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Journal Abstract Search

100 related items for PubMed ID: 10359861

  • 21. [Mitochondrial DNA mutations and non-syndromic sensorineural hearing loss].
    Kong W, Wang Q, Zheng X, Cheng H.
    Zhonghua Er Bi Yan Hou Ke Za Zhi; 2002 Oct; 37(5):338-42. PubMed ID: 12772452
    [Abstract] [Full Text] [Related]

  • 22. [Nonsyndromic inherited hearing impairment caused by mtDNA double mutations of A1555G and 961 insC].
    Cao X, Xing GQ, Wei QJ, Bu XK, Wang DY.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Dec; 21(6):629-32. PubMed ID: 15583999
    [Abstract] [Full Text] [Related]

  • 23. Mitochondrial A7445G mutation in two pedigrees with palmoplantar keratoderma and deafness.
    Sevior KB, Hatamochi A, Stewart IA, Bykhovskaya Y, Allen-Powell DR, Fischel-Ghodsian N, Maw MA.
    Am J Med Genet; 1998 Jan 13; 75(2):179-85. PubMed ID: 9450881
    [Abstract] [Full Text] [Related]

  • 24. Prevalence and clinical features of the mitochondrial m.1555A>G mutation in Taiwanese patients with idiopathic sensorineural hearing loss and association of haplogroup F with low penetrance in three families.
    Wu CC, Chiu YH, Chen PJ, Hsu CJ.
    Ear Hear; 2007 Jun 13; 28(3):332-42. PubMed ID: 17485982
    [Abstract] [Full Text] [Related]

  • 25. Inherited susceptibility to aminoglycoside ototoxicity: genetic heterogeneity and clinical implications.
    Casano RA, Johnson DF, Bykhovskaya Y, Torricelli F, Bigozzi M, Fischel-Ghodsian N.
    Am J Otolaryngol; 1999 Jun 13; 20(3):151-6. PubMed ID: 10326749
    [Abstract] [Full Text] [Related]

  • 26. Aminoglycoside-induced deafness associated with the mitochondrial DNA mutation A1555G.
    Shohat M, Fischel-Ghodsian N, Legum C, Halpern GJ.
    Am J Otolaryngol; 1999 Jun 13; 20(1):64-7. PubMed ID: 9950117
    [No Abstract] [Full Text] [Related]

  • 27. A molecular basis for human hypersensitivity to aminoglycoside antibiotics.
    Hutchin T, Haworth I, Higashi K, Fischel-Ghodsian N, Stoneking M, Saha N, Arnos C, Cortopassi G.
    Nucleic Acids Res; 1993 Sep 11; 21(18):4174-9. PubMed ID: 8414970
    [Abstract] [Full Text] [Related]

  • 28. [Clinical significance of large-scale screening of A1555G mutation of mitochondria DNA for neonates].
    Cai J, Luo CQ, Xie JS, Wu WQ, Geng Q, Xu ZY, Hao Y, Xu XX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Aug 11; 28(4):414-6. PubMed ID: 21811982
    [Abstract] [Full Text] [Related]

  • 29. Genetic aspects of antibiotic induced deafness: mitochondrial inheritance.
    Hu DN, Qui WQ, Wu BT, Fang LZ, Zhou F, Gu YP, Zhang QH, Yan JH, Ding YQ, Wong H.
    J Med Genet; 1991 Feb 11; 28(2):79-83. PubMed ID: 2002491
    [Abstract] [Full Text] [Related]

  • 30. Genetic features, clinical phenotypes, and prevalence of sensorineural hearing loss associated with the 961delT mitochondrial mutation.
    Kobayashi K, Oguchi T, Asamura K, Miyagawa M, Horai S, Abe S, Usami S.
    Auris Nasus Larynx; 2005 Jun 11; 32(2):119-24. PubMed ID: 15917167
    [Abstract] [Full Text] [Related]

