K. Kitamura

发表

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.

Type of mutation in the neurofibromatosis type 2 gene (NF2) frequently determines severity of disease.

R. Weksberg, G. Rouleau, V. Riccardi, 1996, American journal of human genetics.

[Oral allergy syndrome in patients with Japanese cedar pollinosis].

T. Sejima, T. Ishida, K. Murai, 2000, Nihon Jibiinkoka Gakkai kaiho.

Sensorineural hearing impairment non-syndromic, dominant DFNA11.

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

A family affected by branchio-oto syndrome with EYA1 mutations.

S. Fukuda, Y. Inuyama, E. Chida, 2001, Auris, nasus, larynx.

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.

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.

[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.

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

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

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.