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Journal of Autism and Developmental Disorders|May 9, 2021
Intervention Services for Autistic Adults: An ASDEU Study of Autistic Adults, Carers, and Professionals' ExperiencesMartina Micai, Antonio Ciaramella, Tommaso Salvitti, et al.
Journal of Autism and Developmental Disorders|November 30, 2019
Correction to: Early Detection, Diagnosis and Intervention Services for Young Children with Autism Spectrum Disorder in the European Union (ASDEU): Family and Professional PerspectivesÁlvaro Bejarano-Martín, Ricardo Canal-Bedia, María Magán-Maganto, et al.
Journal of Autism and Developmental Disorders|October 14, 2019
Early Detection, Diagnosis and Intervention Services for Young Children with Autism Spectrum Disorder in the European Union (ASDEU): Family and Professional PerspectivesÁlvaro Bejarano-Martín, Ricardo Canal-Bedia, María Magán-Maganto, et al.
Autism : the International Journal of Research and Practice|March 9, 2022
Determinants of satisfaction with the detection process of autism in Europe: Results from the ASDEU studyQuentin Guillon, Sophie Baduel, Álvaro Bejarano-Martín, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 22, 2023
A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencingAnne-Sophie Denommé-Pichon, Leslie Matalonga, Elke de Boer, et al.
Environmental Research|February 11, 2015
Fish consumption patterns and hair mercury levels in children and their mothers in 17 EU countriesArgelia Castaño, Francisco Cutanda, Marta Esteban, et al.
Human Mutation|February 18, 2022
The RD-Connect Genome-Phenome Analysis Platform: Accelerating diagnosis, research, and gene discovery for rare diseasesSteven Laurie, Davide Piscia, Leslie Matalonga, et al.
Advances in Experimental Medicine and Biology|December 8, 2017
Improved Diagnosis and Care for Rare Diseases through Implementation of Precision Public Health FrameworkGareth Baynam, Faye Bowman, Karla Lister, et al.
Human Mutation|January 22, 2015
The TREAT-NMD DMD Global Database: analysis of more than 7,000 Duchenne muscular dystrophy mutationsCatherine L Bladen, David Salgado, Soledad Monges, et al.
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