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All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year Sort by creator [A → Z]' creator [Z → A]' publishing year ↑ (asc)' publishing year ↓ (desc)' title [A → Z]' title [Z → A]' Simple Search Page: 1 2 Hits 1 – 20 of 36 1 Examining the barriers to accessing and utilizing healthcare services for minority-language speakers with neurodevelopmental disorders: a scoping review ... Beauchamp, Myriam. - : Open Science Framework, 2022 BASE Show details 2 Artificial Intelligence Enabled Personalised Assistive Tools to Enhance Education of Children with Neurodevelopmental Disorders—A Review Prabal Datta Barua; Jahmunah Vicnesh; Raj Gururajan; Shu Lih Oh; Elizabeth Palmer; Muhammad Mokhzaini Azizan; Nahrizul Adib Kadri; U. Rajendra Acharya In: International Journal of Environmental Research and Public Health; Volume 19; Issue 3; Pages: 1192 (2022) BASE Show details 3 Differences and Commonalities in Children with Childhood Apraxia of Speech and Comorbid Neurodevelopmental Disorders: A Multidimensional Perspective Anna Maria Chilosi; Irina Podda; Ivana Ricca; Alessandro Comparini; Beatrice Franchi; Simona Fiori; Rosa Pasquariello; Claudia Casalini; Paola Cipriani; Filippo Maria Santorelli In: Journal of Personalized Medicine; Volume 12; Issue 2; Pages: 313 (2022) BASE Show details 4 Medical teachers’ opinions about students with neurodevelopmental disorders and their management Magnin, Eloi; Ryff, Ilham; Moulin, Thierry In: ISSN: 1472-6920 ; BMC Medical Education ; https://hal-univ-fcomte.archives-ouvertes.fr/hal-03630125 ; BMC Medical Education, BioMed Central, 2021, 21 (1), pp.16. ⟨10.1186/s12909-020-02413-w⟩ (2021) BASE Show details 5 Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction den Hoed, Joery; de Boer, Elke; Voisin, Norine... In: ISSN: 0002-9297 ; EISSN: 1537-6605 ; American Journal of Human Genetics ; https://hal-univ-rennes1.archives-ouvertes.fr/hal-03268683 ; American Journal of Human Genetics, Elsevier (Cell Press), 2021, 108 (2), pp.346-356. ⟨10.1016/j.ajhg.2021.01.007⟩ (2021) BASE Show details 6 Maternal Occupation Exposures to Nanoscale Particles and Child Development ; Exposition professionnelle maternelle aux particules nanométriques et développement de l’enfant Manangama Duki, Guyguy. - : HAL CCSD, 2021 In: https://tel.archives-ouvertes.fr/tel-03368170 ; Médecine humaine et pathologie. Université de Bordeaux, 2021. Français. ⟨NNT : 2021BORD0182⟩ (2021) BASE Show details 7 Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders Devanna, P; Chen, X S; Ho, J. - 2021 BASE Show details 8 Capacity of the CCC-2 to Discriminate ASD from Other Neurodevelopmental Disorders Durán-Bouza, Montserrat; Pérez-Pereira, Miguel; De la Torre Carril, Alba. - 2021 BASE Show details 9 Parenting Stress and Language Development in Children: Associations in Angelman Syndrome and Down Syndrome Bland, Annalise; Husain, Zainab; Martin-O'Dell, Breanna... In: The Journal of Purdue Undergraduate Research (2021) BASE Show details 10 A Critical Review of Spatial Abilities in Down and Williams Syndromes: Not All Space Is Created Equal. Banta Lavenex, P.; Lavenex, P. In: Frontiers in psychiatry, vol. 12, pp. 669320 (2021) BASE Show details 11 Performance of the German version of the PARCA-R questionnaire as a developmental screening tool in two-year-old very preterm infants Picotti, Eleonora; Bechtel, Nina; Latal, Beatrice... In: ISSN: 1932-6203 ; PLOS ONE, Vol. 15, No 9 (2020) P. e0236289 (2020) BASE Show details 12 Metformin treatment in young children with fragile X syndrome. Biag, Hazel Maridith B; Potter, Laura A; Wilkins, Victoria... In: Molecular genetics & genomic medicine, vol 7, iss 11 (2019) BASE Show details 13 Pathogenic variants in USP7 cause a neurodevelopmental disorder with speech delays, altered behavior, and neurologic anomalies. Fountain, Michael D; Oleson, David S; Rech, Megan E... In: Genetics in medicine : official journal of the American College of Medical Genetics, vol 21, iss 8 (2019) BASE Show details 14 STXBP1-associated neurodevelopmental disorder: a comparative study of behavioural characteristics. ... O'Brien, Sinéad; Ng-Cordell, Elise; DDD Study. - : Apollo - University of Cambridge Repository, 2019 BASE Show details 15 Neurodevelopmental outcomes of children born to opioid-dependent mothers: a systematic review and meta-analysis Lee, Samantha J.; Bora, Samudragupta; Austin, Nicola C.. - : Elsevier, 2019 BASE Show details 16 Phonological processing in students with developmental dyslexia, ADHD and intellectual disability Ana Beatriz Leite dos Anjos; Alexandre Lucas de Araújo Barbosa; Cíntia Alves Salgado Azoni In: Revista CEFAC, Vol 21, Iss 5 (2019) (2019) BASE Show details 17 Anomalous morphology in left hemisphere motor and premotor cortex of children who stutter Nieto-Castañón, Alfonso; Chang, Soo-Eun; Guenther, Frank H.. - : Oxford University Press, 2018 BASE Show details 18 Read and write with all your senses: a multisensory method for learning to read and write in neurodevelopmental disorders Santos, Catarina; Martins, Catarina; Silva, Ana Isabel. - : Georgian Association of Child Neurologists and Neurosurgeons & Georgian Academy of Childhood Disability, 2018 BASE Show details 19 Pragmatic language and theory of mind in children with symptoms of ADHD: relationships with executive functions Green, Benita Christine. - 2018 BASE Show details 20 Neither action nor phonological video games make dyslexic children read better Łuniewska, Magdalena; Chyl, Katarzyna; Dębska, Agnieszka. - : Nature Publishing Group, 2018 BASE Show details Page: 1 2

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