126 related articles for article (PubMed ID: 16540924)
1. 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]
2. 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]
3. 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]
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. 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]
6. 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]
7. 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]
8. 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]
9. 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]
10. [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]
11. Prevalence of mitochondrial diabetes in southwestern Finland: a molecular epidemiological study.
Martikainen MH; Rönnemaa T; Majamaa K
Acta Diabetol; 2013 Oct; 50(5):737-41. PubMed ID: 22492248
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. [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]
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. Mitochondrial syndromic sensorineural hearing loss.
Forli F; Passetti S; Mancuso M; Seccia V; Siciliano G; Nesti C; Berrettini S
Biosci Rep; 2007 Jun; 27(1-3):113-23. PubMed ID: 17487579
[TBL] [Abstract][Full Text] [Related]
16. [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]
17. Cochlear alterations in deaf and unaffected subjects carrying the deafness-associated A1555G mutation in the mitochondrial 12S rRNA gene.
Bravo O; Ballana E; Estivill X
Biochem Biophys Res Commun; 2006 Jun; 344(2):511-6. PubMed ID: 16631122
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. [An etiological study in a school for the deaf and radiological findings].
Külahli I; Coşkun A; Ketenci I; Sentürk M; Canöz K
Kulak Burun Bogaz Ihtis Derg; 2006; 16(4):173-7. PubMed ID: 16905909
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]