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Human Molecular Genetics|September 15, 2022
Analysis for variable manifestations and molecular characteristics of pyridox(am)ine-5'-phosphate oxidase (PNPO) deficiencyXianru Jiao, Pan Gong, Yue Niu, et al.
Frontiers in Neurology|August 29, 2022
Genetic and phenotypic spectrum of Chinese patients with epilepsy and photosensitivityYue Niu, Pan Gong, Xianru Jiao, et al.
Frontiers in Neurology|November 22, 2021
De Novo Variants in the DYNC1H1 Gene Associated With Infantile SpasmsHaipo Yang, Pan Gong, Xianru Jiao, et al.
Frontiers in Neurology|June 1, 2022
The Clinical Features and Long-Term Follow-Up of Vitamin B6-Responsive Infantile Spasms in a Chinese CohortXianru Jiao, Pan Gong, Yue Niu, et al.
Scientific Reports|August 6, 2021
The relationship between the characteristics of burst suppression pattern and different etiologies in epilepsyHaipo Yang, Pan Gong, Xianru Jiao, et al.
Human Mutation|January 11, 2022
Novel biallelic loss of EEF1B2 function links to autosomal recessive intellectual disabilityPan Gong, Jing Liu, Xianru Jiao, et al.
Developmental Medicine and Child Neurology|November 19, 2019
Clinical and genetic features in pyridoxine-dependent epilepsy: a Chinese cohort studyXianru Jiao, Jiao Xue, Pan Gong, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|June 1, 2024
A generalized seizure type: Myoclonic-to-tonic seizureZongpu Zhou, Pan Gong, Xianru Jiao, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 19, 2025
Interictal paroxysmal fast activity and functional connectivity in steroid responsive and non-responsive Lennox-Gastaut syndromeZongpu Zhou, Pan Gong, Xianru Jiao, et al.
Orphanet Journal of Rare Diseases|March 30, 2020
Analyzing clinical and genetic characteristics of a cohort with multiple congenital anomalies-hypotonia-seizures syndrome (MCAHS)Xianru Jiao, Jiao Xue, Pan Gong, et al.
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