Jiaoe Gong

Changsha, 410013, China

Last Updated: 09/26/2026

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Found 11 publications

Pathogens analysis and modeling of mortality risk in sepsis patients with COVID-19 and without COVID-19.

Pathogens analysis and modeling of mortality risk in sepsis patients with COVID-19 and without COVID-19.

Journal: Scientific reports

Published: December 23, 2025

Unraveling the Neural Circuits: Techniques, Opportunities and Challenges in Epilepsy Research.

Unraveling the Neural Circuits: Techniques, Opportunities and Challenges in Epilepsy Research.

Journal: Cellular and molecular neurobiology

Published: December 25, 2023

Clinical characteristics and genetic analysis of a case of infantile Schaaf-Yang syndrome due to a heterozygous variant of MAGEL2 gene

Clinical characteristics and genetic analysis of a case of infantile Schaaf-Yang syndrome due to a heterozygous variant of MAGEL2 gene

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: September 20, 2023

Metabotropic glutamate receptors (mGluRs) in epileptogenesis: an update on abnormal mGluRs signaling and its therapeutic implications.

Metabotropic glutamate receptors (mGluRs) in epileptogenesis: an update on abnormal mGluRs signaling and its therapeutic implications.

Journal: Neural regeneration research

Published: July 25, 2023

Radiosensitizer EXO-miR-197-3p Inhibits Nasopharyngeal Carcinoma Progression and Radioresistance by Regulating the AKT/mTOR Axis and HSPA5-mediated Autophagy.

Radiosensitizer EXO-miR-197-3p Inhibits Nasopharyngeal Carcinoma Progression and Radioresistance by Regulating the AKT/mTOR Axis and HSPA5-mediated Autophagy.

Journal: International journal of biological sciences

Published: December 10, 2021

Expansion of Clinical and Genetic Spectrum of DDX3X Neurodevelopmental Disorder in 23 Chinese Patients.

Expansion of Clinical and Genetic Spectrum of DDX3X Neurodevelopmental Disorder in 23 Chinese Patients.

Journal: Frontiers in molecular neuroscience

Published: October 11, 2021

Genetic screening in patients of Meige syndrome and blepharospasm.

Genetic screening in patients of Meige syndrome and blepharospasm.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Published: July 25, 2021

The second DDOST-CDG patient with lactose intolerance, developmental delay, and situs inversus totalis.

The second DDOST-CDG patient with lactose intolerance, developmental delay, and situs inversus totalis.

Journal: Journal of human genetics

Published: June 22, 2021

Cohen syndrome in two patients from China.

Cohen syndrome in two patients from China.

Journal: Molecular genetics & genomic medicine

Published: March 01, 2021

Rare Meningitis and Epileptic Seizure Infected with Brucella melitensis: a Case Report.

Rare Meningitis and Epileptic Seizure Infected with Brucella melitensis: a Case Report.

Journal: Clinical laboratory

Published: November 12, 2019

Neurological complications and risk factors of cardiopulmonary failure of EV-A71-related hand, foot and mouth disease.

Neurological complications and risk factors of cardiopulmonary failure of EV-A71-related hand, foot and mouth disease.

Journal: Scientific reports

Published: October 22, 2014

Showing 1-11 of 11

Last Updated: 09/26/2026