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Showing results (41-50 of 54) with videos related to

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Autism Research : Official Journal of the International Society for Autism Research|August 19, 2018
Na<sup>+</sup> , K<sup>+</sup> -ATPase activity in children with autism spectrum disorder: Searching for the reason(s) of its decrease in blood cellsAlessandra Bolotta, Paola Visconti, Giorgio Fedrizzi, et al.
Oxidative Medicine and Cellular Longevity|January 5, 2019
Oxidative Stress in Autistic Children Alters Erythrocyte Shape in the Absence of Quantitative Protein Alterations and of Loss of Membrane Phospholipid AsymmetryAlessandra Bolotta, Michela Battistelli, Elisabetta Falcieri, et al.
Brain Sciences|October 21, 2020
Brain Magnetic Resonance Findings in 117 Children with Autism Spectrum Disorder under 5 Years OldMagali Jane Rochat, Giacomo Distefano, Monica Maffei, et al.
Molecular Autism|February 27, 2018
Advanced glycation endproducts, dityrosine and arginine transporter dysfunction in autism - a source of biomarkers for clinical diagnosisAttia Anwar, Provvidenza Maria Abruzzo, Sabah Pasha, et al.
Frontiers in Psychiatry|March 30, 2022
Contribution of <i>CACNA1H</i> Variants in Autism Spectrum Disorder SusceptibilityMarta Viggiano, Tiziano D'Andrea, Cinzia Cameli, et al.
Scientific Reports|August 31, 2017
High predictive values of RBC membrane-based diagnostics by biophotonics in an integrated approach for Autism Spectrum DisordersGiorgia Giacometti, Carla Ferreri, Anna Sansone, et al.
Neurology|March 6, 2016
The syndrome of polymicrogyria, thalamic hypoplasia, and epilepsy with CSWSEmanuele Bartolini, Melania Falchi, Francesco Zellini, et al.
Research Square|November 14, 2023
Whole genome analysis of rare deleterious variants adds further evidence to BRSK2 and other risk genes in Autism Spectrum DisorderElena Bacchelli, Marta Viggiano, Fabiola Ceroni, et al.
NPJ Genomic Medicine|March 23, 2024
Genomic analysis of 116 autism families strengthens known risk genes and highlights promising candidatesMarta Viggiano, Fabiola Ceroni, Paola Visconti, et al.
Journal of Cellular and Molecular Medicine|January 21, 2021
An increased burden of rare exonic variants in NRXN1 microdeletion carriers is likely to enhance the penetrance for autism spectrum disorderCinzia Cameli, Marta Viggiano, Magali J Rochat, et al.
Pageof 6

Showing results (41-50 of 54) with videos related to

Sort By:
Pageof 6
Autism Research : Official Journal of the International Society for Autism Research|August 19, 2018
Na<sup>+</sup> , K<sup>+</sup> -ATPase activity in children with autism spectrum disorder: Searching for the reason(s) of its decrease in blood cellsAlessandra Bolotta, Paola Visconti, Giorgio Fedrizzi, et al.
Oxidative Medicine and Cellular Longevity|January 5, 2019
Oxidative Stress in Autistic Children Alters Erythrocyte Shape in the Absence of Quantitative Protein Alterations and of Loss of Membrane Phospholipid AsymmetryAlessandra Bolotta, Michela Battistelli, Elisabetta Falcieri, et al.
Brain Sciences|October 21, 2020
Brain Magnetic Resonance Findings in 117 Children with Autism Spectrum Disorder under 5 Years OldMagali Jane Rochat, Giacomo Distefano, Monica Maffei, et al.
Molecular Autism|February 27, 2018
Advanced glycation endproducts, dityrosine and arginine transporter dysfunction in autism - a source of biomarkers for clinical diagnosisAttia Anwar, Provvidenza Maria Abruzzo, Sabah Pasha, et al.
Frontiers in Psychiatry|March 30, 2022
Contribution of <i>CACNA1H</i> Variants in Autism Spectrum Disorder SusceptibilityMarta Viggiano, Tiziano D'Andrea, Cinzia Cameli, et al.
Scientific Reports|August 31, 2017
High predictive values of RBC membrane-based diagnostics by biophotonics in an integrated approach for Autism Spectrum DisordersGiorgia Giacometti, Carla Ferreri, Anna Sansone, et al.
Neurology|March 6, 2016
The syndrome of polymicrogyria, thalamic hypoplasia, and epilepsy with CSWSEmanuele Bartolini, Melania Falchi, Francesco Zellini, et al.
Research Square|November 14, 2023
Whole genome analysis of rare deleterious variants adds further evidence to BRSK2 and other risk genes in Autism Spectrum DisorderElena Bacchelli, Marta Viggiano, Fabiola Ceroni, et al.
NPJ Genomic Medicine|March 23, 2024
Genomic analysis of 116 autism families strengthens known risk genes and highlights promising candidatesMarta Viggiano, Fabiola Ceroni, Paola Visconti, et al.
Journal of Cellular and Molecular Medicine|January 21, 2021
An increased burden of rare exonic variants in NRXN1 microdeletion carriers is likely to enhance the penetrance for autism spectrum disorderCinzia Cameli, Marta Viggiano, Magali J Rochat, et al.
Pageof 6