These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

126 related articles for article (PubMed ID: 17079881)

  • 61. [Mitochondrial DNA mutations and aminoglycoside antibiotics and hearing loss].
    Qu J; Wang J; Xu S
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2015 Nov; 29(22):1936-40. PubMed ID: 26911053
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Frequency of mitochondrial DNA point mutations among patients with familial sensorineural hearing impairment.
    Lehtonen MS; Uimonen S; Hassinen IE; Majamaa K
    Eur J Hum Genet; 2000 Apr; 8(4):315-8. PubMed ID: 10854117
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Non-Mendelian mitochondrial inheritance as a cause of progressive genetic sensorineural hearing loss.
    Gold M; Rapin I
    Int J Pediatr Otorhinolaryngol; 1994 Aug; 30(2):91-104. PubMed ID: 8063504
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Whole mitochondrial genome screening in maternally inherited non-syndromic hearing impairment using a microarray resequencing mitochondrial DNA chip.
    Lévêque M; Marlin S; Jonard L; Procaccio V; Reynier P; Amati-Bonneau P; Baulande S; Pierron D; Lacombe D; Duriez F; Francannet C; Mom T; Journel H; Catros H; Drouin-Garraud V; Obstoy MF; Dollfus H; Eliot MM; Faivre L; Duvillard C; Couderc R; Garabedian EN; Petit C; Feldmann D; Denoyelle F
    Eur J Hum Genet; 2007 Nov; 15(11):1145-55. PubMed ID: 17637808
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Etiologic diagnosis of sensorineural hearing loss in adults.
    Angeli SI; Yan D; Telischi F; Balkany TJ; Ouyang XM; Du LL; Eshraghi A; Goodwin L; Liu XZ
    Otolaryngol Head Neck Surg; 2005 Jun; 132(6):890-5. PubMed ID: 15944560
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Wild-Type Mitochondrial DNA Copy Number in Urinary Cells as a Useful Marker for Diagnosing Severity of the Mitochondrial Diseases.
    Liu H; Ma Y; Fang F; Zhang Y; Zou L; Yang Y; Zhu S; Wang S; Zheng X; Pei P; Li L; Wu H; Xiao Y; Xu Y; Wang L; Cao Y; Pan H; Qi Y
    PLoS One; 2013; 8(6):e67146. PubMed ID: 23826218
    [TBL] [Abstract][Full Text] [Related]  

  • 67. The mitochondrial A3243G mutation involves the peripheral vestibule as well as the cochlea.
    Iwasaki S; Egami N; Fujimoto C; Chihara Y; Ushio M; Kashio A; Yamasoba T
    Laryngoscope; 2011 Aug; 121(8):1821-4. PubMed ID: 21792976
    [TBL] [Abstract][Full Text] [Related]  

  • 68. The clinical spectrum of maternally transmitted hearing loss.
    Ensink RJ; Huygen PL; Cremers CW
    Adv Otorhinolaryngol; 2002; 61():172-83. PubMed ID: 12408082
    [No Abstract]   [Full Text] [Related]  

  • 69. Nonmuscle Myosin Heavy Chain IIA Mutation Predicts Severity and Progression of Sensorineural Hearing Loss in Patients With MYH9-Related Disease.
    Verver EJ; Topsakal V; Kunst HP; Huygen PL; Heller PG; Pujol-Moix N; Savoia A; Benazzo M; Fierro T; Grolman W; Gresele P; Pecci A
    Ear Hear; 2016; 37(1):112-20. PubMed ID: 26226608
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Multiple origins of the mtDNA 7472insC mutation associated with hearing loss and neurological dysfunction.
    Hutchin TP; Navarro-Coy NC; Van Camp G; Tiranti V; Zeviani M; Schuelke M; Jaksch M; Newton V; Mueller RF
    Eur J Hum Genet; 2001 May; 9(5):385-7. PubMed ID: 11378827
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Hearing evaluation in two sisters with a T8993G point mutation of mitochondrial DNA.
    Sakai Y; Kaga K; Kodama K; Higuchi A; Miyamoto J
    Int J Pediatr Otorhinolaryngol; 2004 Aug; 68(8):1115-9. PubMed ID: 15236904
    [TBL] [Abstract][Full Text] [Related]  

  • 72. A familial case of mitochondrial disease resembling Alport syndrome.
    Fujii H; Mori Y; Kayamori K; Igari T; Ito E; Akashi T; Noguchi Y; Kitamura K; Okado T; Terada Y; Kanda E; Rai T; Uchida S; Sasaki S
    Clin Exp Nephrol; 2008 Apr; 12(2):159-163. PubMed ID: 18180872
    [TBL] [Abstract][Full Text] [Related]  

  • 73. POLG1 p.R722H mutation associated with multiple mtDNA deletions and a neurological phenotype.
    Komulainen T; Hinttala R; Kärppä M; Pajunen L; Finnilä S; Tuominen H; Rantala H; Hassinen I; Majamaa K; Uusimaa J
    BMC Neurol; 2010 May; 10():29. PubMed ID: 20438629
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Early-onset sensorineural hearing loss and late-onset neurologic complaints caused by a mitochondrial mutation at position 7472.
    Ensink RJ; Verhoeven K; Marres HA; Huygen PL; Padberg GW; ter Laak H; van Camp G; Willems PJ; Cremers CW
    Arch Otolaryngol Head Neck Surg; 1998 Aug; 124(8):886-91. PubMed ID: 9708714
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Hearing impairment is common in various phenotypes of the mitochondrial DNA A3243G mutation.
    Deschauer M; Müller T; Wieser T; Schulte-Mattler W; Kornhuber M; Zierz S
    Arch Neurol; 2001 Nov; 58(11):1885-8. PubMed ID: 11708999
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Sudden bilateral hearing loss and sporadic mitochondrial DNA deletion.
    Berrettini S; Forli F; Siciliano G; Mancuso M
    J Laryngol Otol; 2001 Feb; 115(2):128-31. PubMed ID: 11320830
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Audiologic features of hearing loss due to the 1,555 mutation of mitochondrial DNA.
    Tsuiki T; Murai K; Murai S; Kitamura K; Tamagawa Y
    Ann Otol Rhinol Laryngol; 1997 Aug; 106(8):643-8. PubMed ID: 9270426
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Analysis of mitochondrial alterations in Brazilian patients with sensorineural hearing loss using MALDI-TOF mass spectrometry.
    Alves RM; da Silva Costa SM; do Amôr Divino Miranda PM; Ramos PZ; Marconi TG; Santos Oliveira G; Castilho AM; Sartorato EL
    BMC Med Genet; 2016 May; 17(1):41. PubMed ID: 27230773
    [TBL] [Abstract][Full Text] [Related]  

  • 79. Clinical and molecular analysis of a four-generation Chinese family with aminoglycoside-induced and nonsyndromic hearing loss associated with the mitochondrial 12S rRNA C1494T mutation.
    Wang Q; Li QZ; Han D; Zhao Y; Zhao L; Qian Y; Yuan H; Li R; Zhai S; Young WY; Guan MX
    Biochem Biophys Res Commun; 2006 Feb; 340(2):583-8. PubMed ID: 16380089
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Audiologic and genetic features of the A3243G mtDNA mutation.
    Vivero RJ; Ouyang X; Kim YG; Liu W; Du L; Yan D; Liu XZ
    Genet Test Mol Biomarkers; 2013 May; 17(5):383-9. PubMed ID: 23477312
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.