Qin Wang
139 Middle Renmin Road
Changsha, 410011, China
Changsha, 410011, China
Last Updated: 09/26/2026
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Found 68 publications
Dent Disease 1 Associated with a Rare Novel Renal Chloride Channel 5 Variant in a Chinese Family.
Journal: DNA and cell biology
Published: April 06, 2026
Surgical treatment of Meniere's disease
Journal: Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery
Published: March 16, 2026
Natural history and phenotype-genotype correlations in GJB2-related hearing loss: a systematic and comprehensive review.
Journal: Journal of genetics and genomics = Yi chuan xue bao
Published: December 18, 2025
Joint association of estimated skeletal muscle mass index and prognostic nutritional index with all-cause mortality in individuals with non-metastatic nasopharyngeal cancer.
Journal: Frontiers in nutrition
Published: December 16, 2025
Multicentre gene therapy for OTOF-related deafness followed up to 2.5 years.
Journal: Nature
Published: September 14, 2025
Correlation analysis between endolymphatic hydrops severity and high jugular bulb with vestibular function in refractory Ménière's disease patients
Journal: Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery
Published: August 26, 2025
International expert consensus on gene therapy for hereditary hearing loss: Based on clinical trials.
Journal: Med (New York, N.Y.)
Published: July 22, 2025
Clinical gene therapy restores hearing: a paradigm shift.
Journal: Trends in molecular medicine
Published: May 18, 2025
A case of extensive myelinated retinal nerve fibers combined with macular hole retinal detachment.
Journal: International ophthalmology
Published: February 17, 2025
Long-term vestibular and audiometric results in meniere's patients following endolymphatic duct blockage, sac drainage or sac decompression.
Journal: European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery
Published: January 14, 2025
Rare SRRM2 mutation in neurodevelopmental disorders involving hyperphagia triggering severe obesity and other complication.
Journal: Frontiers in medicine
Published: December 23, 2024
Last Updated: 09/26/2026