Chengyan Y. Li
No. 57, South Renmin Avenue
Zhanjiang, 524001, China
Zhanjiang, 524001, China
Last Updated: 09/26/2026
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Found 15 publications
Clinical and genetic analysis of a Chinese pedigree affected with Charcot-Marie-Tooth disease presenting as childhood-onset encephalopathy
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: May 06, 2026
Clinical phenotype and genetic analysis of a child with Cortical dysplasia, complex, with other brain malformations 4 and epilepsy due to a TUBG1 gene variant
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: October 10, 2025
Transcription factor EB improves hypoxic pulmonary hypertension in fetal rats by suppressing NLRP3 inflammasome activation via induction of mitophagy.
Journal: Scientific reports
Published: March 31, 2025
Reconstruction of hands and feet defects with medial sural artery perforator (MSAP) flap and MSAP fascial flap: A comparative study.
Journal: Annales de chirurgie plastique et esthetique
Published: February 03, 2025
Clinical phenotype and genetic analysis of a child with Intellectual developmental disorder and epilepsy due to variant of CLTC gene
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: July 01, 2024
Trio-whole exome sequencing reveals the importance of de novo variants in children with intellectual disability and developmental delay.
Journal: Scientific reports
Published: March 11, 2024
Clinical and genetic characteristics of a child with Developmental and epileptic encephalopathy 104 due to variant of ATP6V0A1 gene
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: March 06, 2024
Clinical and genetic analysis of three children with Menkes disease due to variants of ATP7A gene
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: May 22, 2023
Silencing LCN2 enhances RSL3-induced ferroptosis in T cell acute lymphoblastic leukemia.
Journal: Gene
Published: April 20, 2023
A case of neurodevelopmental disorder with refractory epilepsy caused by GRIA2 gene variant
Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics
Published: November 01, 2022
Ketogenic Diet Attenuates Refractory Epilepsy of Harel-Yoon Syndrome With ATAD3A Variants: A Case Report and Review of Literature.
Journal: Pediatric neurology
Published: October 20, 2022
Last Updated: 09/26/2026