Changning Xie
Xiangya Road 87
Changsha, 410008, China
Changsha, 410008, China
Last Updated: 09/26/2026
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Found 10 publications
Heterozygous gain-of-function and mixed-type Kcna2 variants recapitulate SUDEP and increased cortical Npy-Npy1r signaling.
Journal: Neurobiology of disease
Published: April 01, 2026
GRIN2B-related neurodevelopmental disorders: genotype-phenotype correlations and therapeutic implications.
Journal: Orphanet journal of rare diseases
Published: February 23, 2025
Functional characterization and in vitro pharmacological rescue of a novel KCNA2 variant associated with developmental and epileptic encephalopathy.
Journal: Neuroscience
Published: February 19, 2025
Mutations in CLCN6 as a Novel Genetic Cause of Neuronal Ceroid Lipofuscinosis in Patients and a Murine Model.
Journal: Annals of neurology
Published: October 16, 2023
Roles of KCNA2 in Neurological Diseases: from Physiology to Pathology.
Journal: Molecular neurobiology
Published: March 31, 2023
Exploring the nurses' experiences in recognising and managing clinical deterioration in emergency patients: A qualitative study.
Journal: Australian critical care : official journal of the Confederation of Australian Critical Care Nurses
Published: September 20, 2022
Novel HCN1 Mutations Associated With Epilepsy and Impacts on Neuronal Excitability.
Journal: Frontiers in molecular neuroscience
Published: February 06, 2022
Home-based psychological nursing interventions for improvement of sleep quality and psychological health in patients with hypopharyngeal carcinoma undergoing surgical resections: a randomized trial.
Journal: Annals of palliative medicine
Published: October 05, 2021
Clinical Characteristics, Classification, and Management of Adult Nasopharyngolaryngeal Hemangioma.
Journal: The Laryngoscope
Published: April 08, 2021
Showing 1-10 of 10
Last Updated: 09/26/2026