Fukushima K - Search Results

1

SOD1 gene polymorphisms in sudden sensorineural hearing loss.

Kitoh R, Nishio SY, Ogawa K, Okamoto M, Kitamura K, Gyo K, Sato H, Nakashima T, Fukuda S, Fukushima K, Hara A, Yamasoba T, Usami S. Kitoh R, et al. Among authors: fukushima k. Acta Otolaryngol. 2016;136(5):465-9. doi: 10.3109/00016489.2015.1116047. Epub 2016 Feb 16. Acta Otolaryngol. 2016. PMID: 26882452

2

Hearing immaturity found by ABR and its clinical impact on otoneurological evaluation.

Kawarai H, Nishizaki K, Fukuda S, Akagi S, Inokuchi I, Gunduz M, Masuda A, Nakashima T, Fukushima K, Masuda Y. Kawarai H, et al. Among authors: fukushima k. Acta Otolaryngol Suppl. 1999;540:6-11. doi: 10.1080/00016489950181116. Acta Otolaryngol Suppl. 1999. PMID: 10445071

3

The alteration of penicillin-binding proteins (PBPs) in drug-resistant Streptococcus pneumoniae isolated from acute otitis media.

Tsurusako Y, Fukushima K, Nishizaki K, Takata T, Ogawa T, Nakashima T, Sugata K, Yorizane S, Ogawara T, Masuda Y. Tsurusako Y, et al. Among authors: fukushima k. Acta Otolaryngol Suppl. 1999;540:67-71. Acta Otolaryngol Suppl. 1999. PMID: 10445083

4

Human papillomavirus as a risk factor for head and neck cancers--a case-control study.

Nishioka S, Fukushima K, Nishizaki K, Gunduz M, Tominaga S, Fukazawa M, Monden N, Watanabe S, Masuda Y, Ogura H. Nishioka S, et al. Among authors: fukushima k. Acta Otolaryngol Suppl. 1999;540:77-80. Acta Otolaryngol Suppl. 1999. PMID: 10445085

5

Sensorineural hearing impairment, non-syndromic: DFNB5, 6, 7. Homozygosity mapping to localize genes causing autosomal recessive non-syndromic hearing loss.

Fukushima K, Ueki Y, Smith RJ. Fukushima K, et al. Adv Otorhinolaryngol. 2000;56:152-7. doi: 10.1159/000059103. Adv Otorhinolaryngol. 2000. PMID: 10868227 Review. No abstract available.

6

DFNB15: autosomal recessive non-syndromic hearing loss gene-chromosome 3q, 19p or digenic recessive inheritance?

Chen AH, Fukushima K, McGuirt WT, Smith RJ. Chen AH, et al. Among authors: fukushima k. Adv Otorhinolaryngol. 2000;56:171-5. doi: 10.1159/000059089. Adv Otorhinolaryngol. 2000. PMID: 10868231 No abstract available.

7

Genetic alteration of penicillin non-susceptible Streptococcus pneumoniae observed throughout recurrence of acute otitis media detected by amplified fragment length polymorphism analysis.

Sugata K, Fukushima K, Ogawa T, Nakashima T, Sugata A, Kasai N, Gunduz M, Ueki Y, Nishizaki K. Sugata K, et al. Among authors: fukushima k. Acta Med Okayama. 2001 Jun;55(3):167-74. doi: 10.18926/AMO/32023. Acta Med Okayama. 2001. PMID: 11434429 Free article.

8

High-throughput screening for GJB2 mutations--its clinical application to genetic testing in prelingual deafness screening for GJB2 mutations.

Sugata A, Fukushima K, Sugata K, Fukuda S, Kimura N, Gunduz M, Kasai N, Usami S, Smith RJ, Nishizaki K. Sugata A, et al. Among authors: fukushima k. Auris Nasus Larynx. 2002 Jul;29(3):231-9. doi: 10.1016/s0385-8146(02)00014-7. Auris Nasus Larynx. 2002. PMID: 12167443

9

Effect of single-drug treatment on idiopathic sudden sensorineural hearing loss.

Kanzaki J, Inoue Y, Ogawa K, Fukuda S, Fukushima K, Gyo K, Yanagihara N, Hoshino T, Ishitoya J, Toriyama M, Kitamura K, Murai K, Nakashima T, Niwa H, Nomura Y, Kobayashi H, Oda M, Okamoto M, Shitara T, Sakagami M, Tono T, Usami S. Kanzaki J, et al. Among authors: fukushima k. Auris Nasus Larynx. 2003 May;30(2):123-7. doi: 10.1016/s0385-8146(03)00009-9. Auris Nasus Larynx. 2003. PMID: 12753981

10

Sudden hearing impairment combined with diabetes mellitus or hyperlipidemia.

Orita S, Fukushima K, Orita Y, Nishizaki K. Orita S, et al. Among authors: fukushima k. Eur Arch Otorhinolaryngol. 2007 Apr;264(4):359-62. doi: 10.1007/s00405-006-0196-6. Epub 2006 Nov 22. Eur Arch Otorhinolaryngol. 2007. PMID: 17119991

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