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Carotid imaging changes and serum IL-1β, sICAM-1, and sVAP-1 levels in benign paroxysmal positional vertigo

Scientific reports, 2020-12, Vol.10 (1), p.21494-21494, Article 21494

2020

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Author Correction: Carotid imaging changes and serum IL-1β, sICAM-1, and sVAP-1 levels in benign paroxysmal positional vertigo

Scientific reports, 2021-03, Vol.11 (1), p.7305-7305, Article 7305

2021

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The effect of vascular risk factors on the efficacy of endolymphatic sac decompression surgery for Meniere's disease: a retrospective cohort study

Frontiers in neurology, 2023-05, Vol.14, p.1194456-1194456

2023

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Resolving the genetic heterogeneity of prelingual hearing loss within one family: Performance comparison and application of two targeted next generation sequencing approaches

Journal of human genetics, 2014-11, Vol.59 (11), p.599-607

2014

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Loss-of-Function Mutations in the PRPS1 Gene Cause a Type of Nonsyndromic X-linked Sensorineural Deafness, DFN2

American journal of human genetics, 2010, Vol.86 (1), p.65-71

2010

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Preimplantation genetic diagnosis for a Chinese family with autosomal recessive Meckel-Gruber syndrome type 3 (MKS3)

PloS one, 2013-09, Vol.8 (9), p.e73245-e73245

2013

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Identification of a Novel TECTA mutation in a Chinese DFNA8/12 family with prelingual progressive sensorineural hearing impairment

PloS one, 2013-07, Vol.8 (7), p.e70134-e70134

2013

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Novel missense mutations in MYO7A underlying postlingual high- or low-frequency non-syndromic hearing impairment in two large families from China

Journal of human genetics, 2011-01, Vol.56 (1), p.64-70

2011

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Development and validation of prediction model to estimate vertigo risk after endolymphatic sac decompression in Meniere’s disease: a retrospective cohort study

European archives of oto-rhino-laryngology, 2024-03, Vol.281 (3), p.1243-1252

2024

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Qualification of Pilots with Aero-Otitis Media After Balloon Eustachian Tuboplasty

Aerospace medicine and human performance, 2023-08, Vol.94 (8), p.629-633

2023

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Pilots' Spatial Visualization Ability Assessment Based on Virtual Reality

Aerospace medicine and human performance, 2023-06, Vol.94 (6), p.422-428

2023

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Dynamic Rabbit Model of Ear Barotrauma

Aerospace medicine and human performance, 2019-08, Vol.90 (8), p.696-702

2019

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Identification of a novel DFNA5 mutation, IVS7-2 a > G, in a Chinese family with non-syndromic sensorineural hearing loss

Acta oto-laryngologica, 2022-05, Vol.142 (5), p.448-453

2022

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A Dynamic Rabbit Model of Sinus Barotrauma and Its Related Pathology

Aerospace medicine and human performance, 2016-06, Vol.87 (6), p.521-527

2016

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Predictive accuracy of machine learning for radiation-induced temporal lobe injury in nasopharyngeal carcinoma patients: a systematic review and meta-analysis

Translational cancer research, 2023-09, Vol.12 (9), p.2361-2370

2023

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Identification of two novel missense WFS1 mutations, H696Y and R703H, in patients with non-syndromic low-frequency sensorineural hearing loss

Journal of genetics and genomics, 2011-02, Vol.38 (2), p.71-76

2011

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Novel missense mutations in MYO7A underlying postlingual high- or low-frequency non-syndromic hearing impairment in two large families from China

Journal of human genetics, 2011-01, Vol.56 (1), p.64-70

2011

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Preimplantation Genetic Diagnosis for a Chinese Family with Autosomal Recessive Meckel-Gruber Syndrome Type 3 (MKS3): e73245

PloS one, 2013-09, Vol.8 (9)

2013

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Identification of a Novel TECTA Mutation in a Chinese DFNA8/12 Family with Prelingual Progressive Sensorineural Hearing Impairment. e70134

