Search Results - "intellectually disabled"

BEHAVIORAL CHARACTERISTICS OF CHILDREN WITH SICKLE CELL DISEASE by Fellipe Bondança Pereira, Glaura César Pedroso, Rosa Miranda Resegue, Marcos Vinicius Vieira Ribeiro, Mary Hokazono, Josefina Aparecida Pellegrini Braga

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Konsep Diri dan Resiliensi Orangtua yang Memiliki Anak Tunagrahita by Eugennia Sakanti Putri, Ketut Suryani, Novita Elisabeth Daeli

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A Review of Disparities and Unmet Newborn Screening Needs over 33 Years in a Cohort of Mexican Patients with Inborn Errors of Intermediary Metabolism by Isabel Ibarra-González, Cynthia Fernández-Lainez, Marcela Vela-Amieva, Sara Guillén-López, Leticia Belmont-Martínez, Lizbeth López-Mejía, Rosa Itzel Carrillo-Nieto, Nidia Alejandra Guillén-Zaragoza

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Intellectual and developmental disability nursing: current challenges in the USA by Auberry K

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PPAR-gamma agonist pioglitazone recovers mitochondrial quality control in fibroblasts from PITRM1-deficient patients by Alessia Di Donfrancesco, Christian Berlingieri, Marta Giacomello, Marta Giacomello, Chiara Frascarelli, Ana Paula Magalhaes Rebelo, Laurence A. Bindoff, Segel Reeval, Paul Renbaum, Filippo M. Santorelli, Giulia Massaro, Carlo Viscomi, Massimo Zeviani, Daniele Ghezzi, Daniele Ghezzi, Emanuela Bottani, Dario Brunetti, Dario Brunetti

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Oral health knowledge, attitudes, and practices of people living with mental illness: a mixed-methods systematic review by Alisha Maree Johnson, Amanda Kenny, Lucie Ramjan, Toby Raeburn, Ajesh George

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Burdens of Rubella and Cytomegalovirus infections among pregnant women in Africa: A systematic review and meta-analysis by Addis Eyeberu, Adera Debella, Bikila Balis, Magarsa Lami, Tigist Tefera, Tamirat Getachew

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Reduced anogenital distance, hematuria and left renal hypoplasia in a patient with 13q33.1-34 deletion: case report and literature review by Xue He, Huijun Shen, Haidong Fu, Chunyue Feng, Zhixia Liu, Yanyan Jin, Jianhua Mao

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Clinical and molecular genetic characterization of familial MECP2 duplication syndrome in a Chinese family by Xiaoyan Li, Hua Xie, Qian Chen, Xiongying Yu, Zhaoshi Yi, Erzhen Li, Ting Zhang, Jian Wang, Jianmin Zhong, Xiaoli Chen

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Genetic outcomes in children with developmental language disorder: a systematic review by Vivian van Wijngaarden, Hester de Wilde, Dieuwke Mink van der Molen, Jildo Petter, Inge Stegeman, Inge Stegeman, Ellen Gerrits, Ellen Gerrits, Adriana L. Smit, Adriana L. Smit, Marie-José van den Boogaard

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Case Report: Mucolipidosis II and III Alpha/Beta Caused by Pathogenic Variants in the GNPTAB Gene (Mucolipidosis) by Shao-Jia Mao, Yu-Mei Zu, Yang-Li Dai, Chao-Chun Zou

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Feeding and Eating Disorder and Risk of Subsequent Neurodevelopmental Disorders: A Population-Based Cohort Study by Hongyun Shan, Hongyun Shan, Hongyun Shan, Fei Li, Jun Zhang, Hui Wang, Jiong Li, Jiong Li, Jiong Li

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RESEARCH IMPLEMENTATION OF CORRECTIONAL COMPONENT FOR INDIVIDUAL LEARNING OF CHILDREN WITH COGNITIVE IMPAIRMENT by Dutkovska, R.V

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Medical classification in sport of disabled people by Beniamin Szmelcer, Agata Trzebiatowska, Michał Wilczyński, Paulina Miętkowska, Małgorzata Gajos, Natalia Skierkowska, Monika Prylińska, Jakub Husejko, Oktawia Wysocka, Weronika Topka, Magdalena Łabędź, Kornelia Kędziora-Kornatowska

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Short Bones, Renal Stones, and Diagnostic Moans: Hypercalcemia in a Girl Found to Have Coffin-Lowry Syndrome by Christina G. Tise MD, PhD, Dena R. Matalon MD, Melanie A. Manning MD, Heather M. Byers MD, Monica Grover MBBS

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Very-Low-Dose Levodopa Therapy for Pediatric Neurological Disorders: A Preliminary Questionnaire in Japan by Kyoko Hoshino, Kyoko Hoshino, Kyoko Hoshino, Masaharu Hayashi, Masaharu Hayashi, Masaharu Hayashi, Asayo Ishizaki, Asayo Ishizaki, Kazue Kimura, Kazue Kimura, Masaya Kubota, Masaya Kubota, Atsuo Nezu, Atsuo Nezu, Akihiro Yasuhara, Akihiro Yasuhara

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The role of behavioral phenotyping in establishing a diagnosis of pseudo-angelman syndrome by Veronica Arora, Aashita Takkar, Sameer Bhatia, Meena Lall, Praveen Kumar

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Fragile X mental retardation protein regulates trans-synaptic signaling in Drosophila by Samuel H. Friedman, Neil Dani, Emma Rushton, Kendal Broadie

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Spinocerebellar ataxia type 13 mutation that is associated with disease onset in infancy disrupts axonal pathfinding during neuronal development by Fadi A. Issa, Allan F. Mock, Alvaro Sagasti, Diane M. Papazian

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Bardet-Biedl Syndrome: a case report of delayed diagnosis with variable presentation and role of genetic testing in definitive diagnosis by Gargi Ramesh Rekhawar, M. P. Bhavana, Vishal Dnyaneshwar Sawant, Sushma Save, Alpana Kondekar

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