Abe S - Search Results

1

Factors that affect hearing level in individuals with the mitochondrial 1555A.G mutation.

Lu SY, Nishio S, Tsukada K, Oguchi T, Kobayashi K, Abe S, Usami S. Lu SY, et al. Among authors: abe s. Clin Genet. 2009 May;75(5):480-4. doi: 10.1111/j.1399-0004.2008.01138.x. Clin Genet. 2009. PMID: 19475720

2

Clinical features of patients with GJB2 (connexin 26) mutations: severity of hearing loss is correlated with genotypes and protein expression patterns.

Oguchi T, Ohtsuka A, Hashimoto S, Oshima A, Abe S, Kobayashi Y, Nagai K, Matsunaga T, Iwasaki S, Nakagawa T, Usami SI. Oguchi T, et al. Among authors: abe s. J Hum Genet. 2005;50(2):76-83. doi: 10.1007/s10038-004-0223-7. Epub 2005 Feb 8. J Hum Genet. 2005. PMID: 15700112

3

Genetic features, clinical phenotypes, and prevalence of sensorineural hearing loss associated with the 961delT mitochondrial mutation.

Kobayashi K, Oguchi T, Asamura K, Miyagawa M, Horai S, Abe S, Usami S. Kobayashi K, et al. Among authors: abe s. Auris Nasus Larynx. 2005 Jun;32(2):119-24. doi: 10.1016/j.anl.2005.01.010. Epub 2005 Mar 24. Auris Nasus Larynx. 2005. PMID: 15917167

4

OTOF mutation screening in Japanese severe to profound recessive hearing loss patients.

Iwasa Y, Nishio SY, Yoshimura H, Kanda Y, Kumakawa K, Abe S, Naito Y, Nagai K, Usami S. Iwasa Y, et al. Among authors: abe s. BMC Med Genet. 2013 Sep 22;14:95. doi: 10.1186/1471-2350-14-95. BMC Med Genet. 2013. PMID: 24053799 Free PMC article.

5

High-frequency involved hearing loss caused by novel mitochondrial DNA mutation in 16S ribosomal RNA gene.

Abe S, Nagano M, Nishio SY, Kumakawa K, Usami S. Abe S, et al. Otol Neurotol. 2014 Jul;35(6):1087-90. doi: 10.1097/MAO.0000000000000350. Otol Neurotol. 2014. PMID: 24770403

6

Sensorineural hearing loss caused by mitochondrial DNA mutations: special reference to the A1555G mutation.

Usami S, Abe S, Shinkawa H, Kimberling WJ. Usami S, et al. Among authors: abe s. J Commun Disord. 1998 Sep-Oct;31(5):423-34; quiz 434-5. doi: 10.1016/s0021-9924(98)00014-8. J Commun Disord. 1998. PMID: 9777488 Review.

7

Phylogenetic analysis of mitochondrial DNA in Japanese pedigrees of sensorineural hearing loss associated with the A1555G mutation.

Abe S, Usami S, Shinkawa H, Weston MD, Overbeck LD, Hoover DM, Kenyon JB, Horai S, Kimberling WJ. Abe S, et al. Eur J Hum Genet. 1998 Nov-Dec;6(6):563-9. doi: 10.1038/sj.ejhg.5200239. Eur J Hum Genet. 1998. PMID: 9887373

8

Rapid mass screening method and counseling for the 1555A-->G mitochondrial mutation.

Usami S, Abe S, Shinkawa H, Inoue Y, Yamaguchi T. Usami S, et al. Among authors: abe s. J Hum Genet. 1999;44(5):304-7. doi: 10.1007/s100380050165. J Hum Genet. 1999. PMID: 10496072

9

Prevalence of mitochondrial gene mutations among hearing impaired patients.

Usami S, Abe S, Akita J, Namba A, Shinkawa H, Ishii M, Iwasaki S, Hoshino T, Ito J, Doi K, Kubo T, Nakagawa T, Komiyama S, Tono T, Komune S. Usami S, et al. Among authors: abe s. J Med Genet. 2000 Jan;37(1):38-40. doi: 10.1136/jmg.37.1.38. J Med Genet. 2000. PMID: 10633132 Free PMC article.

10

Prevalent connexin 26 gene (GJB2) mutations in Japanese.

Abe S, Usami S, Shinkawa H, Kelley PM, Kimberling WJ. Abe S, et al. J Med Genet. 2000 Jan;37(1):41-3. doi: 10.1136/jmg.37.1.41. J Med Genet. 2000. PMID: 10633133 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

4,206 results

Search Page

Filters