Search Results - "neurodevelopmental"

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

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The role of parenting stress in anxiety and sleep outcomes in toddlers with congenital heart disease by Charles Lepage, Charles Lepage, Isabelle Gaudet, Isabelle Gaudet, Amélie Doussau, Marie-Claude Vinay, Charlotte Gagner, Zorina von Siebenthal, Nancy Poirier, Nancy Poirier, Nancy Poirier, Marie-Noëlle Simard, Marie-Noëlle Simard, Natacha Paquette, Natacha Paquette, Anne Gallagher, Anne Gallagher

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Association between maternal shift work during pregnancy child overweight and metabolic outcomes in early childhood by Che-Wei Liao, Che-Wei Liao, Chih-Fu Wei, Mei-Huei Chen, Mei-Huei Chen, Wu-Shiun Hsieh, Wu-Shiun Hsieh, Ching-Chun Lin, Pau-Chung Chen, Pau-Chung Chen, Pau-Chung Chen, Pau-Chung Chen

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Epidemiology, risk factors and outcomes associated with candidaemia in very low birth weight infants at a tertiary South African Hospital over a 7-year period (2013-2019) by Tanusha D. Ramdin, Vindana Chibabhai, Robin T. Saggers, Rossella M. Bandini, Daynia E. Ballot

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Prediction of Delayed Neurodevelopment in Infants Using Brainstem Auditory Evoked Potentials and the Bayley II Scales by Xiaoyan Wang, Xianming Carroll, Hong Wang, Ping Zhang, Jonathan Nimal Selvaraj, Sandra Leeper-Woodford

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Registry of Compartmental Ephrin-B3 Guidance Patterns With Respect to Emerging Multimodal Midbrain Maps by Jeremiah P. C. Stinson, Cooper A. Brett, Julianne B. Carroll, Mark L. Gabriele

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Modulation of Brain Cholesterol Metabolism through CYP46A1 Overexpression for Rett Syndrome by Emilie Audouard, Nicolas Khefif, Béatrix Gillet-Legrand, Fanny Nobilleau, Ouafa Bouazizi, Serena Stanga, Gaëtan Despres, Sandro Alves, Antonin Lamazière, Nathalie Cartier, Françoise Piguet

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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

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Restoration of motor learning in a mouse model of Rett syndrome following long-term treatment with a novel small-molecule activator of TrkB by Ian Adams, Tao Yang, Frank M. Longo, David M. Katz

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Novel mutations in PANK2 and PLA2G6 genes in patients with neurodegenerative disorders: two case reports by Hassan Dastsooz, Hamid Nemati, Mohammad Ali Farazi Fard, Majid Fardaei, Mohammad Ali Faghihi

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Neonatal risk factors associated with autism spectrum disorders: an umbrella review by Amir Mohammad Salehi, Erfan Ayubi, Salman Khazaei, Ensiyeh Jenabi, Saeid Bashirian, Zohreh Salimi

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Xp22.31 copy number variations in 87 fetuses: refined genotype-phenotype correlations by prenatal and postnatal follow-up by Huamei Hu, Yulin Huang, Renke Hou, Huanhuan Xu, Yalan Liu, Xueqian Liao, Juchun Xu, Lupin Jiang, Dan Wang

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Effect of Transcranial Direct Current Stimulation on Impulsivity and Aggression in Elementary School Students With Dyslexia: A Randomized Clinical Trial by Haniyeh Gholamzade Nikjoo, Marziyeh Alivandi Vafa, Seyed Mahmoud Tabatabaei, Naiemeh Moheb

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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

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Association between polymorphisms in the GRIN1 gene 5' regulatory region and schizophrenia in a northern Han Chinese population and haplotype effects on protein expression in vitro by Yong-ping Liu, Mei Ding, Xi-cen Zhang, Yi Liu, Jin-feng Xuan, Jia-xin Xing, Xi Xia, Jun Yao, Bao-jie Wang

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Roles of caregiver-child interaction on the association of socioeconomic status with early childhood development: a population-based study in rural China by Rui Chang, Chunan Li, Mengna Wei, Yanfen Jiang, Jianduan Zhang

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Effect of a nonsurgical treatment program on the gait pattern of idiopathic toe walking: a case report by Szopa A, Domagalska˗Szopa M, Gallert˗Kopyto W, Kiebzak W, Plinta R

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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

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Evaluating the serum levels of zinc, copper, magnesium, and 25-hydroxy vitamin D in children with idiopathic drug-resistant epilepsy; a cross-sectional study by Azita Tavasoli, Ladan Afsharkhas, Behnaz Parvini

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Overelaborated synaptic architecture and reduced synaptomatrix glycosylation in a Drosophila classic galactosemia disease model by Patricia Jumbo-Lucioni, William Parkinson, Kendal Broadie

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