Search Results - "namba, Atsushi"

Comprehensive genetic screening of KCNQ4 in a large autosomal dominant nonsyndromic hearing loss cohort: genotype-phenotype correlations and a founder mutation by Naito, Takehiko, Nishio, Shin-ya, Iwasa, Yoh-ichiro, Yano, Takuya, Kumakawa, Kozo, Abe, Satoko, Ishikawa, Kotaro, Kojima, Hiromi, Namba, Atsushi, Oshikawa, Chie, Usami, Shin-ichi

“…The present study of KCNQ4 mutations was carried out to 1) determine the prevalence by unbiased population-based genetic screening, 2) clarify the mutation…”
Get full text

Hearing impairment and cognitive function among a community-dwelling population in Japan by Sugawara, Norio, Sasaki, Akira, Yasui-Furukori, Norio, Kakehata, Seiji, Umeda, Takashi, Namba, Atsushi, Nakaji, Shigeyuki, Shinkawa, Hideichi, Kaneko, Sunao

“…Hearing impairment is a prevalent and chronic condition in older people. This study investigated the relationship between cognitive function and hearing…”
Get full text

Leupeptin, a Calpain Inhibitor, Protects Inner Ear Hair Cells from Aminoglycoside Ototoxicity by Momiyama, Junko, Hashimoto, Toshimitsu, Matsubara, Atsushi, Futai, Kazunori, Namba, Atsushi, Shinkawa, Hideichi

“…Inner ear hair cells play a major role in the auditory pathway that converts sound stimulation into electrical signals, and then into a neural code. However…”
Get full text

Salivary gland carcinoma treated with concomitant chemoradiation with intraarterial cisplatin and docetaxel by Maruya, Shin-ichiro, Namba, Atsushi, Matsubara, Atsushi, Kakehata, Seiji, Takeda, Ikuko, Shirasaki, Takashi, Hatayama, Yoshiomi, Nagahata, Morio, Yokoyama, Junkichi, Shinkawa, Hideichi

“…Malignant neoplasms of the salivary gland are uncommon entities in which surgical resection of the primary lesion has been accepted as a standard therapeutic…”
Get full text

Treatment results of chemotherapy with S-1 for head and neck cancer by Shirasaki, Takashi, Maruya, Shin-ichiro, Namba, Atsushi, Matsubara, Atsushi, Shinkawa, Hideichi

“…A study of chemotherapy treatment with S-1 in patients with head and neck cancer was conducted in 20 patients with residual tumor after primary…”
Get more information

A questionnaire survey of the status of newborn hearing screening in Aomori by Momiyama, Junko, Namba, Atsushi, Abe, Takahisa, Shinkawa, Hideichi

“…Newborn hearing screening (NHS) programs have advanced nationally in Japan, however, differences have been seen in the funding, availability of equipment and…”
Get full text

Hearing investigation in the Iwaki Health Promotional Project by Sakamoto, Natsumi, Sasaki, Akira, Kakehata, Seiji, Futai, Kazunori, Namba, Atsushi, Shinkawa, Hideichi, Takahashi, Ippei, Masashi, Matsuzaka

“…The goal of the Iwaki Health Promotional Project was to prevent illness and promote health in the population of Iwaki town. In our study, a part of this…”
Get full text

Mutation spectrum and genotype-phenotype correlation of hearing loss patients caused by SLC26A4 mutations in the Japanese: a large cohort study by Miyagawa, Maiko, Nishio, Shin-Ya, Usami, Shin-Ichi

“…Mutations in SLC26A4 cause a broad phenotypic spectrum, from typical Pendred syndrome to nonsyndromic hearing loss associated with enlarged vestibular…”
Get full text

A family affected by branchio-oto syndrome with EYA1 mutations by Fukuda, Satoshi, Kuroda, Tsutomu, Chida, Eiji, Shimizu, Rie, Usami, Shin-ichi, Koda, Eiko, Abe, Satoko, Namba, Atsushi, Kitamura, Ken, Inuyama, Yukio

“…Branchio-oto (BO) syndrome is complicated with congenital preauricular fistulae, branchial fistulae (cysts), and hearing loss (sensorineural, conductive or…”
Get full text

Distribution and frequencies of PDS (SLC26A4) mutations in Pendred syndrome and nonsyndromic hearing loss associated with enlarged vestibular aqueduct: a unique spectrum of mutations in Japanese by TSUKAMOTO, Koji, SUZUKI, Hiroaki, HARADA, Daisuke, NAMBA, Atsushi, ABE, Satoko, USAMI, Shin-Ichi

