Kudo T - Search Results

1

A case of basal cell adenocarcinoma of the parotid gland.

Ikeda K, Watanabe M, Oshima T, Nakabayashi S, Kudo T, Sawai T, Takasaka T. Ikeda K, et al. Among authors: kudo t. Tohoku J Exp Med. 1998 Sep;186(1):51-9. doi: 10.1620/tjem.186.51. Tohoku J Exp Med. 1998. PMID: 9915107 Free article.

2

A case of leiomyosarcoma of the sphenoid sinus.

Ikeda K, Kudo T, Shimomura A, Oshima T, Suzuki N, Kakehata S, Nakabayashi S, Yamauchi D, Takasaka T. Ikeda K, et al. Among authors: kudo t. Tohoku J Exp Med. 1997 Jul;182(3):265-70. doi: 10.1620/tjem.182.265. Tohoku J Exp Med. 1997. PMID: 9362110 Free article.

3

Novel mutations in the connexin 26 gene (GJB2) responsible for childhood deafness in the Japanese population.

Kudo T, Ikeda K, Kure S, Matsubara Y, Oshima T, Watanabe Ki, Kawase T, Narisawa K, Takasaka T. Kudo T, et al. Am J Med Genet. 2000 Jan 17;90(2):141-5. doi: 10.1002/(sici)1096-8628(20000117)90:2<141::aid-ajmg10>3.0.co;2-g. Am J Med Genet. 2000. PMID: 10607953

4

Point mutation of the mitochondrial genome in Japanese deaf-mutism.

Oshima T, Kudo T, Ikeda K. Oshima T, et al. Among authors: kudo t. ORL J Otorhinolaryngol Relat Spec. 2001 Nov-Dec;63(6):329-32. doi: 10.1159/000055769. ORL J Otorhinolaryngol Relat Spec. 2001. PMID: 11713420

5

Mutation detection of GJB2 using IsoCode and real-time quantitative polymerase chain reaction with SYBR green I dye for newborn hearing screening.

Kudo T, Oshima T, Kure S, Matsubara Y, Ikeda K. Kudo T, et al. Laryngoscope. 2004 Jul;114(7):1299-304. doi: 10.1097/00005537-200407000-00030. Laryngoscope. 2004. PMID: 15235365

6

GJB2 (connexin 26) mutations and childhood deafness in Thailand.

Kudo T, Ikeda K, Oshima T, Kure S, Tammasaeng M, Prasansuk S, Matsubara Y. Kudo T, et al. Otol Neurotol. 2001 Nov;22(6):858-61. doi: 10.1097/00129492-200111000-00025. Otol Neurotol. 2001. PMID: 11698809

7

Establishment of a new extrahepatic bile duct carcinoma cell line, TFK-1.

Saijyo S, Kudo T, Suzuki M, Katayose Y, Shinoda M, Muto T, Fukuhara K, Suzuki T, Matsuno S. Saijyo S, et al. Among authors: kudo t. Tohoku J Exp Med. 1995 Sep;177(1):61-71. doi: 10.1620/tjem.177.61. Tohoku J Exp Med. 1995. PMID: 8693487 Free article.

8

The effects of hypoxia, premature birth, infection, ototoxic drugs, circulatory system and congenital disease on neonatal hearing loss.

Yoshikawa S, Ikeda K, Kudo T, Kobayashi T. Yoshikawa S, et al. Among authors: kudo t. Auris Nasus Larynx. 2004 Dec;31(4):361-8. doi: 10.1016/j.anl.2004.07.007. Auris Nasus Larynx. 2004. PMID: 15571908

9

A novel KCNQ4 one-base deletion in a large pedigree with hearing loss: implication for the genotype-phenotype correlation.

Kamada F, Kure S, Kudo T, Suzuki Y, Oshima T, Ichinohe A, Kojima K, Niihori T, Kanno J, Narumi Y, Narisawa A, Kato K, Aoki Y, Ikeda K, Kobayashi T, Matsubara Y. Kamada F, et al. Among authors: kudo t. J Hum Genet. 2006;51(5):455-460. doi: 10.1007/s10038-006-0384-7. Epub 2006 Apr 5. J Hum Genet. 2006. PMID: 16596322

10

Outcomes of surgically treated rhinogenic optic neuropathy.

Nakaya K, Oshima T, Kudo T, Ikeda R, Hidaka H, Kobayashi T. Nakaya K, et al. Among authors: kudo t. Acta Otolaryngol. 2011 Aug;131(8):833-9. doi: 10.3109/00016489.2011.557837. Epub 2011 Apr 5. Acta Otolaryngol. 2011. PMID: 21466260

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