Iwasaki S - 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. Among authors: iwasaki s. Acta Otolaryngol. 2007 Dec;127(12):1292-7. doi: 10.1080/00016480701258739. Acta Otolaryngol. 2007. PMID: 17851929

2

Association of clinical features with mutation of TECTA in a family with autosomal dominant hearing loss.

Iwasaki S, Harada D, Usami S, Nagura M, Takeshita T, Hoshino T. Iwasaki S, et al. Arch Otolaryngol Head Neck Surg. 2002 Aug;128(8):913-7. doi: 10.1001/archotol.128.8.913. Arch Otolaryngol Head Neck Surg. 2002. PMID: 12162770

3

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: iwasaki 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

4

Association of SLC26A4 mutations with clinical features and thyroid function in deaf infants with enlarged vestibular aqueduct.

Iwasaki S, Tsukamoto K, Usami S, Misawa K, Mizuta K, Mineta H. Iwasaki S, et al. J Hum Genet. 2006;51(9):805-810. doi: 10.1007/s10038-006-0027-z. Epub 2006 Aug 19. J Hum Genet. 2006. PMID: 16924389

5

Achievement of hearing preservation in the presence of an electrode covering the residual hearing region.

Usami S, Moteki H, Suzuki N, Fukuoka H, Miyagawa M, Nishio SY, Takumi Y, Iwasaki S, Jolly C. Usami S, et al. Among authors: iwasaki s. Acta Otolaryngol. 2011 Apr;131(4):405-12. doi: 10.3109/00016489.2010.539266. Epub 2011 Jan 5. Acta Otolaryngol. 2011. PMID: 21208024 Free PMC article.

6

Novel USH2A mutations in Japanese Usher syndrome type 2 patients: marked differences in the mutation spectrum between the Japanese and other populations.

Nakanishi H, Ohtsubo M, Iwasaki S, Hotta Y, Usami S, Mizuta K, Mineta H, Minoshima S. Nakanishi H, et al. Among authors: iwasaki s. J Hum Genet. 2011 Jul;56(7):484-90. doi: 10.1038/jhg.2011.45. Epub 2011 May 19. J Hum Genet. 2011. PMID: 21593743

7

Clinical profile of hearing loss in children with congenital cytomegalovirus (CMV) infection: CMV DNA diagnosis using preserved umbilical cord.

Furutate S, Iwasaki S, Nishio SY, Moteki H, Usami S. Furutate S, et al. Among authors: iwasaki s. Acta Otolaryngol. 2011 Sep;131(9):976-82. doi: 10.3109/00016489.2011.583268. Epub 2011 May 26. Acta Otolaryngol. 2011. PMID: 21612560 Free PMC article.

8

[Multicenter clinical study of bone-anchored hearing aids in Japan--application for congenital auricular atresia].

Fukushima K, Kariya S, Nagayasu R, Fukuda S, Kobayashi T, Kitamura K, Kumakawa K, Usami S, Iwasaki S, Doi K, Gyo K, Tono T, Nishizaki K. Fukushima K, et al. Among authors: iwasaki s. Nihon Jibiinkoka Gakkai Kaiho. 2011 Sep;114(9):761-7. doi: 10.3950/jibiinkoka.114.761. Nihon Jibiinkoka Gakkai Kaiho. 2011. PMID: 22073602 Japanese.

9

Language development in Japanese children who receive cochlear implant and/or hearing aid.

Iwasaki S, Nishio S, Moteki H, Takumi Y, Fukushima K, Kasai N, Usami S. Iwasaki S, et al. Int J Pediatr Otorhinolaryngol. 2012 Mar;76(3):433-8. doi: 10.1016/j.ijporl.2011.12.027. Epub 2012 Jan 26. Int J Pediatr Otorhinolaryngol. 2012. PMID: 22281374 Free article.

10

Simultaneous screening of multiple mutations by invader assay improves molecular diagnosis of hereditary hearing loss: a multicenter study.

Usami S, Nishio SY, Nagano M, Abe S, Yamaguchi T; Deafness Gene Study Consortium. Usami S, et al. PLoS One. 2012;7(2):e31276. doi: 10.1371/journal.pone.0031276. Epub 2012 Feb 24. PLoS One. 2012. PMID: 22384008 Free PMC article.

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