Suzuki H - Search Results

1

Clinical characteristics and genotype-phenotype correlation of hearing loss patients with SLC26A4 mutations.

Suzuki H, Oshima A, Tsukamoto K, Abe S, Kumakawa K, Nagai K, Satoh H, Kanda Y, Iwasaki S, Usami S. Suzuki H, et al. Acta Otolaryngol. 2007 Dec;127(12):1292-7. doi: 10.1080/00016480701258739. Acta Otolaryngol. 2007. PMID: 17851929

2

Distribution and frequencies of PDS (SLC26A4) mutations in Pendred syndrome and nonsyndromic hearing loss associated with enlarged vestibular aqueduct: a unique spectrum of mutations in Japanese.

Tsukamoto K, Suzuki H, Harada D, Namba A, Abe S, Usami S. Tsukamoto K, et al. Among authors: suzuki h. Eur J Hum Genet. 2003 Dec;11(12):916-22. doi: 10.1038/sj.ejhg.5201073. Eur J Hum Genet. 2003. PMID: 14508505

3

The responsible genes in Japanese deafness patients and clinical application using Invader assay.

Usami S, Wagatsuma M, Fukuoka H, Suzuki H, Tsukada K, Nishio S, Takumi Y, Abe S. Usami S, et al. Among authors: suzuki h. Acta Otolaryngol. 2008 Apr;128(4):446-54. doi: 10.1080/00016480701785046. Acta Otolaryngol. 2008. PMID: 18368581 Review.

4

Experience with the Vibrant Soundbridge RW-Coupler for round window Vibroplasty with tympanosclerosis.

Iwasaki S, Suzuki H, Moteki H, Miyagawa M, Takumi Y, Usami S. Iwasaki S, et al. Among authors: suzuki h. Acta Otolaryngol. 2012 Jun;132(6):676-82. doi: 10.3109/00016489.2011.649492. Epub 2012 Mar 4. Acta Otolaryngol. 2012. PMID: 22385350 Free PMC article.

5

Distribution and frequencies of CDH23 mutations in Japanese patients with non-syndromic hearing loss.

Wagatsuma M, Kitoh R, Suzuki H, Fukuoka H, Takumi Y, Usami S. Wagatsuma M, et al. Among authors: suzuki h. Clin Genet. 2007 Oct;72(4):339-44. doi: 10.1111/j.1399-0004.2007.00833.x. Clin Genet. 2007. PMID: 17850630

6

Hybrid carcinoma of the parotid gland: report of a case (epithelial-myoepithelial carcinoma and salivary duct carcinoma) and review of the literature.

Kainuma K, Oshima A, Suzuki H, Fukushima M, Shimojo H, Usami S. Kainuma K, et al. Among authors: suzuki h. Acta Otolaryngol. 2010;130(1):185-9. doi: 10.3109/00016480902930458. Acta Otolaryngol. 2010. PMID: 19449226 Review.

7

A new autosomal recessive form of Stickler syndrome is caused by a mutation in the COL9A1 gene.

Van Camp G, Snoeckx RL, Hilgert N, van den Ende J, Fukuoka H, Wagatsuma M, Suzuki H, Smets RM, Vanhoenacker F, Declau F, Van de Heyning P, Usami S. Van Camp G, et al. Among authors: suzuki h. Am J Hum Genet. 2006 Sep;79(3):449-57. doi: 10.1086/506478. Epub 2006 Jun 26. Am J Hum Genet. 2006. PMID: 16909383 Free PMC article.

8

Preoperative Arterial Embolization to Avoid Intraoperative Bleeding during Endoscopic Sinus Surgery for Organized Hematoma of the Maxillary Sinus: A Case Series and Literature Review.

Kurozumi M, Takumi Y, Uehara T, Suzuki T, Ohya A, Shinagawa J, Miyagawa J, Tsukahara Y, Yamada A, Tsukada K, Suzuki H, Fujinaga Y. Kurozumi M, et al. Among authors: suzuki h, suzuki t. Interv Radiol (Higashimatsuyama). 2021 Nov 1;6(3):102-107. doi: 10.22575/interventionalradiology.2021-0010. eCollection 2021 Nov 1. Interv Radiol (Higashimatsuyama). 2021. PMID: 35912279 Free PMC article.

9

Pseudogap in electron-doped cuprates: Strong correlation leading to band splitting.

Horio M, Sakai S, Suzuki H, Nonaka Y, Hashimoto M, Lu D, Shen ZX, Ohgi T, Konno T, Adachi T, Koike Y, Imada M, Fujimori A. Horio M, et al. Among authors: suzuki h. Proc Natl Acad Sci U S A. 2025 Jan 7;122(1):e2406624122. doi: 10.1073/pnas.2406624122. Epub 2024 Dec 30. Proc Natl Acad Sci U S A. 2025. PMID: 39793056

10

Health Literacy and Internet Use Among Japanese Older Adults: A Gender-Stratified Cross-Sectional Analysis of the Moderating Effects of Neighborhood Relationships.

Nakada T, Kurotani K, Seino S, Kozawa T, Murota S, Eto M, Shimasawa J, Shimizu Y, Tsurugano S, Katsukawa F, Sakamoto K, Washizaki H, Ishigaki Y, Sakamoto M, Takadama K, Yanai K, Matsuo O, Kameue C, Suzuki H, Ohkawara K. Nakada T, et al. Among authors: suzuki h. Healthcare (Basel). 2024 Dec 31;13(1):56. doi: 10.3390/healthcare13010056. Healthcare (Basel). 2024. PMID: 39791663

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