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Human papillomavirus infection among head and neck squamous cell carcinomas in southern China

PloS one, 2019-09, Vol.14 (9), p.e0221045-e0221045

2019

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Intranasal fluticasone furoate in pediatric allergic rhinitis: randomized controlled study

Pediatric research, 2021-05, Vol.89 (7), p.1832-1839

2021

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Diagnostic Errors in Initial Misdiagnosis of Foreign Body Aspiration in Children: A Retrospective Observational Study in a Tertiary Care Hospital in China

Frontiers in pediatrics, 2021-10, Vol.9, p.694211-694211

2021

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Efficacy and Safety of Sublingual Immunotherapy for Allergic Rhinitis in Pediatric Patients: A Meta-Analysis of Randomized Controlled Trials

American journal of rhinology & allergy, 2017-01, Vol.31 (1), p.27-35

2017

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Genetic Polymorphisms and Susceptibility to Sudden Sensorineural Hearing Loss: A Systematic Review

Audiology & neurotology, 2019-01, Vol.24 (1), p.8-19

2019

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Risk factors analysis of attention deficit/hyperactivity disorder and allergic rhinitis in children: a cross-sectional study

Italian journal of pediatrics, 2019-08, Vol.45 (1), p.99-7, Article 99

2019

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Efficacy of Sublingual Immunotherapy for House Dust Mite-Induced Allergic Rhinitis: A Meta-Analysis of Randomized Controlled Trials

Allergy, 2017, Asthma & Immunology Research, 9(3), , pp.220-228

2017

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Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation

Mitochondrion, 2010-01, Vol.10 (1), p.69-81

2010

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Frequency and spectrum of mitochondrial 12S rRNA variants in 440 Han Chinese hearing impaired pediatric subjects from two otology clinics

Journal of translational medicine, 2011-01, Vol.9 (1), p.4-4, Article 4

2011

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Investigation of the prognostic role of neutrophil-to-lymphocyte ratio in Idiopathic Sudden Sensorineural Hearing Loss based on propensity score matching: a retrospective observational study

European archives of oto-rhino-laryngology, 2020-07, Vol.277 (7), p.2107-2113

2020

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Function study of non-syndromic deafness associated mitochondrial 12S rRNA A839G mutation

Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery, 2014-11, Vol.49 (11), p.908

2014

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Prognostic role of haematological indices in sudden sensorineural hearing loss: Review and meta-analysis

Clinica chimica acta, 2018-08, Vol.483, p.104-111

2018

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Efficacy of Sublingual Immunotherapy for House Dust Mite-Induced Allergic Rhinitis: A Meta-Analysis of Randomized Controlled Trials

Allergy, asthma & immunology research, 2022-03, p.220-228

2022

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Association of Pediatric Allergic Rhinitis with the Ratings of Attention-Deficit/Hyperactivity Disorder

American journal of rhinology & allergy, 2017-05, Vol.31 (3), p.161-167

2017

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Clinical Analysis of Sphenoid Sinus Mucocele With Initial Neurological Symptoms

Headache, 2019-09, Vol.59 (8), p.1270-1278

2019

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Mitochondrial tRNAThr G15927A mutation may modulate the phenotypic manifestation of ototoxic 12S rRNA A1555G mutation in four Chinese families

Pharmacogenetics and genomics, 2008-12, Vol.18 (12), p.1059-1070

2008

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Mitochondrial 12S rRNA variants in 1642 Han Chinese pediatric subjects with aminoglycoside-induced and nonsyndromic hearing loss

Mitochondrion, 2010-06, Vol.10 (4), p.380-390

2010

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Mitochondrial tRNA^Glu A14693G variant may modulate the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in a Han Chinese family

Journal of genetics and genomics, 2009-04, Vol.36 (4), p.241-250

2009

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A Deafness- and Diabetes-associated tRNA Mutation Causes Deficient Pseudouridinylation at Position 55 in tRNAGlu and Mitochondrial Dysfunction

The Journal of biological chemistry, 2016-09, Vol.291 (40), p.21029-21041

2016

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A Deafness- and Diabetes-associated tRNA Mutation Causes Deficient Pseudouridinylation at Position 55 in tRNA Glu and Mitochondrial Dysfunction

