Search Results - "Neurodevelopmental disorder"

Long-lasting alterations to DNA methylation and ncRNAs could underlie the effects of fetal alcohol exposure in mice by Benjamin I. Laufer, Katarzyna Mantha, Morgan L. Kleiber, Eric J. Diehl, Sean M. F. Addison, Shiva M. Singh

Connect to this object online.

Peroxisome proliferator-activated receptor alpha plays a crucial role in behavioral repetition and cognitive flexibility in mice by Giuseppe D'Agostino, Claudia Cristiano, David J. Lyons, Rita Citraro, Emilio Russo, Carmen Avagliano, Roberto Russo, Giuseppina Mattace Raso, Rosaria Meli, Giovambattista De Sarro, Lora K. Heisler, Antonio Calignano

Connect to this object online.

Fraternal twins with Phelan-McDermid syndrome not involving the SHANK3 gene: case report and literature review by Shan Li, Ke-wang Xi, Ting Liu, Ying Zhang, Meng Zhang, Li-dong Zeng, Juan Li

Connect to this object online.

Application of chromosome microarray analysis and karyotyping in diagnostic assessment of abnormal Down syndrome screening results by Han Kang, Lingxi Wang, Xingyu Li, Chonglan Gao, Yamei Xie, Yu Hu

Connect to this object online.

Trajectories of children and adolescents attending a psychiatric emergency unit during the COVID-19 confinements: 2020-2022 longitudinal study by Marina Adrados-Pérez, Vicent Llorca-Bofí, María Mur Laín, Carla Albert Porcar, Eugènia Nicolau-Subires, Lucía Ibarra-Pertusa, Andrea Jiménez-Mayoral, Esther Buil-Reiné, Filip Budny, Belén Resa-Pérez, Vanessa Gladys Velásquez-Acebey, Laura Arenas-Pijoan, María Irigoyen-Otiñano, Jorge López-Castroman

Connect to this object online.

Prioritizing a Research Agenda of Transitional Care Interventions for Childhood-Onset Disabilities by Andrea Duncan, Andrea Duncan, Dorothy Luong, Laure Perrier, Mark T. Bayley, Mark T. Bayley, Mark T. Bayley, Gail Andrew, Kelly Arbour-Nicitopoulos, Kelly Arbour-Nicitopoulos, Brian Chan, Brian Chan, C. J. Curran, Gina Dimitropoulos, Laura Hartman, Lennox Huang, Lennox Huang, Monika Kastner, Monika Kastner, Monika Kastner, Shauna Kingsnorth, Shauna Kingsnorth, Anna McCormick, Anna McCormick, Michelle Nelson, Michelle Nelson, David Nicholas, Melanie Penner, Melanie Penner, Melanie Penner, Laura Thompson, Alene Toulany, Alene Toulany, Amanda Woo, Joanne Zee, Joanne Zee, Sarah E. P. Munce, Sarah E. P. Munce, Sarah E. P. Munce

Connect to this object online.

Novel MEF2C point mutations in Chinese patients with Rett (−like) syndrome or non-syndromic intellectual disability: insights into genotype-phenotype correlation by Jiaping Wang, Qingping Zhang, Yan Chen, Shujie Yu, Xiru Wu, Xinhua Bao, Yongxin Wen

Connect to this object online.

Access to child developmental assessment services in culturally and linguistically diverse metropolitan Sydney: a retrospective cohort analysis by Sibella E. Bentley, Pankaj Garg, Ori Gudes, Romy Hurwitz, Sinthu Vivekanandarajah, Lydia Y.L. So

Connect to this object online.

A case report of Chinese brothers with inherited <it>MECP2-</it>containing duplication: autism and intellectual disability, but not seizures or respiratory infections by Xu Xiu, Xu Qiong, Zhang Ying, Zhang Xiaodi, Cheng Tianlin, Wu Bingbing, Ding Yanhua, Lu Ping, Zheng Jingjing, Zhang Min, Qiu Zilong, Yu Xiang

Connect to this object online.

Intraventricular hemorrhage in preterm infants: risk factors and neurodevelopmental outcomes by Joana Soares Reis, Isabel Ayres Pereira, Joana Lira, Joana Silva, Márcia Gonçalves, Jacinto Torres, Joana Grenha

Connect to this object online.

Parent Communication Prompt to Increase Shared Decision-Making: A New Intervention Approach by Lauren M. Hubner, Heidi M. Feldman, Lynne C. Huffman

Connect to this object online.

Imprecision in Precision Medicine: Differential Response of a Disease-Linked GluN2A Mutant to NMDA Channel Blockers by Jenna R. Gale, Gabrielle J. Kosobucki, Karen A. Hartnett-Scott, Elias Aizenman

Connect to this object online.

Changes in UK parental mental health symptoms over 10 months of the COVID‐19 pandemic by Simona Skripkauskaite, Cathy Creswell, Adrienne Shum, Samantha Pearcey, Pete Lawrence, Helen Dodd, Polly Waite

Connect to this object online.

Rare variants in dynein heavy chain genes in two individuals with situs inversus and developmental dyslexia: a case report by Andrea Bieder, Elisabet Einarsdottir, Hans Matsson, Harriet E. Nilsson, Jesper Eisfeldt, Anca Dragomir, Martin Paucar, Tobias Granberg, Tie-Qiang Li, Anna Lindstrand, Juha Kere, Isabel Tapia-Páez

Connect to this object online.

What Components of Working Memory Are Impaired in Children with Reading and/or Mathematics Difficulties? by Rui Chen, George K. Georgiou, Peng Peng, Yuanyuan Li, Beilei Li, Jiali Wang, Sha Tao

Connect to this object online.

Chromosomal Microarray in Children With Developmental Delay: The Experience of a Tertiary Center in Korea by Eun Hye Yang, Yong Beom Shin, Soo Han Choi, Hye Won Yoo, Hye Young Kim, Min Jung Kwak, Kyung Hee Park, Mi Hye Bae, Ju Hyun Kong, Yun-Jin Lee, Sang Ook Nam, Young Mi Kim

Connect to this object online.

Mapping pathological phenotypes in Reelin mutant mice by Caterina eMichetti, Caterina eMichetti, Emilia eRomano, Emilia eRomano, Luisa eAltabella, Angela eCaruso, Angela eCaruso, Paolo eCastelluccio, Gaurav eBedse, Silvana eGaetani, Rossella eCanese, Giovanni eLaviola, Maria Luisa eScattoni

Connect to this object online.

Developing a cluster-based approach for deciphering complexity in individuals with neurodevelopmental differences by Tania Cuppens, Manpreet Kaur, Ajay A. Kumar, Julie Shatto, Andy Cheuk-Him Ng, Mickael Leclercq, Marek Z. Reformat, Arnaud Droit, Ian Dunham, François V. Bolduc, François V. Bolduc, François V. Bolduc

Connect to this object online.

Canagliflozin Ameliorates Oxidative Stress and Autistic-like Features in Valproic-Acid-Induced Autism in Rats: Comparison with Aripiprazole Action by Mohammed Moutaz Nakhal, Petrilla Jayaprakash, Salahdein Aburuz, Bassem Sadek, Amal Akour

Connect to this object online.

Clinical and molecular characterization of a transmitted reciprocal translocation t(1;12)(p32.1;q21.3) in a family co-segregating with mental retardation, language delay, and micro... by Wu Kuang-Lun, Chen Yann-Jang, Fang Jye-Siung, Liao Hsiao-Mei, Lee Kuei-Fang, Chen Chia-Hsiang

Connect to this object online.