Hong-wei Zhang
Jinan, China
Last Updated: 09/26/2026
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Found 8 publications
Variants in CSMD2 and CSMD3, genes involved in synaptogenesis, are associated with epilepsies.
Journal: Epilepsia
Published: March 17, 2025
Variants in EP400, encoding a chromatin remodeler, cause epilepsy with neurodevelopmental disorders.
Variants in EP400, encoding a chromatin remodeler, cause epilepsy with neurodevelopmental disorders.
Journal: American journal of human genetics
Published: June 18, 2024
Diagnosis and treatment recommendations for glucose transporter 1 deficiency syndrome.
Journal: World journal of pediatrics : WJP
Published: June 13, 2024
Simultaneous determination of 31 banned veterinary drugs during egg-laying period in poultry eggs by ultra performance liquid chromatography-tandem mass spectrometry
Journal: Se pu = Chinese journal of chromatography
Published: May 13, 2024
Missense variants in SLC9A6 cause partial epilepsy without neurodevelopmental delay.
Journal: Orphanet journal of rare diseases
Published: May 10, 2024
ARHGAP4 variants are associated with X-linked early-onset temporal lobe epilepsy.
Journal: World journal of pediatrics : WJP
Published: December 19, 2023
Functional peptidomics analysis of Saccharomyces pastorianus protein hydrolysates based on different enzyme treatments
Journal: Se pu = Chinese journal of chromatography
Published: November 16, 2023
Application of apparent diffusion coefficient in children aged 2-12 years with intellectual disability/global developmental delay who have normal conventional brain MRI findings
Journal: Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics
Published: June 19, 2019
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Last Updated: 09/26/2026