The Journal of biological chemistry, 2016-09, Vol.291 (40), p.21029-21041

2016

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Mitochondrial ND5 T12338C, tRNACys T5802C, and tRNAThr G15927A variants may have a modifying role in the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese pedigrees

American journal of medical genetics. Part A, 2008-05, Vol.146A (10), p.1248-1258

2008

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Chinese guideline for the diagnosis and treatment of childhood obstructive sleep apnea (2020)

Pediatric investigation, 2021-09, Vol.5 (3), p.167-187

2021

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GSTM1 null genotype is a risk factor for laryngeal cancer

International journal of clinical and experimental medicine, 2015-01, Vol.8 (5), p.7661-7666

2015

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Mitochondrial ND5 T12338C, tRNA(Cys) T5802C, and tRNA(Thr) G15927A variants may have a modifying role in the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese pedigrees

American journal of medical genetics. Part A, 2008-05, Vol.146A (10), p.1248

2008

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Mitochondrial tRNA(Glu) A14693G variant may modulate the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in a Han Chinese family

Journal of genetics and genomics, 2009-04, Vol.36 (4), p.241-250

2009

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Human papillomavirus infection among head and neck squamous cell carcinomas in southern China

Intranasal fluticasone furoate in pediatric allergic rhinitis: randomized controlled study

Diagnostic Errors in Initial Misdiagnosis of Foreign Body Aspiration in Children: A Retrospective Observational Study in a Tertiary Care Hospital in China

Efficacy and Safety of Sublingual Immunotherapy for Allergic Rhinitis in Pediatric Patients: A Meta-Analysis of Randomized Controlled Trials

Genetic Polymorphisms and Susceptibility to Sudden Sensorineural Hearing Loss: A Systematic Review

Risk factors analysis of attention deficit/hyperactivity disorder and allergic rhinitis in children: a cross-sectional study

Efficacy of Sublingual Immunotherapy for House Dust Mite-Induced Allergic Rhinitis: A Meta-Analysis of Randomized Controlled Trials

Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation

Frequency and spectrum of mitochondrial 12S rRNA variants in 440 Han Chinese hearing impaired pediatric subjects from two otology clinics

Investigation of the prognostic role of neutrophil-to-lymphocyte ratio in Idiopathic Sudden Sensorineural Hearing Loss based on propensity score matching: a retrospective observational study

Function study of non-syndromic deafness associated mitochondrial 12S rRNA A839G mutation

Prognostic role of haematological indices in sudden sensorineural hearing loss: Review and meta-analysis

Efficacy of Sublingual Immunotherapy for House Dust Mite-Induced Allergic Rhinitis: A Meta-Analysis of Randomized Controlled Trials

Association of Pediatric Allergic Rhinitis with the Ratings of Attention-Deficit/Hyperactivity Disorder

Clinical Analysis of Sphenoid Sinus Mucocele With Initial Neurological Symptoms

Mitochondrial tRNAThr G15927A mutation may modulate the phenotypic manifestation of ototoxic 12S rRNA A1555G mutation in four Chinese families

Mitochondrial 12S rRNA variants in 1642 Han Chinese pediatric subjects with aminoglycoside-induced and nonsyndromic hearing loss

Mitochondrial tRNA^Glu A14693G variant may modulate the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in a Han Chinese family

A Deafness- and Diabetes-associated tRNA Mutation Causes Deficient Pseudouridinylation at Position 55 in tRNAGlu and Mitochondrial Dysfunction

A Deafness- and Diabetes-associated tRNA Mutation Causes Deficient Pseudouridinylation at Position 55 in tRNA Glu and Mitochondrial Dysfunction

Mitochondrial ND5 T12338C, tRNACys T5802C, and tRNAThr G15927A variants may have a modifying role in the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese pedigrees

Chinese guideline for the diagnosis and treatment of childhood obstructive sleep apnea (2020)

GSTM1 null genotype is a risk factor for laryngeal cancer

Mitochondrial ND5 T12338C, tRNA(Cys) T5802C, and tRNA(Thr) G15927A variants may have a modifying role in the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese pedigrees

Mitochondrial tRNA(Glu) A14693G variant may modulate the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in a Han Chinese family

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