  • 31. Myelocystocele-cloacal exstrophy in a pedigree with a mitochondrial 12S rRNA mutation, aminoglycoside-induced deafness, pigmentary disturbances, and spinal anomalies.
    Nye JS, Hayes EA, Amendola M, Vaughn D, Charrow J, McLone DG, Speer MC, Nance WE, Pandya A.
    Teratology; 2000 Mar 11; 61(3):165-71. PubMed ID: 10661905
    [Abstract] [Full Text] [Related]

  • 32. Specific binding of aminoglycosides to a human rRNA construct based on a DNA polymorphism which causes aminoglycoside-induced deafness.
    Hamasaki K, Rando RR.
    Biochemistry; 1997 Oct 07; 36(40):12323-8. PubMed ID: 9315872
    [Abstract] [Full Text] [Related]

  • 33. Pigmentary retinal dystrophy and the syndrome of maternally inherited diabetes and deafness caused by the mitochondrial DNA 3243 tRNA(Leu) A to G mutation.
    Smith PR, Bain SC, Good PA, Hattersley AT, Barnett AH, Gibson JM, Dodson PM.
    Ophthalmology; 1999 Jun 07; 106(6):1101-8. PubMed ID: 10366077
    [Abstract] [Full Text] [Related]

  • 34. Mitochondrial tRNA(Leu(UUR)) gene mutation diabetes mellitus in Chinese.
    Xiang K, Wang Y, Wu S, Lu H, Zheng T, Sun D, Weng Q, Jia W, Shen W, Pu L, He J.
    Chin Med J (Engl); 1997 May 07; 110(5):372-8. PubMed ID: 9594306
    [Abstract] [Full Text] [Related]

  • 35. Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA T1095C mutation in three Chinese families.
    Dai P, Yuan Y, Huang D, Qian Y, Liu X, Han D, Yuan H, Wang X, Young WY, Guan MX.
    Biochem Biophys Res Commun; 2006 Sep 15; 348(1):200-5. PubMed ID: 16875663
    [Abstract] [Full Text] [Related]

  • 36. [Mitochondrial DNA A1555G mutation of seven families with nonsyndromic hearing loss].
    Ou QS, Cheng ZJ, Yang B, Jiang L, Chen J.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Oct 15; 26(5):550-4. PubMed ID: 19806580
    [Abstract] [Full Text] [Related]

  • 37. Different clinical characteristics of aminoglycoside-induced profound deafness with and without the 1555 A-->G mitochondrial mutation.
    Tono T, Kiyomizu K, Matsuda K, Komune S, Usami S, Abe S, Shinkawa H.
    ORL J Otorhinolaryngol Relat Spec; 2001 Oct 15; 63(1):25-30. PubMed ID: 11174059
    [Abstract] [Full Text] [Related]

  • 38. Two large French pedigrees with non syndromic sensorineural deafness and the mitochondrial DNA T7511C mutation: evidence for a modulatory factor.
    Chapiro E, Feldmann D, Denoyelle F, Sternberg D, Jardel C, Eliot MM, Bouccara D, Weil D, Garabédian EN, Couderc R, Petit C, Marlin S.
    Eur J Hum Genet; 2002 Dec 15; 10(12):851-6. PubMed ID: 12461693
    [Abstract] [Full Text] [Related]

  • 39. Prevalence and clinical characteristics of maternally inherited diabetes and deafness caused by the mt3243A > G mutation in young adult diabetic subjects in Sri Lanka.
    Katulanda P, Groves CJ, Barrett A, Sheriff R, Matthews DR, McCarthy MI, Gloyn AL.
    Diabet Med; 2008 Mar 15; 25(3):370-4. PubMed ID: 18279408
    [Abstract] [Full Text] [Related]

  • 40. [The role of mtDNA deletion in the sensitivity to aminoglycoside antibiotic induced deafness].
    Kong W, Liu J, Dong J.
    Zhonghua Er Bi Yan Hou Ke Za Zhi; 2000 Apr 15; 35(2):94-7. PubMed ID: 12768661
    [Abstract] [Full Text] [Related]

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