Search Results - "Neurodevelopmental disorder"

Association between neonatal jaundice and autism spectrum disorders among children: a meta-analysis by Ensiyeh Jenabi, Saeid Bashirian, Salman Khazaei

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Brain Connectivity in Autism by Lucina Q. Uddin

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Subclinical Inflammatory Status in Rett Syndrome by Alessio Cortelazzo, Claudio De Felice, Roberto Guerranti, Cinzia Signorini, Silvia Leoncini, Alessandra Pecorelli, Gloria Zollo, Claudia Landi, Giuseppe Valacchi, Lucia Ciccoli, Luca Bini, Joussef Hayek

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Cytogenetic analysis of autistic children with down syndrome features by Rajat Hegde, Smita Hegde, Pooja Joshi, Santoshkumar Gataraddi, Sujayendra Kulkarni, Gurushantappa Kadkol, Suyamindra S Kulkarni, Kusal K Das, Pramod B Gai

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Prevalence, Incidence, and Surgical Treatment Trends of Cerebral Palsy across Türkiye: A Nationwide Cohort Study by İzzet Özay Subaşi, İzzet Bingöl, Niyazi Erdem Yaşar, Ebru Dumlupinar, Naim Ata, M. Mahir Ülgü, Şuayip Birinci, Mustafa Okan Ayvali, Serkan Erkuş, Mehmet Salih Söylemez, Güzelali Özdemir

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Williams-Beuren Syndrome: A Case Report by Seren Kaya, Kaan Orhan, Firdevs Tulga Öz

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Body mass index changes in children and adolescents with intelectual disability during the COVID-19 pandemic by Nika Šuc, Blaž Lešnik

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Dietary Management for Adolescents with Prader–Willi Syndrome by Miller JL, Tan M

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Could Cariprazine Be a Possible Choice for High Functioning Autism? A Case Report by Andrea Miuli, Carlotta Marrangone, Ornella Di Marco, Arianna Pasino, Gianfranco Stigliano, Alessio Mosca, Mauro Pettorruso, Fabrizio Schifano, Giovanni Martinotti

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Effect of a Memory Rehabilitation Program on Executive Functions of Children With Attention Deficit/Hyperactivity Disorder by Fatemeh Jafari Nodoushan, Hasan Zare Khormizi

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Effects of ω-3 PUFAs Supplementation on Myocardial Function and Oxidative Stress Markers in Typical Rett Syndrome by Silvia Maffei, Claudio De Felice, Pierpaolo Cannarile, Silvia Leoncini, Cinzia Signorini, Alessandra Pecorelli, Barbara Montomoli, Stefano Lunghetti, Lucia Ciccoli, Thierry Durand, Roberto Favilli, Joussef Hayek

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DNA Methylation in <i>LIME1</i> and <i>SPTBN2</i> Genes Is Associated with Attention Deficit in Children by Sung-Chou Li, Ho-Chang Kuo, Lien-Hung Huang, Wen-Jiun Chou, Sheng-Yu Lee, Wen-Ching Chan, Liang-Jen Wang

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Quantitative Identification of ADHD Tendency in Children With Immersive Fingertip Force Control Tasks by Zhihao Zhang, Simin Kang, Jifan Yu, Heyang Li, Gaohan Yin, Hongxing Zhang, Li Sun, Dangxiao Wang

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Association between assisted reproductive technology and autism spectrum disorders in Iran: a case-control study by Ensiyeh Jenabi, Mahdieh Seyedi, Ronak Hamzehei, Saeid Bashirian, Mohammad Rezaei, Katayoon Razjouyan, Salman Khazaei

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Persistent Unresolved Inflammation in the Mecp2-308 Female Mutated Mouse Model of Rett Syndrome by Alessio Cortelazzo, Claudio De Felice, Bianca De Filippis, Laura Ricceri, Giovanni Laviola, Silvia Leoncini, Cinzia Signorini, Monica Pescaglini, Roberto Guerranti, Anna Maria Timperio, Lello Zolla, Lucia Ciccoli, Joussef Hayek

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A small-molecule TrkB ligand restores hippocampal synaptic plasticity and object location memory in Rett syndrome mice by Wei Li, Alba Bellot-Saez, Mary L. Phillips, Tao Yang, Frank M. Longo, Lucas Pozzo-Miller

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Salubrious effects of proanthocyanidins on behavioral phenotypes and DNA repair deficiency in the BTBR mouse model of autism by Abdulelah F. Alhusain, Mohamed A. Mahmoud, Hussain N. Alhamami, Saad Ebrahim Alobid, Mushtaq A. Ansari, Sheikh F. Ahmad, Ahmed Nadeem, Saleh A. Bakheet, Gamaleldin I. Harisa, Sabry M. Attia

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Dietary cholesterol supplementation and inhibitory factor 1 serum levels in two dizygotic Smith-Lemli-Opitz syndrome twins: a case report by Maurizio Delvecchio, Biagio Rapone, Simonetta Simonetti, Simona Fecarotta, Graziana De Carlo, Elvira Favoino, Maria Teresa Loverro, Anna Maria Isdraele Romano, Federica Taurino, Edoardo Di Naro, Antonio Gnoni

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The views and knowledge of parents of children with autism spectrum disorder on a range of treatments by V Wetherston, S Gangat, N Shange, K Wheeler, S B Sayed Karrim, J Pahl

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Clinical and Genetic Study on a Chinese Patient with Infantile Onset Epileptic Encephalopathy carrying a PPP3CA Null Variant: a case report by Sai Yang, Xiang Shen, Qingyun Kang, Xiaojun Kuang, Zeshu Ning, Shulei Liu, Hongmei Liao, Zhenhua Cao, Liming Yang

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