Hearing impairment in MELAS: new prospective in clinical use of microRNA, a systematic review

被引:0
作者
Arianna Di Stadio
Valentina Pegoraro
Laura Giaretta
Laura Dipietro
Roberta Marozzo
Corrado Angelini
机构
[1] San Camillo Hospital IRCCS,
[2] Highland Instruments,undefined
来源
Orphanet Journal of Rare Diseases | / 13卷
关键词
MELAS; Hearing loss; Hearing impairment; Otoacustic emission; Auditory brain response; microRNA; Diagnosis;
D O I
暂无
中图分类号
学科分类号
摘要
引用
收藏
相关论文
共 186 条
  • [1] Ciafaloni E(1992)MELAS: clinical features, biochemistry, and molecular genetics Ann Neurol 31 391-398
  • [2] Ricci E(2007)Population prevalence of the MELAS A3243G mutation Mitochondrion 7 230-233
  • [3] Shanske S(2001)Progressive sensorineural hearing loss in children with mitochondrial encephalomyopathies Laryngoscope 111 515-521
  • [4] Moraes CT(2016)Both mitochondrial DNA and mitonuclear gene mutations can cause hearing loss through cochlear dysfunction Brain 139 1-5
  • [5] Silvestri G(2016)Reply: Both mitochondrial DNA and mitonuclear gene mutations can cause hearing loss through cochlear dysfunction Brain 140 1-5
  • [6] Hirano M(1993)Pathology in presbycusis Ann Otol Rhinol Laryngol 102 1-16
  • [7] Simonetti S(2012)Histopathologic categorization of presbycusis Otol Neurotol 33 e23-e24
  • [8] Angelini C(2017)MicroRNAs in hearing disorders: their regulation by oxidative stress, inflammation and antioxidants Front Cell Neurosci 11 276-1368
  • [9] Donati MA(2003)Temporal bone histopathological and quantitative analysis of mitochondrial DNA in MELAS Laryngoscope 113 1362-350
  • [10] Garcia C(2010)Quantitative cellular level analysis of mitochondrial DNA 3243A > G mutations in individual tissues from the archival temporal bones of a MELAS patient Acta Otolaryngol 130 344-15