Shuang-zhu Lin
Changchun, China
Last Updated: 09/26/2026
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Found 16 publications
A case of childhood hyperekplexia due to a novel nonsense variant in the GLRA1 gene.
Journal: Medicine
Published: August 06, 2025
Eosinophilic granuloma of the clavicle in an 11-year-old Chinese girl: A case report.
Journal: Medicine
Published: June 30, 2023
A case of West syndrome and global developmental delay in a child with a heterozygous mutation in the TBL1XR1 gene: A case report.
Journal: Medicine
Published: May 12, 2023
A randomized, double-blind, placebo-controlled multicenter clinical trial of Xiehuang Jiejing granule in the treatment of cough variant asthma in children.
Journal: Medicine
Published: November 19, 2022
Children with infectious pneumonia caused by Ralstonia insidiosa: A case report.
Journal: World journal of clinical cases
Published: November 08, 2022
Aicardi-Goutières syndrome type 7 in a Chinese child: A case report.
Journal: World journal of clinical cases
Published: August 13, 2022
Retroperitoneal leiomyoma located in the broad ligament: A case report.
Journal: World journal of clinical cases
Published: August 04, 2022
Novel compound heterozygous variants in the LHX3 gene caused combined pituitary hormone deficiency: A case report.
Journal: World journal of clinical cases
Published: April 15, 2022
Two novel mutations in the VPS33B gene in a Chinese patient with arthrogryposis, renal dysfunction and cholestasis syndrome 1: A case report.
Journal: World journal of clinical cases
Published: April 13, 2022
VARS2 gene mutation leading to overall developmental delay in a child with epilepsy: A case report.
Journal: World journal of clinical cases
Published: March 25, 2022
Novel frameshift mutation in the AHDC1 gene in a Chinese global developmental delay patient: A case report.
Journal: World journal of clinical cases
Published: December 21, 2021
Last Updated: 09/26/2026