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2621por Morin, Sébastien, Moak, Hannah Barron, Bubb-Humfryes, Oliver, von Drehle, Christian, Lazarus, Jeffrey V, Burrone, EstebanEnlace del recurso
Publicado 2022
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2622“…OBJECTIVE: To analyze genetic mutations in a Chinese pedigree affected with Alpha-thalassemia X-linked intellectual disability syndrome, providing a precise diagnosis and genetic counseling. …”
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2623“…METHODS: A multiple-case study was conducted in a care organization for people with intellectual disabilities and/or acquired brain injury, by observing MCD sessions as ‘cases’, followed by interviews with health care professionals concerning the follow-up to these cases, and a focus group with involved MCD facilitators. …”
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2624por Almalki, Nabil Sharaf“…Augmentative and alternative communication systems have been successfully used to help pupils with intellectual and developmental disabilities for functional communication skills. …”
Publicado 2022
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2625por Brant, Boris, Stern, Tchelet, Shekhidem, Huda Adwan, Mizrahi, Liron, Rosh, Idan, Stern, Yam, Ofer, Polina, Asleh, Ayat, Umanah, George K. Essien, Jada, Reem, Levy, Nina S., Levy, Andrew P., Stern, Shani“…Mutations in the IQSEC2 gene are associated with drug-resistant, multifocal infantile and childhood epilepsy; autism; and severe intellectual disability (ID). We used induced pluripotent stem cell (iPSC) technology to obtain hippocampal neurons to investigate the neuropathology of IQSEC2-mediated disease. …”
Publicado 2021
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2626“…While perceived social support has emerged as an important protective factor, this effect has not been replicated in people with intellectual disabilities (ID). One reason for this might be that the relevance of socio-interpersonal factors differs in people with ID: Social support may be associated with more stress due to a generally high dependency on sometimes unwanted support. …”
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2627por Walker, Adrian Raymond, Trollor, Julian Norman, Florio, Tony, Srasuebkul, Preeyaporn“…Adults with intellectual disability have high health care needs. …”
Publicado 2022
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2628por Saeed, Gul, Brown, Hilary K., Lunsky, Yona, Welsh, Kate, Proulx, Laurie, Havercamp, Susan, Tarasoff, Lesley A.“…What constitutes “effective communication” in perinatal care may vary according to the population seeking care, such as women with intellectual and developmental disabilities (IDD) and sensory disabilities. …”
Publicado 2022
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2629por Ng-Cordell, Elise, Kolesnik-Taylor, Anna, O’Brien, Sinéad, Astle, Duncan, Scerif, Gaia, Baker, Kate“…DDX3X variants are a common cause of intellectual disability (ID) in females, and have been associated with autism spectrum disorder and emotional-behavioural difficulties. …”
Publicado 2022
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2630“…This result demonstrates that artificial intelligence is positively correlated with the external input information. Intellectual property management is a crucial guarantee of open technology innovation in the ICT industry. …”
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2631por Waqas, Ahmed, Nayab, Anam, Shaheen, Shabnam, Abbas, Safdar, Latif, Muhammad, Rafeeq, Misbahuddin M., Al-Dhuayan, Ibtesam S., Alqosaibi, Amany I., Alnamshan, Mashael M., Sain, Ziaullah M., Habib, Alaa Hamed, Alam, Qamre, Umair, Muhammad, Saqib, Muhammad Arif Nadeem“…Intellectual disability (ID) has become very common and is an extremely heterogeneous disorder, where the patients face many challenges with deficits in intellectual functioning and adaptive behaviors. …”
Publicado 2022
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2632por Zhang, Ying, Nie, Yanyan, Mu, Yu, Zheng, Jie, Xu, Xiaowei, Zhang, Fang, Shu, Jianbo, Liu, YangEnlace del recurso
Publicado 2022
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2633por Borilli, Marcela Cesaretti, Germano, Carla Maria Ramos, de Avó, Lucimar Retto da Silva, Pilotto, Rui Fernando, Melo, Débora Gusmão“…BACKGROUND: Intellectual disability (ID) and autism spectrum disorder (ASD) are often concomitant childhood developmental disorders. …”
Publicado 2022
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2634por Layne, Charles S., Malaya, Christopher A., Young, David R., Suter, Berhard, Holder, Jimmy L.“…SYNGAP1-related Intellectual Disability (SYNGAP1-ID) is a rare neurodevelopmental condition characterized by profound intellectual disability, gross motor delays, and behavioral issues. …”
Publicado 2022
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2635por Perehudoff, Katrina, 't Hoen, Ellen, Mara, Kaitlin, Balasubramaniam, Thirukumaran, Abbott, Frederick, Baker, Brook, Boulet, Pascale, Kamal-Yanni, Mohga, Martin, Manuel, Munoz Tellez, Viviana, Natsis, Yannis, Ortún-Rubio, Vicente, Rathod, Sandeep, Torrent, Maties, Vawda, Yousuf, Villarroel, Luis, Love, JamesEnlace del recurso
Publicado 2022
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2636“…BACKGROUND: A rights‐based agenda, informed by the UNCRPD, that advocates person‐centredness, inclusion, empowerment and self‐determination is shaping service provision to people with intellectual disability (ID). Listening to their perspectives is fundamental to meeting these goals. …”
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2637por Tan, Bhing-Leet, Guan, Frank Yunqing, Leung, Ivy Mun Wah, Kee, Sharon Yi-May, Devilly, Oran Zane, Medalia, Alice“…This pilot study aimed to explore the acceptability and effectiveness of the REAP program when carried out with adults with intellectual and developmental disabilities attending work therapy. …”
Publicado 2022
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2638por Scheper, Mirte, Romagnolo, Alessia, Besharat, Zein Mersini, Iyer, Anand M., Moavero, Romina, Hertzberg, Christoph, Weschke, Bernhard, Riney, Kate, Feucht, Martha, Scholl, Theresa, Petrak, Borivoj, Maulisova, Alice, Nabbout, Rima, Jansen, Anna C., Jansen, Floor E., Lagae, Lieven, Urbanska, Malgorzata, Ferretti, Elisabetta, Tempes, Aleksandra, Blazejczyk, Magdalena, Jaworski, Jacek, Kwiatkowski, David J., Jozwiak, Sergiusz, Kotulska, Katarzyna, Sadowski, Krzysztof, Borkowska, Julita, Curatolo, Paolo, Mills, James D., Aronica, Eleonora“…Tuberous sclerosis complex (TSC) is a rare multi-system genetic disorder characterized by a high incidence of epilepsy and neuropsychiatric manifestations known as tuberous-sclerosis-associated neuropsychiatric disorders (TANDs), including autism spectrum disorder (ASD) and intellectual disability (ID). MicroRNAs (miRNAs) are small regulatory non-coding RNAs that regulate the expression of more than 60% of all protein-coding genes in humans and have been reported to be dysregulated in several diseases, including TSC. …”
Publicado 2022
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2640por Nagai, Masayoshi, Iemura, Kenji, Kikkawa, Takako, Naher, Sharmin, Hattori, Satoko, Hagihara, Hideo, Nagata, Koh-ichi, Anzawa, Hayato, Kugisaki, Risa, Wanibuchi, Hideki, Abe, Takaya, Inoue, Kenichi, Kinoshita, Kengo, Miyakawa, Tsuyoshi, Osumi, Noriko, Tanaka, Kozo“…CHAMP1 is a gene associated with intellectual disability, which was originally identified as being involved in the maintenance of kinetochore–microtubule attachment. …”
Publicado 2022
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