thymine has been researched along with Hearing Loss, Sensorineural in 3 studies
Hearing Loss, Sensorineural: Hearing loss resulting from damage to the COCHLEA and the sensorineural elements which lie internally beyond the oval and round windows. These elements include the AUDITORY NERVE and its connections in the BRAINSTEM.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Lehtonen, MS | 1 |
| Moilanen, JS | 1 |
| Majamaa, K | 1 |
| Leshinsky-Silver, E | 1 |
| Berman, Z | 1 |
| Vinkler, C | 1 |
| Yannov-Sharav, M | 1 |
| Lev, D | 1 |
| Kobayashi, K | 1 |
| Oguchi, T | 1 |
| Asamura, K | 1 |
| Miyagawa, M | 1 |
| Horai, S | 1 |
| Abe, S | 1 |
| Usami, S | 1 |
3 other studies available for thymine and Hearing Loss, Sensorineural
| Article | Year |
|---|---|
Increased variation in mtDNA in patients with familial sensorineural hearing impairment.
Topics: Adenine; Adult; Case-Control Studies; Cytosine; DNA, Mitochondrial; Europe; Female; Finland; Genetic | 2003 |
A novel missense mutation in the Connexin 26 gene associated with autosomal recessive sensorineural deafness.
Topics: Alleles; Base Sequence; Child; Connexin 26; Connexins; Conserved Sequence; Cytosine; Female; Genes, | 2005 |
Genetic features, clinical phenotypes, and prevalence of sensorineural hearing loss associated with the 961delT mitochondrial mutation.
Topics: Adolescent; Adult; Aged; Aminoglycosides; Case-Control Studies; Child; Child, Preschool; DNA, Mitoch | 2005 |