Search Results - "intellectually disabled"

LAYANAN TRANSISI DALAM RANGKA MENYIAPKAN KEMANDIRIAN FINANSIAL SISWA TUNAGRAHITA RINGAN DI SLBC PURNAMA ASIH BANDUNG by Asep Rudi Irawan, -

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KAJIAN KESESUAIAN PEMBELAJARAN MATEMATIKA DENGAN CAPAIAN PERKEMBANGAN KOGNITIF PADA ANAK TUNAGRAHITA KELAS SATU SDLB NPM by Hidayat, Lalu Rudy

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PENGARUH PENGGUNAAN MEDIA PUZZLE KATA BERGAMBAR TERHADAP PENINGKATAN KEMAMPUAN MEMBACA PERMULAAN PADA ANAK TUNAGRAHITA RINGAN DI SLB NEGERI BANJAR by Zakiyya Hafidza Tsany, -

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African Disability Rights Yearbook Volume 4 2016 by Charles Ngwena

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Gaboxadol in Fragile X Syndrome: A 12-Week Randomized, Double-Blind, Parallel-Group, Phase 2a Study by Dejan B. Budimirovic, Dejan B. Budimirovic, Kelli C. Dominick, Kelli C. Dominick, Lidia V. Gabis, Lidia V. Gabis, Maxwell Adams, Mathews Adera, Linda Huang, Pamela Ventola, Nicole R. Tartaglia, Elizabeth Berry-Kravis

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Issues of Inclusion and Special Education in the Creative Heritage of Sofia Rusova by Oksana Dzhus

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Novel ANKRD11 gene mutation in an individual with a mild phenotype of KBG syndrome associated to a GEFS+ phenotypic spectrum: a case report by Rita Maria Alves, Paolo Uva, Marielza F. Veiga, Manuela Oppo, Fabiana C. R. Zschaber, Giampiero Porcu, Henrique P. Porto, Ivana Persico, Stefano Onano, Gianmauro Cuccuru, Rossano Atzeni, Lauro C. N. Vieira, Marcos V. A. Pires, Francesco Cucca, Maria Betânia P. Toralles, Andrea Angius, Laura Crisponi

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Mental health impact of autism on families of children with intellectual and developmental disabilities of genetic origin by Jeanne Wolstencroft, Ramya Srinivasan, Jeremy Hall, Marianne B. M. van denBree, Michael J. Owen, IMAGINE Consortium, F. Lucy Raymond, David Skuse

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Developing antisense oligonucleotides for a TECPR2 mutation-induced, ultra-rare neurological disorder using patient-derived cellular models by Luis A. Williams, David J. Gerber, Amy Elder, Wei Chou Tseng, Valeriya Baru, Nathaniel Delaney-Busch, Christina Ambrosi, Gauri Mahimkar, Vaibhav Joshi, Himali Shah, Karthiayani Harikrishnan, Hansini Upadhyay, Sakthi H. Rajendran, Aishwarya Dhandapani, Joshua Meier, Steven J. Ryan, Caitlin Lewarch, Lauren Black, Julie Douville, Stefania Cinquino, Helen Legakis, Karsten Nalbach, Christian Behrends, Ai Sato, Lorenzo Galluzzi, Timothy W. Yu, Duncan Brown, Sudhir Agrawal, David Margulies, Alan Kopin, Graham T. Dempsey

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Clinical characteristics and genetics of ten Chinese children with PRRT2-associated neurological diseases by Meiyan Liu, Xiaoang Sun, Longlong Lin, Xiaona Luo, Simei Wang, Chunmei Wang, Yuanfeng Zhang, Quanmei Xu, Wuhen Xu, Shengnan Wu, Xiaoping Lan, Yucai Chen, Yucai Chen

