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Original Article

Familial incidence of streptomycin hearing loss and hereditary weakness of the cochlea

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Pages 315-322 | Published online: 07 Jul 2009

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Iwao Ohtani, Kohsei Ohtsuki, Tohru Aikawa, Takeo Omata, Jin Ouchi & Takeo Saito. (1982) Individual Variation and Mechanism of Kanamycin Ototoxicity in Rabbits. Acta Oto-Laryngologica 94:1-6, pages 413-419.
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. (1981) Aminoglycoside-Induced Cochlear Pathology in Man. Acta Oto-Laryngologica 92:sup383, pages 1-19.
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Articles from other publishers (20)

Nevin Hatipoğlu, Emin Sami Arısoy & Flor Munoz-Rivas. 2023. Hearing Loss in Congenital, Neonatal and Childhood Infections. Hearing Loss in Congenital, Neonatal and Childhood Infections 1065 1094 .
Hyo-Jung Kim, Jin-Ok Lee & Ji-Soo Kim. (2021) Protective Effects of Deferoxamine on Vestibulotoxicity in Gentamicin-Induced Bilateral Vestibulopathy Rat Model. Frontiers in Neurology 12.
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Takashi Tsuiki. (2010) Streptomycin hearing loss and genetic predisposition to hearing loss of cochlear origin. AUDIOLOGY JAPAN 53:6, pages 653-663.
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Nathan Fischel-Ghodsian. (2005) Genetic factors in aminoglycoside toxicity. Pharmacogenomics 6:1, pages 27-36.
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Nathan Fischel-Ghodsian. 2002. Genetics of Auditory Disorders. Genetics of Auditory Disorders 228 246 .
Christian Kubisch, Hanno Bolz & Andreas Gal. 2000. Monogen bedingte Erbkrankheiten 2. Monogen bedingte Erbkrankheiten 2 115 149 .
NATHAN FISCHEL‐GHODSIAN. (2006) Genetic Factors in Aminoglycoside Toxicity. Annals of the New York Academy of Sciences 884:1, pages 99-109.
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Nathan Fischel-Ghodsian. (1999) Mitochondrial deafness mutations reviewed. Human Mutation 13:4, pages 261-270.
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Shin-Ichi Usami, Satoko Abe, Hideichi Shinkawa & William J. Kimberling. (1998) Sensorineural hearing loss caused by mitochondrial dna mutations. Journal of Communication Disorders 31:5, pages 423-435.
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Takashi Tsuiki, Kazuo Murai, Ken Kitamura, Seiko Murai & Yuya Tamagawa. (2016) Audiologic Features of Hearing Loss Due to the 1,555 Mutation of Mitochondrial DNA. Annals of Otology, Rhinology & Laryngology 106:8, pages 643-648.
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Shin-ichi Usami, Satoko Abe, Miyo Kasai, Hideichi Shinkawa, Benjamin Moeller, Judy B. Kenyon & William J. Kimberling,. (1997) Genetic and Clinical Features of Sensorineural Hearing Loss Associated With the 1555 Mitochondrial Mutation. The Laryngoscope 107:4, pages 483-490.
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D N Hu, W Q Qui, B T Wu, L Z Fang, F Zhou, Y P Gu, Q H Zhang, J H Yan, Y Q Ding & H Wong. (1991) Genetic aspects of antibiotic induced deafness: mitochondrial inheritance.. Journal of Medical Genetics 28:2, pages 79-83.
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T. Midtvedt. 1991. 266 275 .
Koichiro Higashi. (2008) Unique inheritance of streptomycininduced deafness. Clinical Genetics 35:6, pages 433-436.
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Patricia A. Leake & Gary T. Hradek. (1988) Cochlear pathology of long term neomycin induced deafness in cats. Hearing Research 33:1, pages 11-33.
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L. Keßler. 1988. HNO Praxis Heute. HNO Praxis Heute 1 18 .
E. Lehnhardt. 1984. Verhandlungsbericht 1984 der Deutschen Gesellschaft für Hals- Nasen- Ohren-Heilkunde, Kopf- und Hals-Chirurgie. Verhandlungsbericht 1984 der Deutschen Gesellschaft für Hals- Nasen- Ohren-Heilkunde, Kopf- und Hals-Chirurgie 58 218 .
KENNETH R. HENRY. 1983. Development of Auditory and Vestibular Systems. Development of Auditory and Vestibular Systems 273 308 .
Anthony F. Jahn & Arnold M. Noyek. (1981) Hereditary Hearing Losses with Delayed Onset: Mechanisms of Expression. Otolaryngologic Clinics of North America 14:1, pages 59-64.
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F. Clarke Fraser. 1977. General Principles and Etiology. General Principles and Etiology 445 463 .

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