PloS one, 2013-07, Vol.8 (7)

2013

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Comparative study on the clinical features of familial clustered and sporadic vestibular migraine

Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery, 2021-06, Vol.35 (6), p.525

2021

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Analysis of clinical features of vestibular migraine

Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery, 2020-08, Vol.34 (8), p.726

2020

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Diagnosis, treatment and medical evaluation of head and neck tumors in aircrew

Lin chuang er bi yan hou ke za zhi, 2011-03, Vol.25 (5), p.223

2011

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Preliminary study on diplopore puncture of tympanum and intratympanic administration for management of acute secretory otitis media

Lin chuang er bi yan hou ke za zhi, 2010-01, Vol.24 (1), p.16

2010

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Diagnosis, treatment and medical evaluation of sinusitis and nasal polyp in aircrew

Lin chuang er bi yan hou ke za zhi, 2009-03, Vol.23 (5), p.194

2009

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Characteristics of audiology and clinical genetics of a Chinese family with the DFNA5 genetic hearing loss

Lin chuang er bi yan hou ke za zhi, 2011-05, Vol.25 (9), p.395

2011

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Carotid imaging changes and serum IL-1β, sICAM-1, and sVAP-1 levels in benign paroxysmal positional vertigo

Author Correction: Carotid imaging changes and serum IL-1β, sICAM-1, and sVAP-1 levels in benign paroxysmal positional vertigo

The effect of vascular risk factors on the efficacy of endolymphatic sac decompression surgery for Meniere's disease: a retrospective cohort study

Resolving the genetic heterogeneity of prelingual hearing loss within one family: Performance comparison and application of two targeted next generation sequencing approaches

Loss-of-Function Mutations in the PRPS1 Gene Cause a Type of Nonsyndromic X-linked Sensorineural Deafness, DFN2

Preimplantation genetic diagnosis for a Chinese family with autosomal recessive Meckel-Gruber syndrome type 3 (MKS3)

Identification of a Novel TECTA mutation in a Chinese DFNA8/12 family with prelingual progressive sensorineural hearing impairment

Novel missense mutations in MYO7A underlying postlingual high- or low-frequency non-syndromic hearing impairment in two large families from China

Development and validation of prediction model to estimate vertigo risk after endolymphatic sac decompression in Meniere’s disease: a retrospective cohort study

Qualification of Pilots with Aero-Otitis Media After Balloon Eustachian Tuboplasty

Pilots' Spatial Visualization Ability Assessment Based on Virtual Reality

Dynamic Rabbit Model of Ear Barotrauma

Identification of a novel DFNA5 mutation, IVS7-2 a > G, in a Chinese family with non-syndromic sensorineural hearing loss

A Dynamic Rabbit Model of Sinus Barotrauma and Its Related Pathology

Predictive accuracy of machine learning for radiation-induced temporal lobe injury in nasopharyngeal carcinoma patients: a systematic review and meta-analysis

Identification of two novel missense WFS1 mutations, H696Y and R703H, in patients with non-syndromic low-frequency sensorineural hearing loss

Novel missense mutations in MYO7A underlying postlingual high- or low-frequency non-syndromic hearing impairment in two large families from China

Preimplantation Genetic Diagnosis for a Chinese Family with Autosomal Recessive Meckel-Gruber Syndrome Type 3 (MKS3): e73245

Identification of a Novel TECTA Mutation in a Chinese DFNA8/12 Family with Prelingual Progressive Sensorineural Hearing Impairment. e70134

Comparative study on the clinical features of familial clustered and sporadic vestibular migraine

Analysis of clinical features of vestibular migraine

Diagnosis, treatment and medical evaluation of head and neck tumors in aircrew

Preliminary study on diplopore puncture of tympanum and intratympanic administration for management of acute secretory otitis media

Diagnosis, treatment and medical evaluation of sinusitis and nasal polyp in aircrew

Characteristics of audiology and clinical genetics of a Chinese family with the DFNA5 genetic hearing loss

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