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1.
Intranasal fluticasone furoate in pediatric allergic rhinitis: randomized controlled study.
Pediatr Res
; 89(7): 1832-1839, 2021 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-33007780
2.
mTOR/NF-κB signaling pathway protects hippocampal neurons from injury induced by intermittent hypoxia in rats.
Int J Neurosci
; 131(10): 994-1003, 2021 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-32378972
3.
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.
Eur Arch Otorhinolaryngol
; 277(7): 2107-2113, 2020 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-32170418
4.
Clinical Analysis of Sphenoid Sinus Mucocele With Initial Neurological Symptoms.
Headache
; 59(8): 1270-1278, 2019 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-31342517
5.
Genetic Polymorphisms and Susceptibility to Sudden Sensorineural Hearing Loss: A Systematic Review.
Audiol Neurootol
; 24(1): 8-19, 2019.
Artículo
en Inglés
| MEDLINE | ID: mdl-30870848
6.
A Deafness- and Diabetes-associated tRNA Mutation Causes Deficient Pseudouridinylation at Position 55 in tRNAGlu and Mitochondrial Dysfunction.
J Biol Chem
; 291(40): 21029-21041, 2016 Sep 30.
Artículo
en Inglés
| MEDLINE | ID: mdl-27519417
7.
[Mitochondrial 12S rRNA A1555G mutation associated with nonsyndromic hearing loss in twenty-five Han Chinese pedigrees].
Yi Chuan
; 35(1): 62-72, 2013 Jan.
Artículo
en Zh
| MEDLINE | ID: mdl-23357266
8.
[Prevalence of common genetic mutations and clinical characteristics analysis in patients at different ages with nonsyndromic hearing impairment].
Yi Chuan
; 35(3): 352-8, 2013 Mar.
Artículo
en Zh
| MEDLINE | ID: mdl-23575541
9.
[Characterization of two Chinese families with aminoglycoside-induced and nonsyndromic hearing loss both carrying a mitochondrial 12S rRNA 1494C>T mutation].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 29(4): 382-7, 2012 Aug.
Artículo
en Zh
| MEDLINE | ID: mdl-22875491
10.
[Spectrum and frequency of mitochondrial 12S rRNA variants in the Chinese subjects with nonsynrdomic hearing loss in Zhejiang Province].
Yi Chuan
; 34(6): 695-704, 2012 Jun.
Artículo
en Zh
| MEDLINE | ID: mdl-22698740
11.
Mutation of SLC7A14 causes auditory neuropathy and retinitis pigmentosa mediated by lysosomal dysfunction.
Sci Adv
; 8(14): eabk0942, 2022 04 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-35394837
12.
Frequency and spectrum of mitochondrial 12S rRNA variants in 440 Han Chinese hearing impaired pediatric subjects from two otology clinics.
J Transl Med
; 9: 4, 2011 Jan 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-21205314
13.
[Maternally inherited aminoglycoside-induced and nonsyndromic hearing loss in five Han Chinese pedigrees].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 28(4): 367-73, 2011 Aug.
Artículo
en Zh
| MEDLINE | ID: mdl-21811972
14.
Diagnostic Errors in Initial Misdiagnosis of Foreign Body Aspiration in Children: A Retrospective Observational Study in a Tertiary Care Hospital in China.
Front Pediatr
; 9: 694211, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-34722414
15.
A cross-sectional survey on occupational stress and associated dyslipidemia among medical staff in tertiary public hospitals in Wenzhou, China.
Brain Behav
; 11(3): e02014, 2021 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-33369267
16.
Predictors of the Prevalence of Dyslipidemia and Influencing Factors for Young Health Examination Cohort: A Cross-Sectional Survey.
Front Public Health
; 8: 400, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-33072681
17.
Risk factors analysis of attention deficit/hyperactivity disorder and allergic rhinitis in children: a cross-sectional study.
Ital J Pediatr
; 45(1): 99, 2019 Aug 13.
Artículo
en Inglés
| MEDLINE | ID: mdl-31409392
18.
Safety and Immunogenicity of a Nonadjuvant Human Papillomavirus Type 6 Virus-like Particle Vaccine in Recurrent Respiratory Papillomatosis.
J Voice
; 33(3): 363-369, 2019 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-30224308
19.
Human papillomavirus infection among head and neck squamous cell carcinomas in southern China.
PLoS One
; 14(9): e0221045, 2019.
Artículo
en Inglés
| MEDLINE | ID: mdl-31545798
20.
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.
Am J Med Genet A
; 146A(10): 1248-58, 2008 May 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-18386806