R.; Murphy, Declan G. M.; Quoidbach, Vinciane; Arango, Celso 分享 收藏 Economic Evaluation of anti-epileptic Medicines for Autistic Children with EpilepsyTinelli, Michela M.; Roddy, Aine; Knapp, Martin; Arango, Celso; Mendez, Maria Andreina; Cusack, James; Murphy, Declan; Canitano, Roberto; Oakley, Bethany; Quoidbach, Vinciane 分享 收藏 Natural history of KBG syndrome in a large European cohort大型欧洲队列中KBG综合征的自然史Loberti, Lorenzo; Bruno, Lucia Pia; Granata, Stefania; Doddato, Gabriella; Resciniti, Sara; Fava, Francesca; Carullo, Michele; Rahikkala, Elisa; Jouret, Guillaume; Menke, Leonie A.; Lederer, Damien; Vrielynck, Pascal; Ryba, Lukas; Brunetti-Pierri, Nicola; Lasa-Aranzasti, Amaia; Cueto-Gonzalez, Anna Maria; Trujillano, Laura; Valenzuela, Irene; Tizzano, Eduardo F.; Spinelli, Alessandro Mauro; Bruno, Irene; Curro, Aurora; Stanzial, Franco; Benedicenti, Francesco; Lopergolo, Diego; Santorelli, Filippo Maria; Aristidou, Constantia; Tanteles, George A.; Maystadt, Isabelle; Tkemaladze, Tinatin; Reimand, Tiia; Lokke, Helen; Ounap, Katrin; Haanpaa, Maria K.; Holubova, Andrea; Zoubkova, Veronika; Schwarz, Martin; Zordania, Riina; Muru, Kai; Roht, Laura; Tihverainen, Annika; Teek, Rita; Thomson, Ulvi; Isis, Atallah; Superti-Furga, Andrea; Buoni, Sabrina; Canitano, Roberto; Scandurra, Valeria; Rossetti, Annalisa; Grosso, Salvatore; Battini, Roberta; Baldassarri, Margherita; Mencarelli, Maria Antonietta; Lo Rizzo, Caterina; Bruttini, Mirella; Mari, Francesca; Ariani, Francesca; Renieri, Alessandra; Maria, Anna 分享 收藏 分享 收藏 Identification of a Novel Pathogenic Variant in the NAGLU Gene in a Child with Neurodevelopmental DelayBruno, Lucia Pia; Fava, Francesca; Baldassarri, Margherita; Salvati, Virginia M.; Scandurra, Valeria; Canitano, Roberto; Valentino, Floriana; Doddato, Gabriella; Tita, Rossella; Giliberti, Annarita; Renieri, Alessandra; Ariani, Francesca 分享 收藏 Variants in the SK2 channel gene (KCNN2) lead to dominant neurodevelopmental movement disordersMochel, Fanny; Rastetter, Agnes; Ceulemans, Berten; Platzer, Konrad; Yang, Sandra; Shinde, Deepali N.; Helbig, Katherine L.; Lopergolo, Diego; Mari, Francesca; Renieri, Alessandra; Benetti, Elisa; Canitano, Roberto; Waisfisz, Quinten; Plomp, Astrid S.; Huisman, Sylvia A.; Wilson, Golder N.; Cathey, Sara S.; Louie, Raymond J.; Del Gaudio, Daniela; Waggoner, Darrel; Kacker, Shawn; Nugent, Kimberly M.; Roeder, Elizabeth R.; Bruel, Ange-Line; Thevenon, Julien; Ehmke, Nadja; Horn, Denise; Holtgrewe, Manuel; Kaiser, Frank J.; Kamphausen, Susanne B.; Abou Jamra, Rami; Weckhuysen, Sarah; Dalle, Carine; Depienne, Christel 分享 收藏 分享 收藏 分享 收藏 分享 收藏 分享 收藏 Evaluating Sex and Age Differences in ADI-R and ADOS Scores in a Large European Multi-site Sample of Individuals with Autism Spectrum DisorderTillmann, J.; Ashwood, K.; Absoud, M.; Bolte, S.; Bonnet-Brilhault, F.; Buitelaar, J. K.; Calderoni, S.; Calvo, R.; Canal-Bedia, R.; Canitano, R.; De Bildt, A.; Gomot, M.; Hoekstra, P. J.; Kaale, A.; McConachie, H.; Murphy, D. G.; Narzisi, A.; Oosterling, I.; Pejovic-Milovancevic, M.; Persico, A. M.; Puig, O.; Roeyers, H.; Rommelse, N.; Sacco, R.; Scandurra, V.; Stanfield, A. C.; Zander, E.; Charman, T. 分享 收藏 分享 收藏 分享 收藏 分享 收藏 Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiencySoorya, Latha; Kolevzon, Alexander; Zweifach, Jessica; Lim, Teresa; Dobry, Yuriy; Schwartz, Lily; Frank, Yitzchak; Wang, A. Ting; Cai, Guiqing; Parkhomenko, Elena; Halpern, Danielle; Grodberg, David; Angarita, Benjamin; Willner, Judith P.; Yang, Amy; Canitano, Roberto; Chaplin, William; Betancur, Catalina; Buxbaum, Joseph D. 分享 收藏 Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorderNewbury, Dianne F.; Mari, Francesca; Akha, Elham Sadighi; MacDermot, Kay D.; Canitano, Roberto; Monaco, Anthony P.; Taylor, Jenny C.; Renieri, Alessandra; Fisher, Simon E.; Knight, Samantha J. L. 分享 收藏 分享 收藏 
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