186 related articles for article (PubMed ID: 36182714)
1. Pathogenic mtDNA variants, in particular single large-scale mtDNA deletions, are strongly associated with post-lingual onset sensorineural hearing loss in primary mitochondrial disease.
Elander J; McCormick EM; Värendh M; Stenfeldt K; Ganetzky RD; Goldstein A; Zolkipli-Cunningham Z; MacMullen LE; Xiao R; Falk MJ; Ehinger JK
Mol Genet Metab; 2022 Nov; 137(3):230-238. PubMed ID: 36182714
[TBL] [Abstract][Full Text] [Related]
2. Mitochondrial mutations in maternally inherited hearing loss.
Mutai H; Watabe T; Kosaki K; Ogawa K; Matsunaga T
BMC Med Genet; 2017 Mar; 18(1):32. PubMed ID: 28320335
[TBL] [Abstract][Full Text] [Related]
3. Extended genetic diagnostics for children with profound sensorineural hearing loss by implementing massive parallel sequencing. Diagnostic outcome, family experience and clinical implementation.
Elander J; Ullmark T; Ehrencrona H; Jonson T; Piccinelli P; Samuelsson S; Löwgren K; Falkenius-Schmidt K; Ehinger J; Stenfeldt K; Värendh M
Int J Pediatr Otorhinolaryngol; 2022 Aug; 159():111218. PubMed ID: 35779349
[TBL] [Abstract][Full Text] [Related]
4. Increased risk of hearing loss associated with MT-RNR1 gene mutations: a real-world investigation among Han Taiwanese Population.
Chen HK; Hsieh YW; Hsu HY; Liu TY; Zhang YT; Lin CD; Tsai FJ
BMC Med Genomics; 2024 Jun; 17(1):155. PubMed ID: 38840095
[TBL] [Abstract][Full Text] [Related]
5. Bilateral sensorineural hearing loss associated with the point mutation in mitochondrial genome.
Oshima T; Ueda N; Ikeda K; Abe K; Takasaka T
Laryngoscope; 1996 Jan; 106(1 Pt 1):43-8. PubMed ID: 8544626
[TBL] [Abstract][Full Text] [Related]
6. Prevalence and Clinical Characteristics of Mitochondrial DNA Mutations in Korean Patients With Sensorineural Hearing Loss.
Joo SY; Jang SH; Kim JA; Kim SJ; Kim B; Kim HY; Choi JY; Gee HY; Jung J
J Korean Med Sci; 2023 Dec; 38(48):e355. PubMed ID: 38084023
[TBL] [Abstract][Full Text] [Related]
7. 8-year retrospective analysis of intravenous arginine therapy for acute metabolic strokes in pediatric mitochondrial disease.
Ganetzky RD; Falk MJ
Mol Genet Metab; 2018 Mar; 123(3):301-308. PubMed ID: 29428506
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Etiologic diagnosis of nonsyndromic genetic hearing loss in adult vs pediatric populations.
King PJ; Ouyang X; Du L; Yan D; Angeli SI; Liu XZ
Otolaryngol Head Neck Surg; 2012 Nov; 147(5):932-6. PubMed ID: 22785241
[TBL] [Abstract][Full Text] [Related]
10. The Importance of Mitochondrial Disease Testing in Young Adults With New Onset Sensorineural Hearing Loss.
Koleilat A; Poling GL; Schimmenti LA; Hasadsri L
Ear Hear; 2024 Mar-Apr 01; 45(2):517-521. PubMed ID: 37930162
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Molecular bases of hearing loss in multi-systemic mitochondrial cytopathy.
Scaglia F; Hsu CH; Kwon H; Bai RK; Perng CL; Chang HM; Dai P; Smith EO; Whiteman DA; Feigenbaum A; Gropman A; Wong LJ
Genet Med; 2006 Oct; 8(10):641-52. PubMed ID: 17079881
[TBL] [Abstract][Full Text] [Related]
13. 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]
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. A retrospective cohort study exploring the association between different mitochondrial diseases and hearing loss.
van Kempen CMA; Beynon AJ; Smits JJ; Janssen MCH
Mol Genet Metab; 2022 Apr; 135(4):333-341. PubMed ID: 35190254
[TBL] [Abstract][Full Text] [Related]
16. Sensorineural hearing loss in a pediatric population: association of congenital cytomegalovirus infection with intracranial abnormalities.
Kimani JW; Buchman CA; Booker JK; Huang BY; Castillo M; Powell CM; Weck KE
Arch Otolaryngol Head Neck Surg; 2010 Oct; 136(10):999-1004. PubMed ID: 20956747
[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. Phenotyping mitochondrial DNA-related diseases in childhood: A cohort study of 150 patients.
Ardissone A; Ferrera G; Lamperti C; Tiranti V; Ghezzi D; Moroni I; Lamantea E
Eur J Neurol; 2023 Jul; 30(7):2079-2091. PubMed ID: 37038312
[TBL] [Abstract][Full Text] [Related]
19. Mitochondrial DNA deletion is a predisposing cause for sensorineural hearing loss.
Ueda N; Oshima T; Ikeda K; Abe K; Aoki M; Takasaka T
Laryngoscope; 1998 Apr; 108(4 Pt 1):580-4. PubMed ID: 9546274
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
