Kitamura K - Search Results

1

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

2

Novel ATP6V1B1 mutations in distal renal tubular acidosis and hearing loss.

Yashima T, Noguchi Y, Kawashima Y, Rai T, Ito T, Kitamura K. Yashima T, et al. Among authors: kitamura k. Acta Otolaryngol. 2010 Sep;130(9):1002-8. doi: 10.3109/00016481003631529. Acta Otolaryngol. 2010. PMID: 20233014

3

Audiovestibular findings in a branchio-oto syndrome patient with a SIX1 mutation.

Noguchi Y, Ito T, Nishio A, Honda K, Kitamura K. Noguchi Y, et al. Among authors: kitamura k. Acta Otolaryngol. 2011 Apr;131(4):413-8. doi: 10.3109/00016489.2010.543146. Epub 2011 Jan 24. Acta Otolaryngol. 2011. PMID: 21254961

4

Mitochondrial DNA haplogroup associated with hereditary hearing loss in a Japanese population.

Kato T, Fuku N, Noguchi Y, Murakami H, Miyachi M, Kimura Y, Tanaka M, Kitamura K. Kato T, et al. Among authors: kitamura k. Acta Otolaryngol. 2012 Nov;132(11):1178-82. doi: 10.3109/00016489.2012.693624. Epub 2012 Jul 25. Acta Otolaryngol. 2012. PMID: 22830575

5

A DFNA5 mutation identified in Japanese families with autosomal dominant hereditary hearing loss.

Nishio A, Noguchi Y, Sato T, Naruse TK, Kimura A, Takagi A, Kitamura K. Nishio A, et al. Among authors: kitamura k. Ann Hum Genet. 2014 Mar;78(2):83-91. doi: 10.1111/ahg.12053. Epub 2014 Feb 10. Ann Hum Genet. 2014. PMID: 24506266

6

Mutation of the EYA1 gene in patients with branchio-oto syndrome.

Yashima T, Noguchi Y, Ishikawa K, Mizusawa H, Kitamura K. Yashima T, et al. Among authors: kitamura k. Acta Otolaryngol. 2003 Jan;123(2):279-82. doi: 10.1080/0036554021000028103. Acta Otolaryngol. 2003. PMID: 12701758

7

Mutations of the Pendred syndrome gene (PDS) in patients with large vestibular aqueduct.

Kitamura K, Takahashi K, Noguchi Y, Kuroishikawa Y, Tamagawa Y, Ishikawa K, Ichimura K, Hagiwara H. Kitamura K, et al. Acta Otolaryngol. 2000 Mar;120(2):137-41. doi: 10.1080/000164800750000775. Acta Otolaryngol. 2000. PMID: 11603758

8

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

9

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

10

SIX1 mutation associated with enlargement of the vestibular aqueduct in a patient with branchio-oto syndrome.

Ito T, Noguchi Y, Yashima T, Kitamura K. Ito T, et al. Among authors: kitamura k. Laryngoscope. 2006 May;116(5):796-9. doi: 10.1097/01.mlg.0000209096.40400.96. Laryngoscope. 2006. PMID: 16652090

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