Qiuxia Chen
Nanjing, China
Last Updated: 09/26/2026
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Found 10 publications
COQ2-Associated Primary Coenzyme Q10 Deficiency Presenting With Proteinuria: A Case Report and Literature Review.
Journal: Molecular genetics & genomic medicine
Published: December 12, 2025
Monogenic Causes Identified in 23.68% of Children with Steroid-Resistant Nephrotic Syndrome: A Single-Centre Study.
Journal: Kidney diseases (Basel, Switzerland)
Published: July 08, 2023
Functional Characterization of PHEX Gene Variants in Children With X-Linked Hypophosphatemic Rickets Shows No Evidence of Genotype-Phenotype Correlation.
Journal: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
Published: December 04, 2019
Whole-genome sequencing revealed an interstitial deletion encompassing OCRL and SMARCA1 gene in a patient with Lowe syndrome.
Journal: Molecular genetics & genomic medicine
Published: January 13, 2019
PEA3 protects against gentamicin nephrotoxicity: role of mitochondrial dysfunction.
Journal: American journal of translational research
Published: December 28, 2016
COX-2/mPGES-1/PGE2 cascade activation mediates uric acid-induced mesangial cell proliferation.
Journal: Oncotarget
Published: October 11, 2016
Diagnosis of cobalamin C deficiency with renal abnormality from onset in a Chinese child by next generation sequencing: A case report.
Journal: Experimental and therapeutic medicine
Published: September 26, 2016
A case of Lowe syndrome
Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics
Published: January 14, 2016
Showing 1-10 of 10
Last Updated: 09/26/2026