Kitamura K - Search Results

1

Comparison of acute low-tone sensorineural hearing loss versus Meniere's disease by electrocochleography.

Noguchi Y, Nishida H, Tokano H, Kawashima Y, Kitamura K. Noguchi Y, et al. Among authors: kitamura k. Ann Otol Rhinol Laryngol. 2004 Mar;113(3 Pt 1):194-9. doi: 10.1177/000348940411300304. Ann Otol Rhinol Laryngol. 2004. PMID: 15053200

2

Vestibular evoked myogenic potentials in patients with the mitochondrial A1555G mutation.

Kawashima Y, Noguchi Y, Ito T, Kitamura K. Kawashima Y, et al. Among authors: kitamura k. Laryngoscope. 2009 Sep;119(9):1874-9. doi: 10.1002/lary.20584. Laryngoscope. 2009. PMID: 19536740

3

Secondary hyperbaric oxygen therapy for idiopathic sudden sensorineural hearing loss in the subacute and chronic phases.

Ohno K, Noguchi Y, Kawashima Y, Yagishita K, Kitamura K. Ohno K, et al. Among authors: kitamura k. J Med Dent Sci. 2010 Jun;57(2):127-32. J Med Dent Sci. 2010. PMID: 21073130 Clinical Trial.

4

Delayed restoration of maximum speech discrimination scores in patients with idiopathic sudden sensorineural hearing loss.

Noguchi Y, Takahashi M, Ito T, Fujikawa T, Kawashima Y, Kitamura K. Noguchi Y, et al. Among authors: kitamura k. Auris Nasus Larynx. 2016 Oct;43(5):495-500. doi: 10.1016/j.anl.2015.12.003. Epub 2015 Dec 29. Auris Nasus Larynx. 2016. PMID: 26739945

5

Audiological findings in patients with myoclonic epilepsy associated with ragged-red fibres.

Tsutsumi T, Nishida H, Noguchi Y, Komatsuzaki A, Kitamura K. Tsutsumi T, et al. Among authors: kitamura k. J Laryngol Otol. 2001 Oct;115(10):777-81. doi: 10.1258/0022215011909224. J Laryngol Otol. 2001. PMID: 11667986

6

Audiovestibular findings in patients with mitochondrial A1555G mutation.

Noguchi Y, Yashima T, Ito T, Sumi T, Tsuzuku T, Kitamura K. Noguchi Y, et al. Among authors: kitamura k. Laryngoscope. 2004 Feb;114(2):344-8. doi: 10.1097/00005537-200402000-00031. Laryngoscope. 2004. PMID: 14755216

7

[Investigation of automated infant auditory screening using the Natus-ALGO Portable device].

Kawashima Y, Shibahara I, Abe S, Tokano H, Noguchi Y, Kitamura K. Kawashima Y, et al. Among authors: kitamura k. Nihon Jibiinkoka Gakkai Kaiho. 2004 May;107(5):483-8. doi: 10.3950/jibiinkoka.107.483. Nihon Jibiinkoka Gakkai Kaiho. 2004. PMID: 15198008 Japanese.

8

Epidemiological study of mumps deafness in Japan.

Kawashima Y, Ihara K, Nakamura M, Nakashima T, Fukuda S, Kitamura K. Kawashima Y, et al. Among authors: kitamura k. Auris Nasus Larynx. 2005 Jun;32(2):125-8. doi: 10.1016/j.anl.2005.01.009. Epub 2005 Apr 7. Auris Nasus Larynx. 2005. PMID: 15917168

9

A mutation in Wolfram syndrome type 1 gene in a Japanese family with autosomal dominant low-frequency sensorineural hearing loss.

Noguchi Y, Yashima T, Hatanaka A, Uzawa M, Yasunami M, Kimura A, Kitamura K. Noguchi Y, et al. Among authors: kitamura k. Acta Otolaryngol. 2005 Nov;125(11):1189-94. doi: 10.1080/00016480510044232. Acta Otolaryngol. 2005. PMID: 16353398

10

Additional heterozygous 2507A>C mutation of WFS1 in progressive hearing loss at lower frequencies.

Fujikawa T, Noguchi Y, Ito T, Takahashi M, Kitamura K. Fujikawa T, et al. Among authors: kitamura k. Laryngoscope. 2010 Jan;120(1):166-71. doi: 10.1002/lary.20691. Laryngoscope. 2010. PMID: 19877185

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

3,479 results

Search Page

Filters