“…Molecular diagnosis makes a substantial contribution to precise diagnosis, subclassification, prognosis, and selection of therapy. Mutations in the PDS…”
Get full text

ASSR検査を用いた労災認定時の詐聴診断 by 南場, 淳司, 阿部, 尚央, 井上, 卓, 武田, 育子, 新川, 秀一

“…労災認定において詐聴, とくに誇大難聴が存在することは広く知られているところである。今回我々は2006年1月から2009年12月までの4年間に当科を受診し騒音性難聴の労災認定を希望した14症例を対象として, 従来施行してきた検査に加えて聴性定常反応検査 (ASSR)…”
Get full text

Immunoelectron microscopic analysis of neurotoxic effect of glutamate in the vestibular end organs during ischemia by Sasaki, Akira, Matsubara, Atsushi, Tabuchi, Keiji, Hara, Akira, Namba, Atsushi, Yamamoto, Youhei, Shinkawa, Hideichi

“…Abstract Conclusion: The excessive glutamate released from the type I and type II hair cells and the supporting cells injure the bouton-type endings and the…”
Get full text

GJB2 deafness gene shows a specific spectrum of mutations in Japan, including a frequent founder mutation by OHTSUKA, Akihiro, YUGE, Isamu, KIMURA, Shinobu, NAMBA, Atsushi, ABE, Satoko, VAN LAER, Lut, VAN CAMP, Guy, USAMI, Shin-Ichi

“…Mutations in the GJB2 gene (connexin 26) are the major cause of autosomal recessive non-syndromic hearing impairment in many populations. In contrast to the…”
Get full text

Frequency of mitochondrial mutations in non-syndromic hearing loss as well as possibly responsible variants found by whole mitochondrial genome screening by Yano, Takuya, Nishio, Shin-ya, Usami, Shin-ichi

“…Mutations in mitochondrial DNA (mtDNA) are reported to be responsible for the pathogenesis of maternally inherited hearing loss. Complete mtDNA sequencing may…”
Get full text

Localization of dopamine receptor subtypes in the rat spiral ganglion by Inoue, Taku, Matsubara, Atsushi, Maruya, Shin-ichiro, Yamamoto, Yohei, Namba, Atsushi, Sasaki, Akira, Shinkawa, Hideichi

“…Although dopaminergic neurons are thought to exist in the lateral olivocochlear efferent system and modulate the afferent nerve activity, the distribution of…”
Get full text

Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of Meniere's disease by Usami, Shin-ichi, Takahashi, Kentaro, Yuge, Isamu, Ohtsuka, Akihiro, Namba, Atsushi, Abe, Satoko, Fransen, Erik, Patthy, Laszlo, Otting, Gottfried, Van Camp, Guy

“…The COCH gene is the only gene identified in man that causes autosomal dominantly inherited hearing loss associated with vestibular dysfunction. The condition…”
Get full text

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

“…The frequency of three mitochondrial point mutations, 1555A→G, 3243A→G, and 7445A→G, known to be associated with hearing impairment, was examined using…”
Get full text

ASSR testing for the detection of exaggerated hearing loss in workers' compensation applications by namba, Atsushi, Abe, Takahisa, Inoue, Taku, Takeda, Ikuko, Shinkawa, Hideichi

“…It is well known that fraudulent applications are sometimes made for workers' compensation disability benefits, and often involve exaggerated claims of hearing…”
Get full text

DC fault analysis of photovoltaic generation system by EMTP by Nagaoka, Naoto, Namba, Atsushi

“…A short-circuit and grounding fault characteristics of a single-phase photovoltaic (PV) generation system are clarified by numerical simulations using…”
Get full text

Comprehensive Genetic Screening of KCNQ4 in a Large Autosomal Dominant Nonsyndromic Hearing Loss Cohort: Genotype-Phenotype Correlations and a Founder Mutation. e63231 by Naito, Takehiko, Nishio, Shin-ya, Iwasa, Yoh-ichiro, Yano, Takuya, Kumakawa, Kozo, Abe, Satoko, Ishikawa, Kotaro, Kojima, Hiromi, Namba, Atsushi, Oshikawa, Chie

“…The present study of KCNQ4 mutations was carried out to 1) determine the prevalence by unbiased population-based genetic screening, 2) clarify the mutation…”
Get full text