Chengqing Yang
No. 1677 Wutaishan Road
Qingdao, 266000, China
Qingdao, 266000, China
Last Updated: 09/26/2026
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Found 27 publications
Case Report: Long-term follow-up of a schoolboy with Gitelman syndrome and epilepsy-causation or coincidence?
Journal: Frontiers in pediatrics
Published: December 22, 2025
A pediatric patient with Warsaw breakage syndrome presenting with epilepsy: a case report and literature review.
Journal: Frontiers in neuroscience
Published: December 02, 2025
A patient with a PTPN11 gene variant complicated with Chiari I malformation and syringomyelia and a review of literatures.
Journal: International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience
Published: July 21, 2024
A rare pediatric patient of anti-IgLON5 encephalitis with epileptic seizures as the first symptom.
Journal: International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience
Published: March 28, 2024
A case of variant of GBS with positive serum ganglioside GD3 IgG antibody.
Journal: Italian journal of pediatrics
Published: May 10, 2023
TMEM173 rs7447927 genetic polymorphism and susceptibility to severe enterovirus 71 infection in Chinese children.
Journal: Immunity, inflammation and disease
Published: July 13, 2022
Guillain-Barré syndrome with unilateral peripheral facial paralysis in a Chinese child.
Journal: International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience
Published: May 12, 2022
Association of the IRAK4 rs4251545 genetic polymorphism with severity of enterovirus-71 infection in Chinese children.
Journal: Immunity, inflammation and disease
Published: December 28, 2021
Whole-exome sequencing analysis to identify novel potential pathogenetic NPC1 mutations in two Chinese families with Niemann-Pick disease type C.
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: October 04, 2021
A novel de novo frameshift variation in the SON gene causing severe global developmental delay and seizures in a Chinese female.
Journal: International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience
Published: September 02, 2021
Last Updated: 09/26/2026