Skip to main content

and
Your search also matched 3 preview-only Content is preview-only when you or your institution have not yet subscribed to it.

By making our abstracts and previews universally accessible we help you purchase only the content that is relevant to you.
results, e.g.

Spatial and temporal correlations of spike trains in frog retinal ganglion cells

Include preview-only content
  1. Article

    Open Access

    Developmental change of brain volume in Rett syndrome in Taiwan

    Rett syndrome (RTT) is characterized by neurological regression. This pioneering study investigated the effect of age on brain volume reduction by analyzing magnetic resonance imaging findings in participants ...

    Tz-Yun Jan, Lee-Chin Wong, Chia-Jui Hsu in Journal of Neurodevelopmental Disorders (2024)

  2. Article

    Open Access

    Developmental milestones and daily living skills in individuals with Angelman syndrome

    Angelman syndrome (AS) is a neurodevelopmental disorder associated with severe global developmental delay. However, the ages at which different developmental skills are achieved in these individuals remain unc...

    Anjali Sadhwani, Sonya Powers, Anne Wheeler in Journal of Neurodevelopmental Disorders (2024)

  3. Article

    Open Access

    The microstructural change of the brain and its clinical severity association in pediatric Tourette syndrome patients

    Gilles de la Tourette syndrome (GTS) is a prevalent pediatric neurological disorder. Most studies point to abnormalities in the cortico-striato-thalamocortical (CSTC) circuits. Neuroimaging studies have shown ...

    Chia-Jui Hsu, Lee Chin Wong, Hsin-Pei Wang in Journal of Neurodevelopmental Disorders (2023)

  4. Article

    Open Access

    Enabling endpoint development for interventional clinical trials in individuals with Angelman syndrome: a prospective, longitudinal, observational clinical study (FREESIAS)

    Angelman syndrome (AS) is a rare neurodevelopmental disorder characterized by the absence of a functional UBE3A gene, which causes developmental, behavioral, and medical challenges. While currently untreatable, c...

    Jorrit Tjeertes, Carlos A. Bacino in Journal of Neurodevelopmental Disorders (2023)

  5. Article

    Open Access

    Firing activity of locus coeruleus noradrenergic neurons decreases in necdin-deficient mice, an animal model of Prader–Willi syndrome

    Prader–Willi syndrome (PWS) is a neurodevelopmental disorder characterized by multiple respiratory, cognitive, endocrine, and behavioral symptoms, such as central apnea, intellectual disabilities, exaggerated ...

    Rui-Ni Wu, Wei-Chen Hung, Ching-Tsuey Chen in Journal of Neurodevelopmental Disorders (2020)

  6. Article

    Open Access

    Few individuals with Lennox-Gastaut syndrome have autism spectrum disorder: a comparison with Dravet syndrome

    Autism spectrum disorder (ASD) in epilepsy has been a topic of increasing interest, which in general occurs in 15–35% of the patients with epilepsy, more frequently in those with intellectual disability (ID). ...

    Na He, Bing-Mei Li, Zhao-**a Li, Jie Wang in Journal of Neurodevelopmental Disorders (2018)

  7. Article

    Open Access

    Role of type-specific neuron properties in a spinal cord motor network

    Recent recordings from spinal neurons in hatchling frog tadpoles allow their type-specific properties to be defined. Seven main types of neuron involved in the control of swimming have been characterized. To i...

    Bart Sautois, Stephen R. Soffe, Wen-Chang Li in Journal of Computational Neuroscience (2007)