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

Volltext

Abundant pleiotropy across neuroimaging modalities identified through a multivariate genome-wide association study von 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.

Volltext

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

Volltext

Multidisciplinary approach in children with autism spectrum disorder von 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.

Volltext

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

Volltext

Behavior problems associated with brain heterotopia von 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.

Volltext

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

Volltext

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

Volltext

P138 – 3000: Neonatal brachial plexus palsy – Romanian single centre experience over 6 years von 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

Volltext

Real-World Experiences in Autistic Adult Diagnostic Services and Post-diagnostic Support and Alignment with Services Guidelines: Results from the ASDEU Study von 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

Volltext

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

Volltext

Intervention Services for Autistic Adults: An ASDEU Study of Autistic Adults, Carers, and Professionals’ Experiences von 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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

P.0343 Early detection, diagnosis and intervention services for children with autism spectrum disorder across europe according to the gross domestic product von 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

Volltext

Autistic Adult Services Availability, Preferences, and User Experiences: Results From the Autism Spectrum Disorder in the European Union Survey von 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

Volltext

Chromosome Y Isodicentrics in two Cases with Ambiguous genitalia and Features of Turner Syndrome von Lungeanu, A, Arghir, A, Arps, S, Cardos, G, Dumitriu, N, Budisteanu, M, Chirieac, S, Rodewald, A

Volltext

Early-onset multiple sclerosis: clinical and evolutive features von Burloiu, C, Iliescu, C, Barca, D, Dumea, A, Magureanu, S, Gherghiceanu, R, Minciu, I, Godeanu, S, Craiu, D, Budisteanu, M, Burloiu, A

Volltext