نتایج جستجو برای: large vestibular aqueduct

تعداد نتایج: 1043675  

Journal: :international clinical neurosciences journal 0
seifollah gholampour university of science and research branch islamic azad nasser fatouraee amirkabir university of technology amir saied seddighi shahid beheshti university of medical sciences saeed oraee yazdani m.d

b a c k ground: csf is a clear liquid that its mechanical properties are to a large extent similar to water properties. regarding the lack of a numerical index for diagnosis of diseases resulting from increased csf pressure such as hydrocephalus, evaluation of hydrodynamic conditions of csf in cerebral ventricular system is of great importance. methods: at first, the diagram of velocity in sylv...

2014
Sangeet Kumar Agarwal Satinder Singh Samarjit Singh Ghuman Shalabh Sharma Asish Kr. Lahiri

Introduction. Congenital sensorineural hearing loss is one of the most common birth defects with incidence of approximately 1 : 1000 live births. Imaging of cases of congenital sensorineural hearing loss is frequently performed in an attempt to determine the underlying pathology. There is a paucity of literature from India and for this reason we decided to conduct this study in Indian context t...

2017
Borum Sagong Jeong-In Baek Kyu-Yup Lee Un-Kyung Kim

OBJECTIVES We aimed to identify the causative mutation for siblings in a Korean family with nonsyndromic hearing loss (HL) and enlarged vestibular aqueduct (EVA). The siblings were a 19-year-old female with bilateral profound HL and an 11-year-old male with bilateral moderately severe HL. METHODS We extracted genomic DNA from blood samples of the siblings with HL, their parents, and 100 contr...

2016
Yalan Liu Lili Wang Yong Feng Chufeng He Deyuan Liu Xinzhang Cai Lu Jiang Hongsheng Chen Chang Liu Hong Wu Lingyun Mei

Enlarged vestibular aqueduct (EVA) is one of the most common congenital inner ear malformations and accounts for 1-12% of sensorineural deafness in children and adolescents. Multiple genetic defects contribute to EVA; therefore, early molecular diagnosis is critical for EVA patients to ensure that the most effective treatment strategies are employed. This study explored a new genetic diagnosis ...

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