✦ LIBER ✦

Sensorineural hearing loss caused by nonsteroldal-induced aseptic meningitis

✍ Scribed by Steven P. Davison; Mitchell S. Marion

Book ID: 117402340
Publisher: SAGE Publications
Year: 1996
Tongue: English
Weight: 96 KB
Volume: 115
Category: Article
ISSN: 0194-5998
DOI: 10.1016/s0194-5998(96)80981-8

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Cochlear implantation for severe sensori

Cochlear implantation for severe sensorineural hearing loss caused by lightning

✍ Nam-Suk Myung; Il-Woo Lee; Eui-Kyung Goh; Soo-Keun Kong 📂 Article 📅 2012 🏛 Elsevier Science 🌐 English ⚖ 592 KB

Sudden onset sensorineural hearing loss

Sudden onset sensorineural hearing loss caused by meningeal carcinomatosis secondary to occult malignancy: Report of two cases

✍ Maria Raffaella Marchese; Carmelo La Greca; Guido Conti; Gaetano Paludetti 📂 Article 📅 2010 🏛 Elsevier Science 🌐 English ⚖ 525 KB

Bilateral sudden sensorineural hearing l

Bilateral sudden sensorineural hearing loss caused by alcohol abuse and heroin sniffing

✍ Stavros Antonopoulos; Dimitrios G. Balatsouras; Sofia Kanakaki; Athina Dona; Chr 📂 Article 📅 2012 🏛 Elsevier Science 🌐 English ⚖ 636 KB

Sensorineural hearing loss caused by cyt

Sensorineural hearing loss caused by cytomegalovirus infection as a risk factor for epilepsy

✍ D. Dunin-Waogon;sowicz; S. Jóźwiak; M. Radziszewska-Konopka 📂 Article 📅 2008 🏛 Elsevier Science 🌐 English ⚖ 43 KB

Sensorineural hearing loss caused by mit

Sensorineural hearing loss caused by mitochondrial dna mutations: Special reference to the a1555g mutation

✍ Shin-Ichi Usami; Satoko Abe; Hideichi Shinkawa; William J. Kimberling 📂 Article 📅 1998 🏛 Elsevier Science 🌐 English ⚖ 239 KB

Optic atrophy and sensorineural hearing

Optic atrophy and sensorineural hearing loss in a family caused by an R445H OPA1 mutation

✍ Chunmei Li; Gregory Kosmorsky; Kang Zhang; Bradley J. Katz; Jian Ge; Elias I. Tr 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 120 KB 👁 1 views

## Abstract Autosomal dominant optic atrophy (ADOA) is the most common form of inherited optic atrophy. Four genetic loci have been associated with ADOA: OPA1, OPA2, OPA3, and OPA4. Out of these four loci, only one gene has been identified, __OPA1.__ We previously described a unique syndrome of opt