112 related articles for article (PubMed ID: 12372057)
1. The A1555G mtDNA mutation in Danish hearing-impaired patients: frequency and clinical signs.
ØStergaard E; Montserrat-Sentis B; Grønskov K; Brøndum-Nielsen K
Clin Genet; 2002 Oct; 62(4):303-5. PubMed ID: 12372057
[TBL] [Abstract][Full Text] [Related]
2. [Prevalence of the A1555G MTDNA mutation in sporadic hearing-impaired patients without known history of aminoglycoside treatment].
Morales Angulo C; Gallo-Terán J; Señaris B; Fontalva A; González-Aguado R; Fernández-Luna JL
Acta Otorrinolaringol Esp; 2011; 62(2):83-6. PubMed ID: 21129708
[TBL] [Abstract][Full Text] [Related]
3. Extremely low penetrance of hearing loss in four Chinese families with the mitochondrial 12S rRNA A1555G mutation.
Young WY; Zhao L; Qian Y; Wang Q; Li N; Greinwald JH; Guan MX
Biochem Biophys Res Commun; 2005 Mar; 328(4):1244-51. PubMed ID: 15708009
[TBL] [Abstract][Full Text] [Related]
4. The A1555G mitochondrial DNA mutation in Greek patients with non-syndromic, sensorineural hearing loss.
Kokotas H; Grigoriadou M; Korres GS; Ferekidou E; Papadopoulou E; Neou P; Giannoulia-Karantana A; Kandiloros D; Korres S; Petersen MB
Biochem Biophys Res Commun; 2009 Dec; 390(3):755-7. PubMed ID: 19835846
[TBL] [Abstract][Full Text] [Related]
5. Sensorineural hearing loss caused by mitochondrial DNA mutations: special reference to the A1555G mutation.
Usami S; Abe S; Shinkawa H; Kimberling WJ
J Commun Disord; 1998; 31(5):423-34; quiz 434-5. PubMed ID: 9777488
[TBL] [Abstract][Full Text] [Related]
6. Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment of aminoglycosides.
Estivill X; Govea N; Barceló E; Badenas C; Romero E; Moral L; Scozzri R; D'Urbano L; Zeviani M; Torroni A
Am J Hum Genet; 1998 Jan; 62(1):27-35. PubMed ID: 9490575
[TBL] [Abstract][Full Text] [Related]
7. Mutation A1555G in the 12S rRNA gene and its epidemiological importance in German, Hungarian, and Polish patients.
Kupka S; Tóth T; Wróbel M; Zeissler U; Szyfter W; Szyfter K; Niedzielska G; Bal J; Zenner HP; Sziklai I; Blin N; Pfister M
Hum Mutat; 2002 Mar; 19(3):308-9. PubMed ID: 11857751
[TBL] [Abstract][Full Text] [Related]
8. Cochlear implantation in a patient with profound hearing loss with the A1555G mitochondrial DNA mutation and no history of aminoglycoside exposure.
Ulubil SA; Furze AD; Angeli SI
J Laryngol Otol; 2006 Mar; 120(3):230-2. PubMed ID: 16359140
[TBL] [Abstract][Full Text] [Related]
9. Screening of the mitochondrial A1555G mutation in patients with sensorineural hearing loss.
Maniglia LP; Moreira BCL; da Silva MAOM; Piatto VB; Maniglia JV
Braz J Otorhinolaryngol; 2008; 74(5):731-736. PubMed ID: 19082356
[TBL] [Abstract][Full Text] [Related]
10. A maternal hereditary deafness pedigree of the A1555G mitochondrial mutation, causing aminoglycoside ototoxicity predisposition.
Bai YH; Ren CC; Gong XR; Meng LP
J Laryngol Otol; 2008 Oct; 122(10):1037-41. PubMed ID: 18282333
[TBL] [Abstract][Full Text] [Related]
11. [Audiometric features of familial hearing impairment transmitted by mitochondrial inheritance (A1555G)].
Morales Angulo C; Gallo Terán J; del Castillo I; Moreno Pelayo MA; García-Mantilla J; Moreno Herrero F
Acta Otorrinolaringol Esp; 2002 Nov; 53(9):641-8. PubMed ID: 12584878
[TBL] [Abstract][Full Text] [Related]
12. Study of mitochondrial DNA A1555G and C1494T mutations in a large cohort of women individuals.
Wang L; Wang X; Cai X; Qiang R
Mitochondrial DNA A DNA Mapp Seq Anal; 2019 Mar; 30(2):222-225. PubMed ID: 29790807
[TBL] [Abstract][Full Text] [Related]
13. Audiological and genetic features of the mtDNA mutations.
Liu XZ; Angeli S; Ouyang XM; Liu W; Ke XM; Liu YH; Liu SX; Du LL; Deng XW; Yuan H; Yan D
Acta Otolaryngol; 2008 Jul; 128(7):732-8. PubMed ID: 18568513
[TBL] [Abstract][Full Text] [Related]
14. [Mitochondrial A1555G mutation. Molecular genetic diagnosis in sporadic cases of non-syndromic hearing impairment].
Kupka S; Bodden-Kamps B; Baur M; Zenner HP; Pfister M
HNO; 2004 Nov; 52(11):968-72. PubMed ID: 15309320
[TBL] [Abstract][Full Text] [Related]
15. Investigation of the mtDNA mutations in Syrian families with non-syndromic sensorineural hearing loss.
Moassass F; Al-Halabi B; Nweder MS; Al-Achkar W
Int J Pediatr Otorhinolaryngol; 2018 Oct; 113():110-114. PubMed ID: 30173967
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. Prevalence of the mitochondrial DNA A1555G mutation in sensorineural deafness patients in island Southeast Asia.
Malik SG; Pieter N; Sudoyo H; Kadir A; Marzuki S
J Hum Genet; 2003; 48(9):480-483. PubMed ID: 12955586
[TBL] [Abstract][Full Text] [Related]
19. [Familial susceptibility to aminoglycoside ototoxicity due to the A1555G mutation in the mitochondrial DNA].
Gallo-Terán J; Morales-Angulo C; del Castillo I; Moreno-Pelayo MA; Mazón A; Moreno F
Med Clin (Barc); 2003 Jul; 121(6):216-8. PubMed ID: 12882732
[TBL] [Abstract][Full Text] [Related]
20. [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]
[Next] [New Search]