Baiyu Chen

Changsha, 410008, China

Last Updated: 09/26/2026

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Found 16 publications

Mitochondrial and lysosomal dysfunctions might be involved in the pathogenesis of the CACNA1A-related neurodevelopmental disorders according to in vitro studies.

Mitochondrial and lysosomal dysfunctions might be involved in the pathogenesis of the CACNA1A-related neurodevelopmental disorders according to in vitro studies.

Journal: Biological research

Published: August 31, 2025

The genotype-phenotype correlations of the CACNA1A-related neurodevelopmental disorders: a small case series and literature reviews.

The genotype-phenotype correlations of the CACNA1A-related neurodevelopmental disorders: a small case series and literature reviews.

Journal: Frontiers in molecular neuroscience

Published: May 14, 2023

Disruption of mitochondrial and lysosomal functions by human CACNA1C variants expressed in HEK 293 and CHO cells.

Disruption of mitochondrial and lysosomal functions by human CACNA1C variants expressed in HEK 293 and CHO cells.

Journal: Frontiers in molecular neuroscience

Published: April 21, 2023

Pediatric Ocular Myasthenia Gravis: Single-Center Experience.

Pediatric Ocular Myasthenia Gravis: Single-Center Experience.

Journal: Pediatric neurology

Published: February 20, 2023

Genotype-phenotype correlations of STXBP1 pathogenic variants and the treatment choices for STXBP1-related disorders in China.

Genotype-phenotype correlations of STXBP1 pathogenic variants and the treatment choices for STXBP1-related disorders in China.

Journal: BMC medical genomics

Published: September 14, 2022

Attention-deficit/hyperactive disorder updates.

Attention-deficit/hyperactive disorder updates.

Journal: Frontiers in molecular neuroscience

Published: April 21, 2022

A novel KCNQ2 missense variant in non-syndromic intellectual disability causes mild gain-of-function of Kv7.2 channel.

A novel KCNQ2 missense variant in non-syndromic intellectual disability causes mild gain-of-function of Kv7.2 channel.

Journal: Clinica chimica acta; international journal of clinical chemistry

Published: February 02, 2022

The Contribution of HCN Channelopathies in Different Epileptic Syndromes, Mechanisms, Modulators, and Potential Treatment Targets: A Systematic Review.

The Contribution of HCN Channelopathies in Different Epileptic Syndromes, Mechanisms, Modulators, and Potential Treatment Targets: A Systematic Review.

Journal: Frontiers in molecular neuroscience

Published: November 01, 2021

Urine Organic Acids as Metabolic Indicators for Global Developmental Delay/Intellectual Disability in Chinese Children.

Urine Organic Acids as Metabolic Indicators for Global Developmental Delay/Intellectual Disability in Chinese Children.

Journal: Frontiers in molecular biosciences

Published: October 22, 2021

Autism spectrum disorder and comorbid neurodevelopmental disorders (ASD-NDDs): Clinical and genetic profile of a pediatric cohort.

Autism spectrum disorder and comorbid neurodevelopmental disorders (ASD-NDDs): Clinical and genetic profile of a pediatric cohort.

Journal: Clinica chimica acta; international journal of clinical chemistry

Published: August 11, 2021

Correlation Analyses of Clinical Manifestations and Variant Effects in KCNB1-Related Neurodevelopmental Disorder.

Correlation Analyses of Clinical Manifestations and Variant Effects in KCNB1-Related Neurodevelopmental Disorder.

Journal: Frontiers in pediatrics

Published: August 08, 2021

Treatment for the Benign Childhood Epilepsy With Centrotemporal Spikes: A Monocentric Study.

Treatment for the Benign Childhood Epilepsy With Centrotemporal Spikes: A Monocentric Study.

Journal: Frontiers in neurology

Published: February 22, 2021

Showing 1-12 of 16

Last Updated: 09/26/2026