Y. Tamagawa

发表

Mutations of the Pendred syndrome gene (PDS) in patients with large vestibular aqueduct.

Katsumasa Takahashi, K. Kitamura, Y. Noguchi, 2000, Acta oto-laryngologica.

Audiologic Findings in Patients with a Point Mutation at Nucleotide 3,243 of Mitochondrial Dna

M. Nishizawa, T. Ishida, Y. Tamagawa, 1997, The Annals of otology, rhinology, and laryngology.

[Audiologic evaluation in a family showing diabetes mellitus and deafness associated with a mutation in mitochondrial DNA].

T. Ishida, Y. Tamagawa, H. Hagiwara, 1995, Nihon Jibiinkoka Gakkai kaiho.

Phenotype of DFNA11: A Nonsyndromic Hearing Loss Caused by a Myosin VIIA Mutation

T. Tsuru, K. Kitamura, T. Ishida, 2002, The Laryngoscope.

Sensorineural hearing impairment non-syndromic, dominant DFNA11.

K. Steel, M. Nishizawa, T. Ishida, 2000, Advances in oto-rhino-laryngology.

Cytokeratin expression patterns by one- and two-dimensional electrophoresis in pars flaccida cholesteatoma and pars tensa cholesteatoma.

M. Anniko, K. Kitamura, F. Hiraide, 1995, Acta oto-laryngologica.

A new mutation in the POU3F4 gene in a japanese family with x‐linked mixed deafness (DFN3)

Y. Tamagawa, H. Hagiwara, K. Kitamura, 1998, The Laryngoscope.

Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene

Steve D. M. Brown, K. Steel, X. Liu, 1997, Nature Genetics.

Hereditary Sensorineural Hearing Loss of Unknown Cause Involving Mitochondrial DNA 1555 Mutation

S. Iwasaki, S. Ocho, T. Hoshino, 2000, ORL.

Branchial cyst of the nasopharynx: resection via the endonasal approach

M. Miyata, Y. Tamagawa, K. Kitamura, 1995, The Journal of Laryngology & Otology.

Mitochondrial DNA mutation at nucleotide 1555 in a patient with bilateral sensorineural hearing loss of unknown etiology.

K. Abe, M. Nishizawa, T. Ishida, 1996, Acta oto-laryngologica.

A gene for a dominant form of non-syndromic sensorineural deafness (DFNA11) maps within the region containing the DFNB2 recessive deafness gene.

S. Tsuji, M. Nishizawa, Hajime Tanaka, 1996, Human molecular genetics.

Temporal Bone Histopathological and Quantitative Analysis of Mitochondrial DNA in MELAS

S. Merchant, Toshikazu Yamaguchi, Katsumasa Takahashi, 2003, The Laryngoscope.

Molecular genetics in sensorineural hearing loss

K. Kitamura, T. Ishida, Y. Tamagawa, 1996 .

Maternally inherited nonsyndromic hearing loss is associated with the T7511C mutation in the mitochondrial tRNASerUCN gene in a Japanese family.

Selena E. Heman-Ackah, Ronghua Li, Yidong Bai, 2005, Biochemical and biophysical research communications.

Clinical presentation of DFNA11 (MYO7A).

T. Tsuru, K. Kitamura, T. Ishida, 2002, Advances in oto-rhino-laryngology.

[Detection of a mutation in mitochondrial DNA in a family with sensorineural deafness and diabetes mellitus as the predominant clinical features].

M. Nishizawa, T. Ishida, Y. Tamagawa, 1995, Nihon Jibiinkoka Gakkai kaiho.

Nonsyndromic Hearing Loss Caused by a Mitochondrial T7511C Mutation

Katsumasa Takahashi, J. Kusakari, K. Ichimura, 2002, The Laryngoscope.

Temporal Bone Histopathologic Abnormalities Associated With Mitochondrial Mutation T7511C

Katsumasa Takahashi, J. Kusakari, K. Ichimura, 2006, The Laryngoscope.

Audiologic Features of Hearing Loss Due to the 1,555 Mutation of Mitochondrial DNA

T. Tsuiki, K. Murai, Y. Tamagawa, 1997, The Annals of otology, rhinology, and laryngology.