Found: 9
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Heterozygous SSBP1 start loss mutation co-segregates with hearing loss and the m.1555A>G mtDNA variant in a large multigenerational family.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Both mitochondrial DNA and mitonuclear gene mutations cause hearing loss through cochlear dysfunction.
- Published in:
- 2016
- By:
- Publication type:
- Letter
Current and Emerging Therapies for Chronic Subjective Tinnitus.
- Published in:
- Journal of Clinical Medicine, 2023, v. 12, n. 20, p. 6555, doi. 10.3390/jcm12206555
- By:
- Publication type:
- Article
Cochlear Implantation in Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes Syndrome: Case Presentation.
- Published in:
- 2022
- By:
- Publication type:
- Case Study
Cochlear Implantation Outcomes in Patients with Mitochondrial Hearing Loss: A Systematic Review and Narrative Synthesis.
- Published in:
- Journal of International Advanced Otology, 2021, v. 17, n. 1, p. 72, doi. 10.5152/iao.2020.9226
- By:
- Publication type:
- Article
Impaired Hearing in MELAS.
- Published in:
- Journal of International Advanced Otology, 2022, v. 18, n. 3, p. 276, doi. 10.5152/iao.2022.22750
- By:
- Publication type:
- Article
Otic Langerhans' Cell Histiocytosis in an Adult: A Case Report and Review of the Literature.
- Published in:
- Case Reports in Otolaryngology, 2013, p. 1, doi. 10.1155/2013/259726
- By:
- Publication type:
- Article
Emergency endovascular management of peripheral artery aneurysms and pseudoaneurysms -- a review.
- Published in:
- World Journal of Emergency Surgery, 2008, v. 3, p. 1, doi. 10.1186/1749-7922-3-22
- By:
- Publication type:
- Article
The effect of photobiomodulation on hearing loss: A systematic review.
- Published in:
- Clinical Otolaryngology, 2024, v. 49, n. 1, p. 41, doi. 10.1111/coa.14113
- By:
- Publication type:
- Article