Menke-Hennekam syndrome 1: A Case Report by Trusmei, M., Budisteanu, M.

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Abundant pleiotropy across neuroimaging modalities identified through a multivariate genome-wide association study by Tissink, E. P., Shadrin, A. A., van der Meer, D., Parker, N., Hindley, G., Roelfs, D., Frei, O., Fan, C. C., Nagel, M., Nærland, T., Budisteanu, M., Djurovic, S., Westlye, L. T., van den Heuvel, M. P., Posthuma, D., Kaufmann, T., Dale, A. M., Andreassen, O. A.

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Genomic imbalances of chromosome 15 in patients with autistic features and global developmental delay by Budisteanu, M., Papuc, S., Erbescu, A., Albulescu, L., Arghir, A.

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Multidisciplinary approach in children with autism spectrum disorder by Stanciu, A.C., Rad, F., Mihailescu, I., Mateescu, L., Grozavescu, R., Andrei, E., Budisteanu, B., Linca, F., Ioana, D., Iliescu, C., Papuc, S., Arghir, A., Dobrescu, I., Budisteanu, M.

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The psychiatric phenotype of 15q11.2-q13.3 duplications by Budisteanu, M., Papuc, S., Erbescu, A., Andrei, E., Streata, I., Cucu, M., Iliescu, C., Anghelescu, C., Ioana, D., Ioana, M., Rad, F., Arghir, A.

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Behavior problems associated with brain heterotopia by Budisteanu, M., Papuc, S., Erbescu, A., Iliescu, C., Dobre, M., Barca, D., Tarta-Arsene, O., Motoescu, C., Dica, A., Sandu, C., Anghelescu, C., Craiu, D., Arghir, A.

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Floating-Harbor syndrome: Presentation of the first Romanian patient with a SRCAP mutation and review of the literature by Budisteanu, M, Bögershausen, N, Papuc, SM, Moosa, S, Thoenes, M, Riga, D, Arghir, A, Wollnik, B

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PP11.11 – 2673: Phelan-McDermid syndrome in two siblings with complex phenotype by Budisteanu, M, Tutulan-Cunita, A, Papuc, S.M, Focsa, I, Vultur, S, Arghir, A, Grozavescu, R

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P138 – 3000: Neonatal brachial plexus palsy – Romanian single centre experience over 6 years by Craiu, D, Dica, A, Barca, D, Tarta-Arsene, O, Minciu, I, Iliescu, C, Burloiu, C, Butoianu, N, Budisteanu, M, Pomeran, C, Sandu, C, Gherghiceanu, R, Robanescu, L, Zamfirescu, D

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Real-World Experiences in Autistic Adult Diagnostic Services and Post-diagnostic Support and Alignment with Services Guidelines: Results from the ASDEU Study by Scattoni, Maria Luisa, Micai, Martina, Ciaramella, Antonio, Salvitti, Tommaso, Fulceri, Francesca, Fatta, Laura Maria, Poustka, Luise, Diehm, Robert, Iskrov, Georgi, Stefanov, Rumen, Guillon, Quentin, Rogé, Bernadette, Staines, Anthony, Sweeney, Mary Rose, Boilson, Andrew Martin, Leósdóttir, Thora, Saemundsen, Evald, Moilanen, Irma, Ebeling, Hanna, Yliherva, Anneli, Gissler, Mika, Parviainen, Tarja, Tani, Pekka, Kawa, Rafal, Vicente, Astrid, Rasga, Célia, Budişteanu, Magdalena, Dale, Ian, Povey, Carol, Flores, Noelia, Jenaro, Cristina, Monroy, Maria Luisa, Primo, Patricia García, Charman, Tony, Cramer, Susanne, Warberg, Christine Kloster, Canal-Bedia, Ricardo, Posada, Manuel, Schendel, Diana

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The impact of Moyamoya syndrome in a patient with neurofibromatosis type I by Focsa, I.O., Bohiltea, L.C., Burloiu, C., Budisteanu, M.

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Intervention Services for Autistic Adults: An ASDEU Study of Autistic Adults, Carers, and Professionals’ Experiences by Micai, Martina, Ciaramella, Antonio, Salvitti, Tommaso, Fulceri, Francesca, Fatta, Laura Maria, Poustka, Luise, Diehm, Robert, Iskrov, Georgi, Stefanov, Rumen, Guillon, Quentin, Rogé, Bernadette, Staines, Anthony, Sweeney, Mary Rose, Boilson, Andrew Martin, Leósdóttir, Thora, Saemundsen, Evald, Moilanen, Irma, Ebeling, Hanna, Yliherva, Anneli, Gissler, Mika, Parviainen, Tarja, Tani, Pekka, Kawa, Rafal, Vicente, Astrid, Rasga, Célia, Budişteanu, Magdalena, Dale, Ian, Povey, Carol, Flores, Noelia, Jenaro, Cristina, Monroy, Maria Luisa, Primo, Patricia García, Charman, Tony, Cramer, Susanne, Warberg, Christine Kloster, Canal-Bedia, Ricardo, Posada, Manuel, Scattoni, Maria Luisa, Schendel, Diana

