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Anatomie surdi nati secto: Bononiensc scientarium et artium institu atque academia commenterii
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1842373263
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AJR Am J Roentgenol
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Okumura T, Takahashi H, Honjo I, Naito Y, Takagi A, Tuji J, Ito J: Sensorineural hearing loss in patients with large vestibular aqueduct Laryngoscope 1995, 105:289-294.
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Advanced techniques in magnetic resonance imaging in the evaluation of the large endolymphatic duct and sac syndrome
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Hamsberger HR, Dahlen RT, Shelton C, Gray SD, Parkin JL: Advanced techniques in magnetic resonance imaging in the evaluation of the large endolymphatic duct and sac syndrome. Laryngoscope 1995, 105:1037-1042.
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Hamsberger, H.R.1
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Parkin, J.L.5
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0031031371
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Overlapping thin section fast spin echo MR of the large vestibular aqueduct syndrome: Comparison with CT
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Dahlen RT, Hamsberger HR, Gray SD, Shelton C, Allen R, Parkin JL: Overlapping thin section fast spin echo MR of the large vestibular aqueduct syndrome: comparison with CT. AJNR Am J Neuroradiol 1997, 18:67-75. This paper reviews the normal dimensions of the duct and sac and explains the method of measurement essential for making a diagnosis. The complimentary nature of CT and MRI in LVAS and other associated inner ear anomalies is well described. As a screening tool, fast spin echo MRI alone is adequate to diagnose or exclude LVAS with confidence.
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AJNR Am J Neuroradiol
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Dahlen, R.T.1
Hamsberger, H.R.2
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Large vestibular aqueduct syndrome and stapes fixation
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Shirazi A, Fenton JE, Fagan PA: Large vestibular aqueduct syndrome and stapes fixation. J Laryngol Otol 1994, 108:989-990.
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Coyle B, Coffey R, Armour JAL, Gausden E, Hochberg Z, Grossman A, Britton K, Pembrey, Reardon W, Trembath R: Pendred syndrome (goitre and sensorineural hearing loss) maps to chromosome 7 in the region containing the nonsyndromic deafness gene DFNB4. War Genet 1996, 12:421-423.
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Griffith AJ, Arts HA, Downs C, Innis JW, Shepard NT, Sheldon S, Gebarski SS: Familial large vestibular aqueduct syndrome. Laryngoscope 1996, 106:960-965. A description of familial LVAS. This important observation has implications both for research into the underlying molecular pathogenesis and genetic counseling of parents with children who have LVAS.
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Smith RJH: Commentary. Am J Otol 1997, 18:106-107. A bold and well-written short commentary on the paper by Wilson et al. (Am J Otol 1997, 18:101-106). Smith discusses the controversy regarding the results of surgical obliteration of the endolymphatic sac in LVAS. He argues that the results of surgery reported by Wilson et al. merely reflect the natural history of the disease and he advises against surgery in these patients.
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Am J Otol
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Smith, R.J.H.1
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