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Clinical Forms and GRIN2A Genotype of Severe End of Epileptic-Aphasia Spectrum Disorder by Xiao Li, Xiao Li, Xiao Li, Xiao Li, Xiao Li, Ling-Ling Xie, Ling-Ling Xie, Ling-Ling Xie, Ling-Ling Xie, Ling-Ling Xie, Wei Han, Wei Han, Wei Han, Wei Han, Wei Han, Si-Qi Hong, Si-Qi Hong, Si-Qi Hong, Si-Qi Hong, Si-Qi Hong, Jian-Nan Ma, Jian-Nan Ma, Jian-Nan Ma, Jian-Nan Ma, Jian-Nan Ma, Juan Wang, Juan Wang, Juan Wang, Juan Wang, Juan Wang, Li Jiang, Li Jiang, Li Jiang, Li Jiang, Li Jiang

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Drug-induced gingival hyperplasia: a retrospective study using spontaneous reporting system databases by Haruna Hatahira, Junko Abe, Yuuki Hane, Toshinobu Matsui, Sayaka Sasaoka, Yumi Motooka, Shiori Hasegawa, Akiho Fukuda, Misa Naganuma, Tomofumi Ohmori, Yasutomi Kinosada, Mitsuhiro Nakamura

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اثربخشی آموزش قصه‌های مبتنی بر دیالوگ بر مهارت‌های زبانی کودکان دختر کم‌توان هوشی آموزش‌پذیر مقطع دبستان... by Afrooz Makarem-Nasab, Ahmad Yarmohammadian, Amir Ghamarani

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Correlating maternal iodine status with neonatal thyroid function in two hospital populations in Ghana: a multicenter cross-sectional pilot study by Selorm A. Dei-Tutu, Adoma Manful, Douglas C. Heimburger, Hawa Malechi, Daniel J. Moore, Samuel A. Oppong, William E. Russell, Muktar H. Aliyu

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Long contiguous stretches of homozygosity detected by chromosomal microarrays (CMA) in patients with neurodevelopmental disorders in the South of Brazil by Tiago Fernando Chaves, Luan Freitas Oliveira, Maristela Ocampos, Ingrid Tremel Barbato, Gisele Rozone de Luca, Jorge Humbeto Barbato Filho, Louise Lapagesse de Camargo Pinto, Pricila Bernardi, Angelica Francesca Maris

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Chromosomal microarrays testing in children with developmental disabilities and congenital anomalies by Guillermo Lay-Son, Karena Espinoza, Cecilia Vial, Juan C. Rivera, María L. Guzmán, Gabriela M. Repetto

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PENGEMBANGAN PROGRAM PEMBELAJARAN UNTUK MENINGKATKAN KEMAMPUAN MEMBACA PERMULAAN PADA ANAK TUNAGRAHITA RINGAN DI SLB NURVITA by Putri, Wini Nurvita

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A retrospective review of the common childhood illnesses and the indications for antibiotic prescription at community hospital in Malawi by Adriano Focus Lubanga, Adriano Focus Lubanga, Chana Khuluza, Chana Khuluza, Jamillah Muhyuddin, Jamillah Muhyuddin, Reuben Simfukwe, Reuben Simfukwe, Frank Kaphesi, Yeo Hwan Yeum, Joshua J. Yoon, Changwoo Kim, Seunghyun Kim, Si Yeon Kim, Ji An Lee, Jooheon Park, Jooheon Park, David Kim, Akim Nelson Bwanali, Akim Nelson Bwanali, Lee Woohyung, Thomas Nyirenda, Thomas Nyirenda

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Clinical findings and genetic analysis of patients with copy number variants involving 17p13.3 using a single nucleotide polymorphism array: a single-center experience by Bin Liang, Donghong Yu, Wantong Zhao, Yan Wang, Xiaoqing Wu, Lingji Chen, Na Lin, Hailong Huang, Liangpu Xu

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Researching outcomes from forensic services for people with intellectual or developmental disabilities: a systematic review, evidence synthesis and expert and patient/carer consult... by Catrin Morrissey, Nicole Geach, Regi Alexander, Verity Chester, John Devapriam, Conor Duggan, Peter E Langdon, Bill Lindsay, Jane McCarthy, Dawn-Marie Walker

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