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Sato M, Ogawa K, Saito H, Yamashita D, Yuge I, Masuda M, Okamoto Y, Kurita A.
[Evaluation of the quality of life in sudden deafness patients by HHIA (hearing Hatidicap Inventory) and questionnaire]
Nippon Jibiinkoka Gakkai Kaiho. 2005 Dec;108(12):1158-64. Japanese.

Yuge I, Takumi Y, Koyabu K, Hashimoto S, Takashima S, Fukuyama T, Nikaido T, Usami S.
Transplanted human amniotic epithelial cells express connexin 26 and Na-K-adenosine triphosphatase in the inner ear.
Transplantation. 2004 May 15;77(9):1452-4.

Usami S, Takahashi K, Yuge I, Ohtsuka A, Namba A, Abe S, Fransen E, Patthy L, Otting G, Van Camp G.
Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of Meniere's disease.
Eur J Hum Genet. 2003 Oct;11(10):744-8.

Imanishi Y, Nameki H, Isobe K, Kaneda T, Yamashita D, Yuge I, Okada W, Nameki I, Araki Y, Suzuki T.
Intramucosal PCO2 measurement as a new monitoring method of free jejunal transfer following pharyngo-laryngo-esophagectomy.
Plast Reconstr Surg. 2003 Oct;112(5):1247-56.

Ohtsuka A, Yuge I, Kimura S, Namba A, Abe S, Van Laer L, Van Camp G, Usami S.
GJB2 deafness gene shows a specific spectrum of mutations in Japan, including a frequent founder mutation.
Hum Genet. 2003 Apr;112(4):329-33. Epub 2003 Jan 31.

Yuge I, Ohtsuka A, Matsunaga T, Usami S.
Identification of 605ins46, a novel GJB2 mutation in a Japanese family.
Auris Nasus Larynx. 2002 Oct;29(4):379-82.

Usami S, Koda E, Tsukamoto K, Otsuka A, Yuge I, Asamura K, Abe S, Akita J, Namba A.
Molecular diagnosis of deafness: impact of gene identification.
Audiol Neurootol. 2002 May-Jun;7(3):185-90.




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