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Phenotypic Variability of 17q12 Microdeletion Syndrome – Three Cases and Review of Literature by Țuțulan-Cuniță, A, Pavel, AG, Dimos, L, Nedelea, M, Ursuleanu, A, Neacșu, AT, Budișteanu, M, Stambouli, D

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Cerebral venous thrombosis in child the role of the early intervention by Budisteanu, M, Burloiu, C, Dumea, A.M, Magureanu, S

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P140Clinical caracterization of a new case with chromosome 3 terminal microdeletion, involving chl1 gene by Focsa, I O, Ioana, M, Streata, I, Sosoi, S Serban, Pirvu, A, Bohiltea, L C, Budisteanu, M

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P341 Behaviour phenotypes in children with chromosomal diseases by Budisteanu, M, Burloiu, C, Iliescu, C, Arghir, A, Chirieac, S.M, Lungeanu, A, Magureanu, S

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Autistic Adult Health and Professional Perceptions of It: Evidence From the ASDEU Project by Micai, Martina, Ciaramella, Antonio, Salvitti, Tommaso, Fulceri, Francesca, Fatta, Laura Maria, Poustka, Luise, Diehm, Robert, Iskrov, Georgi, Stefanov, Rumen, Guillon, Quentin, Rogé, Bernadette, Staines, Anthony, Sweeney, Mary Rose, Boilson, Andrew Martin, Leósdóttir, Thora, Saemundsen, Evald, Moilanen, Irma, Ebeling, Hanna, Yliherva, Anneli, Gissler, Mika, Parviainen, Tarja, Tani, Pekka, Kawa, Rafal, Vicente, Astrid, Rasga, Célia, Budişteanu, Magdalena, Dale, Ian, Povey, Carol, Flores, Noelia, Jenaro, Cristina, Monroy, Maria Luisa, Primo, Patricia García, Charman, Tony, Cramer, Susanne, Warberg, Christine Kloster, Canal-Bedia, Ricardo, Posada, Manuel, Scattoni, Maria Luisa, Schendel, Diana

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P.0343 Early detection, diagnosis and intervention services for children with autism spectrum disorder across europe according to the gross domestic product by Bejarano-Martín, Á., Canal-Bedia, R., Magán-Maganto, M., Fernández-Álvarez, C., Martín-Cilleros, M.V., Sánchez-Gómez, M.C., García-Primo, P., Rose-Sweeney, M., Boilson, A., Linertová, R., Roeyers, H., Van der Paelt, S., Schendel, D., Warberg, C., Cramer, S., Narzisi, A., Muratori, F., Scatonni, M.L., Moilanen, I., Yliherva, A., Saemundsen, E., Jónsdóttir, S.L., Efrim-Budisteanu, M., Arghir, A., Papuc, S. Mihaela, Vicente, A., Rasga, C., Rogé, B., Guillon, Q., Baduel, S., Kafka, J. Xenia, Kothgassner, O., Poustka, L., Kawa, R., Pisula, E., Sellers, T., de la Paz, M. Posada

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Autistic Adult Services Availability, Preferences, and User Experiences: Results From the Autism Spectrum Disorder in the European Union Survey by Micai, Martina, Fulceri, Francesca, Salvitti, Tommaso, Romano, Giovanna, Poustka, Luise, Diehm, Robert, Iskrov, Georgi, Stefanov, Rumen, Guillon, Quentin, Rogé, Bernadette, Staines, Anthony, Sweeney, Mary Rose, Boilson, Andrew Martin, Leósdóttir, Thora, Saemundsen, Evald, Moilanen, Irma, Ebeling, Hanna, Yliherva, Anneli, Gissler, Mika, Parviainen, Tarja, Tani, Pekka, Kawa, Rafal, Pisula, Eva, Vicente, Astrid, Rasga, Célia, Budişteanu, Magdalena, Dale, Ian, Povey, Carol, Flores, Noelia, Jenaro, Cristina, Monroy, Maria Luisa, Primo, Patricia García, Charman, Tony, Cramer, Susanne, Warberg, Christine Kloster, Canal-Bedia, Ricardo, Posada, Manuel, Schendel, Diana, Scattoni, Maria Luisa

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P140 Clinical caracterization of a new case with chromosome 3 terminal microdeletion, involving chl1 gene by Focsa, IO, Ioana, M, Streata, I, Sosoi, S Serban, Pirvu, A, Bohiltea, LC, Budisteanu, M

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