Conglei Song
Hefei, China
Last Updated: 09/26/2026
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Found 8 publications
Clinical and Genetic Characterization of Inherited NPRL3 Splice Variants in Two Patients With Epilepsy.
Journal: Molecular genetics & genomic medicine
Published: February 12, 2026
Correction: SPOUT1 variants associated with autosomal-recessive developmental and epileptic encephalopathy.
Journal: Acta epileptologica
Published: September 12, 2025
Clinical characteristics and treatment of two children with Lesch-Nyhan syndrome
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: August 05, 2025
Chinese Family With Knobloch Syndrome Associated With a Novel PAK2 Variant Leading to Reduced Phosphorylation Levels.
Journal: Molecular genetics & genomic medicine
Published: January 07, 2025
SPOUT1 variants associated with autosomal-recessive developmental and epileptic encephalopathy.
Journal: Acta epileptologica
Published: May 18, 2024
QSOX1 exerts anti-inflammatory effects in sepsis-induced acute lung injury: Regulation involving EGFR phosphorylation mediated M1 polarization of macrophages.
Journal: The international journal of biochemistry & cell biology
Published: April 15, 2024
Whole-exome Sequencing Helps the Diagnosis and Treatment in Children with Neurodevelopmental Delay Accompanied Unexplained Dyspnea.
Journal: Scientific reports
Published: September 18, 2017
Effects of different sedation regimens on sedation and inflammatory response in critically ill children with multiple trauma
Journal: Zhonghua wei zhong bing ji jiu yi xue
Published: June 20, 2017
Showing 1-8 of 8
Last Updated: 09/26/2026