Search Results - "Akita, Jiro"

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  1. 1

    Clinical and genetic features of nonsyndromic autosomal dominant sensorineural hearing loss: KCNQ4 is a gene responsible in Japanese by Akita, J, Abe, S, Shinkawa, H, Kimberling, W J, Usami, S

    Published in Journal of human genetics (01-01-2001)
    “…Sixteen Japanese nonsyndromic autosomal dominant sensorineural hearing loss (ADSNHL) families were investigated clinically as well as genetically. Most…”
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    Journal Article
  2. 2
  3. 3

    Prevalence of mitochondrial gene mutations among hearing impaired patients by Usami, Shin-ichi, Abe, Satoko, Akita, Jiro, Namba, Atsushi, Shinkawa, Hideichi, Ishii, Masanori, Iwasaki, Satoshi, Hoshino, Tomoyuki, Ito, Juichi, Doi, Katsumi, Kubo, Takeshi, Nakagawa, Takashi, Komiyama, Sohtaro, Tono, Tetsuya, Komune, Shizuo

    Published in Journal of medical genetics (01-01-2000)
    “…The frequency of three mitochondrial point mutations, 1555A→G, 3243A→G, and 7445A→G, known to be associated with hearing impairment, was examined using…”
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    Journal Article
  4. 4

    Various Changes of Peripheral Positional Nystagmus by Ichijo, Hiroaki, Akita, Jiro, Ishii, Kenji, Miyakoshi, Yasuharu, Shinkawa, Hideichi

    Published in Equilibrium Research (1996)
    “…Using an infrared CCD camera and electronystagmography, we observed positional nystagmus in 36 patients with peripheral positional vertigo. Patients were…”
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    Journal Article
  5. 5

    Follow-up study of vestibular neuronitis by Ichijo, H, Akita, J, Ishii, K, Miyakoshi, Y, Tominaga, T, Shinkawa, H

    Published in Nippon Jibi Inkoka Gakkai Kaiho (01-02-1996)
    “…A follow-up study of 26 patients with vestibular neuronitis is reported. The disease is characterized by an acute attack of severe vertigo with complete loss…”
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    Journal Article
  6. 6

    A mutational hot spot in the KCNQ4 gene responsible for autosomal dominant hearing impairment by Van Camp, Guy, Coucke, Paul J., Akita, Jiro, Fransen, Erik, Abe, Satoko, De Leenheer, Els M.R., Huygen, Patrick L.M., Cremers, Cor W.R.J., Usami, Shin-Ichi

    Published in Human mutation (01-07-2002)
    “…Several different mutations in the KCNQ4 K+ channel gene are responsible for autosomal dominant nonsyndromic hearing impairment (DFNA2). Here we describe two…”
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    Journal Article
  7. 7

    Five essays on the theory of prudence and precautionary saving by Akita, Jiro

    “…This dissertation consists of five essays on the effect of prudence and risk aversion on optimal saving or investment. Despite the intuitive appeal, the task…”
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    Dissertation
  8. 8

    Five essays on the theory of prudence and precautionary saving by Akita, Jiro

    Published 01-01-1997
    “…This dissertation consists of five essays on the effect of prudence and risk aversion on optimal saving or investment. Despite the intuitive appeal, the task…”
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    Dissertation
  9. 9

    Molecular diagnosis of deafness: impact of gene identification by Usami, Shin-ichi, Koda, Eiko, Tsukamoto, Koji, Otsuka, Akihiro, Yuge, Isamu, Asamura, Kenji, Abe, Satoko, Akita, Jiro, Namba, Atsushi

    Published in Audiology & neurotology (01-05-2002)
    “…Recent progress in identifying genes responsible for hearing loss enables the ENT clinician to apply molecular diagnosis by genetic testing. This article…”
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    Journal Article