BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

152 related articles for article (PubMed ID: 16540920)

  • 1. Diabetes, sensorineural deafness, and mitochondrial DNA mutation.
    Prisco F; Iafusco D
    Laryngoscope; 2006 Mar; 116(3):505-6; author reply 506. PubMed ID: 16540920
    [No Abstract]   [Full Text] [Related]  

  • 2. Sensorineural hearing loss, diabetes, and mitochondrial DNA mutation in Taiwan.
    Tseng FY
    Laryngoscope; 2006 Mar; 116(3):506. PubMed ID: 16540924
    [No Abstract]   [Full Text] [Related]  

  • 3. Role of mitochondrial variation in maternally inherited diabetes and deafness syndrome.
    Howes T; Madden C; Dasgupta S; Saeed S; Das V
    J Laryngol Otol; 2008 Nov; 122(11):1249-52. PubMed ID: 18950542
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Frequency and clinical features of patients with sensorineural hearing loss associated with the A3243G mutation of the mitochondrial DNA in otorhinolaryngic clinics.
    Nagata H; Kumahara K; Tomemori T; Arimoto Y; Isoyama K; Yoshida K; Konno A
    J Hum Genet; 2001; 46(10):595-9. PubMed ID: 11587074
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Progressive sensorineural hearing impairment in maternally inherited diabetes mellitus and deafness (MIDD).
    Hendrickx JJ; Mudde AH; 't Hart LM; Huygen PL; Cremers CW
    Otol Neurotol; 2006 Sep; 27(6):802-8. PubMed ID: 16788417
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The frequency in New Zealand of a mitochondrial DNA mutation (1555 A to G) associated with aminoglycoside-induced hearing loss.
    Scrimshaw BJ; Faed JM; Tate WP; Yun K
    N Z Med J; 1999 Jun; 112(1089):216-7. PubMed ID: 10414625
    [No Abstract]   [Full Text] [Related]  

  • 7. [Maternally inherited diabetes and deafness: a case report].
    Maseda E; Sampedro A; Ablanedo A; Alonso JR
    Acta Otorrinolaringol Esp; 2008 Nov; 59(9):472-3. PubMed ID: 19080780
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Importance of searching for mtDNA defects in patients with diabetes and hearing deficit.
    Paquis-Flucklinger V; Vialettes B; Vague P; Canivet B; Hieronimus S; Oliver C; Pellissier JF; Saunières A; Desnuelle C
    Diabetologia; 1998 Jun; 41(6):740-1. PubMed ID: 9662060
    [No Abstract]   [Full Text] [Related]  

  • 9. Genetic predisposition and sensorineural hearing loss following bacterial meningitis: is there a link?
    Jayarajan V; Patton MA; Rajenderkumar D
    J Infect; 2002 Apr; 44(3):210. PubMed ID: 12099760
    [No Abstract]   [Full Text] [Related]  

  • 10. 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; 28(3):332-42. PubMed ID: 17485982
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Analysis of mitochondrial 12S rRNA and tRNA(Ser(UCN)) genes in patients with nonsyndromic sensorineural hearing loss from various regions of Russia].
    Dzhemileva LU; Posukh OL; Tazetdinov AM; Barashkov NA; Zhuravskiĭ SG; Ponidelko SN; Markova TG; Tadinova VN; Fedorova SA; Maksimova NR; Khusnutdinova EK
    Genetika; 2009 Jul; 45(7):982-91. PubMed ID: 19705751
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Dilated cardiomyopathy, diabetes and deafness related to a mutation of mitochondrial DNA].
    Ferreira-Maldent N; Maillot F; Quilliet L; Guilmot JL; Charbonnier B
    Arch Mal Coeur Vaiss; 2007 Feb; 100(2):149-52. PubMed ID: 17474502
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [From gene to disease; mutation in mitochondrial DNA and maternally inherited diabetes mellitus with deafness (MIDD)].
    Leys AM; de Jong PT
    Ned Tijdschr Geneeskd; 2001 Nov; 145(46):2250-2. PubMed ID: 11757250
    [No Abstract]   [Full Text] [Related]  

  • 14. Mitochondrial non-syndromic sensorineural hearing loss: a clinical, audiological and pathological study from Italy, and revision of the literature.
    Berrettini S; Forli F; Passetti S; Rocchi A; Pollina L; Cecchetti D; Mancuso M; Siciliano G
    Biosci Rep; 2008 Feb; 28(1):49-59. PubMed ID: 18215147
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Ototoxicity after use of neomycin eardrops is unrelated to A1555G point mutation in mitochondrial DNA.
    Yamasoba T; Tsukuda K
    J Laryngol Otol; 2004 Jul; 118(7):546-50. PubMed ID: 15318963
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The spectrum of clinical presentation, diagnosis, and management of mitochondrial forms of diabetes.
    Karaa A; Goldstein A
    Pediatr Diabetes; 2015 Feb; 16(1):1-9. PubMed ID: 25330715
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Macular pattern dystrophy associated with a mutation of mitochondrial DNA.
    Massin P; Guillausseau PJ; Vialettes B; Paquis V; Orsini F; Grimaldi AD; Gaudric A
    Am J Ophthalmol; 1995 Aug; 120(2):247-8. PubMed ID: 7639309
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Diabetes mellitus in connection with a hereditary disorder].
    Boomsma LJ
    Ned Tijdschr Geneeskd; 1997 Aug; 141(33):1632. PubMed ID: 9543772
    [No Abstract]   [Full Text] [Related]  

  • 19. A mutation in mitochondrial 12S rRNA, A827G, in Argentinean family with hearing loss after aminoglycoside treatment.
    Chaig MR; Zernotti ME; Soria NW; Romero OF; Romero MF; Gerez NM
    Biochem Biophys Res Commun; 2008 Apr; 368(3):631-6. PubMed ID: 18261986
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A case of diabetes, deafness, cardiomyopathy, and central sleep apnea: novel mitochondrial DNA polymorphisms.
    Sakaue S; Ohmuro J; Mishina T; Miyazaki H; Yamaguchi E; Nishimura M; Fujita M; Nagashima K; Tagami S; Kawakami Y
    Tohoku J Exp Med; 2002 Mar; 196(3):203-11. PubMed ID: 12002277
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.