Search Results - "intellectually disabled"

Exploring the Correlation between Peer Attachment and Emotional Regulation in Indonesian Special Needs Education by Made Loka Santi Ari, Christiana Hari Soetjiningsih

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An unusual presentation of fucosidosis in a Chinese boy: a case report and literature review (childhood fucosidosis) by Shao-Jia Mao, Jia Zhao, Zheng Shen, Chao-Chun Zou

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Whole Exome Sequencing Identifies Three Novel Mutations in the ASPM Gene From Saudi Families Leading to Primary Microcephaly by Muhammad Imran Naseer, Muhammad Imran Naseer, Angham Abdulrahman Abdulkareem, Angham Abdulrahman Abdulkareem, Osama Yousef Muthaffar, Sameera Sogaty, Hiba Alkhatabi, Hiba Alkhatabi, Sarah Almaghrabi, Sarah Almaghrabi, Adeel G. Chaudhary, Adeel G. Chaudhary, Adeel G. Chaudhary

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Impacto da deficiência intelectual moderada na dinâmica e na qualidade de vida familiar: um estudo clínico-qualitativo by Rodrigo Victor Viana Tomaz, Vanessa de Arruda Santos, Lucimar Retto da Silva de Avó, Carla Maria Ramos Germano, Débora Gusmão Melo

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Un progetto per l'apprendimento della matematica nella scuola primaria per bambini con sindrome di Down: Fenix Didò by Cecilia Maria Marchisio, Natascia Curto

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Gillespie syndrome in a South Asian child: a case report with confirmation of a heterozygous mutation of the ITPR1 gene and review of the clinical and molecular features by Daham De Silva, Kathleen A. Williamson, Kavinda Chandimal Dayasiri, Nayani Suraweera, Vinushiya Quinters, Hiranya Abeysekara, Jithangi Wanigasinghe, Deepthi De Silva, Harendra De Silva

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Dental Treatment Under General Anesthesia in a Day Care Surgery Setting by Vlaho Brailo, Bernard Janković, Marin Lozić, Dragana Gabrić, Tihomir Kuna, Vasilije Stambolija, Željko Verzak

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Congenital Hypothyroidism: Increased Incidence in Yazd Province, Iran by M. Noori-Shadkam, M.H. Mosadegh, M. Mirzaei, MR. Movahedi Nia, M. Jafarizadeh

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Conscious sedation, general anaesthesia for patients with special needs by David Fu, Claudia Lopez-Silva, Laurence J Walsh, Archana Pradhan

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Recurrent myocardial injury in a de novo SON mutation ZTTK syndrome patient: a case report by Jia Na, Lang Cui, Zhen Zhen, Xi Chen, Qirui Li, Lu Gao, Yue Yuan

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A Randomised Crossover Trial of Behaviour Guidance Techniques on Children with Special Health Care Needs during Dental Treatment: The Physiological Variations by Norsaima Ismail, Khairil Anuar Md Isa, Ilham Wan Mokhtar

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The L1 cell adhesion molecule constrains dendritic spine density in pyramidal neurons of the mouse cerebral cortex by Kelsey E. Murphy, Kelsey E. Murphy, Sarah D. Wade, Sarah D. Wade, Justin E. Sperringer, Justin E. Sperringer, Vishwa Mohan, Vishwa Mohan, Bryce W. Duncan, Bryce W. Duncan, Erin Y. Zhang, Erin Y. Zhang, Yubin Pak, Yubin Pak, David Lutz, Melitta Schachner, Patricia F. Maness, Patricia F. Maness

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Rubinstein-Taybi syndrome in a Saudi boy with distinct features and variants in both the CREBBP and EP300 genes: a case report by Mohammad M. Al-Qattan, Abdulaziz Jarman, Atif Rafique, Zuhair N. Al-Hassnan, Heba M. Al-Qattan

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The association between non-standard employment, job insecurity and health among British adults with and without intellectual impairments: Cohort study by Eric Emerson, Chris Hatton, Janet Robertson, Susannah Baines

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Calidad de vida en niños y adolescentes con parálisis cerebral by Egmar Longo Araújo de Melo, Marta Badia Corbella, María Begoña Orgaz Baz, Miguel Ángel Verdugo Alonso, Benito Arias Martínez, María Gómez-Vela, Francisca González-Gil, Ana M. Ullán

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LETM1 haploinsufficiency causes mitochondrial defects in cells from humans with Wolf-Hirschhorn syndrome: implications for dissecting the underlying pathomechanisms in this conditi... by Lesley Hart, Anita Rauch, Antony M. Carr, Joris R. Vermeesch, Mark O'Driscoll

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Aleitamento materno em crianças com microcefalia por síndrome congênita do vírus Zika by Karole Brito Alves Costa, Normeide Pedreira dos Santos França

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Understanding copy number variations through their genes: a molecular view on 16p11.2 deletion and duplication syndromes by Roberta Leone, Cecilia Zuglian, Riccardo Brambilla, Riccardo Brambilla, Ilaria Morella

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Children with FASD-Evolving Patterns of Developmental Problems and Intervention Costs in Ages 0 through 16 in Finland by Laura Mirjami Jolma, Mikko Koivu-Jolma, Anne Sarajuuri, Paulus Torkki, Ilona Autti-Rämö, Heli Sätilä

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Updates on Clinical and Genetic Heterogeneity of ASPM in 12 Autosomal Recessive Primary Microcephaly Families in Pakistani Population by Niaz Muhammad Khan, Basharat Hussain, Basharat Hussain, Chenqing Zheng, Ayaz Khan, Muhammad Shareef Masoud, Qingquan Gu, Linhui Qiu, Naveed Altaf Malik, Muhammad Qasim, Muhammad Tariq, Junlei Chang

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