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[Publications] Iwasaki S, Harada D, Usami S, Nagura M, Takeshita T, Hoshino T.: "Association of Clinical Features with Mutation of TECTA in an Autosomal Dominant Hearing Loss Family"Arch Otolaryngol Head Neck Surg 2002. (in press). (2002)
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[Publications] Usami S, Koda E, Tsukamoto K, Otsuka A, Yuge I, Asamura K.: "Molecular diagnosisi of deafness-impact of gene identification"Audiology & Neurootology 2002. (in press). (2002)
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[Publications] Ishinaga H, Shimizu T, Yuta A, Usami S, Tsukamoto K, Majima Y.: "endred's syndrome with goiter and enlarged vestibular aqueducts diagnosed by PDS gene mutation"Head and Neck 2002. (in press). (2002)
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[Publications] Van Camp G, Coucke PJ, Akita J, Fransen E, Abe S.: "Leenheer EMRD, Huygen PLM, Cremers CWRJ, Usami S. A mutational hot spot in the KCNQ4 gene, responsible for autosomal dominant hearing impairment"Human Mutation 2002. (in press). (2002)
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[Publications] Akita J, Abe S, Shinkawa H, Kimberling WJ, Usami S: "Clinical and genetic features of non-syndromic autosomal dominant sensorineural hearing loss : KCNQ4 is a responsible gene in Japanese"J Hum Genet. 46. 355-361 (2001)
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[Publications] Iwasaki S, Usami S, Abe S, Isoda H, Watanabe T, Hoshino T.: "Long-term audiological feature in Pendred syndrome caused by PDS mutation"Arch Otolaryngol Head Neck Surg. 127(6). 705-708 (2001)
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[Publications] Masuda M, Usami S, Yamazaki K, Takumi Y, Shinkawa H, Kurashima K, Kunihiro T, Kanzaki J.: "Connexin 26 distribution in gap junctions between melanocytes in the human vestibular dark cell area"Anat Rec. 262(2). 137-146 (2001)
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[Publications] Takumi Y, Matsubara A, Tsuchida S, Ottersen OP, Shinkawa H, Usami S.: "Takumi Y, Matsubara A, Tsuchida S, Ottersen OP, Shinkawa H, Usami S."Neuroreport. 12(7). 1513-1516 (2001)
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[Publications] Tono T, Kiyomizu K, Matsuda K, Komune S, Usami S, Abe S, Shinkawa H.: "Different Clinical Characteristics of Aminoglycoside-Induced Profound Deafness with and without the 1555A->G Mitochondrial Mutation"ORL. 63. 25-30 (2001)
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[Publications] Namba A, Abe S, Shinkawa H, Kimberling WJ, Usami SI.: "enetic features of hearing loss associated with ear anomalies : PDS and EYA1 mutation analysis"J Hum Genet. 46(9). 518-521 (2001)
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[Publications] Abe S, Kelley PM, Kinberling WJ, Usami Si S: "Connexin 26 gene(GJB2)mutation modulates the severity of hearing loss associated with the 1555A-->G mitochondrial mutation"Am J Med Genet. 103(4). 334-338 (2001)
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[Publications] Fukuda S, Kuroda T, Chida E, Shimizu R, Usami S, Koda E, Abe S, Namba A, Kitamura K, Inuyama Y.: "A family affected by branchio-oto syndrome with EYA1 mutations"Auris Nasus Larynx. 28(Suppl). S7-S11 (2001)
