deafness造句
91 Objective To search responsible nuclear genes for matrilineal non - syndromic deafness.
92 So that, dextran 40 low molecular, Salviae miltiorrhizae compositus and carbogen were used to treat the 85 patients with sudden deafness and acquired a better result.
93 Have persistent headaches, accompanied by nausea, vomiting or visual disorder, or nasal bleeding, dizziness, tinnitus, deafness and other symptoms.
94 Conclusion 45 positive loci obtained from this family may be as the candidate matrilineal non - syndromic deafness.
95 A common type of inner ear deafness seen in adults is that due to acoustic trauma.
96 Except for the felicitous pretense of deafness I had not tried to pretend anything.
97 Discharging an un silenced firearm in a room can cause temporary deafness.
98 Results Tubercular otitis media and mastoiditis was mainly characterized by otorrhea, big perforation of tympanic membrane, abundant pale or red granulation, heavy deafness.
99 A mostly home-taught member of a Scottish family interested in issues of speech and deafness, Bell followed his father, Alexander Melville Bell, as a teacher of the deaf.
100 Conclusion Auricular point plaster therapy plus routine treatment can promote early recovery form sudden deafness.
101 Keratitis, ichthyosis , and deafness syndrome ( KID syndrome ) is a rare congenital disorder disease.
102 Description: Statutory body for providing compensation to persons who have suffered noise-induced deafness due to employment.
103 Thekey of preventing acquired deafness was to prohibit the misapplication of ototoxic antibiotics.
104 It pointed mouth big ears, long body, short behind trail a long tail, systemic palm red, black, white tail pointed deafness, tail base has a hole, can emit a pungent odor.
105 It's a genetic trait that causes deafness at an early age.
106 Conclusion:Vinpocetine coalition citicoline sodium to treat sudden deafness has obvious effect, clinical care is very important during therapy sudden deafness.
107 G79A heterozygosis compounded with A341G heterozygosis and G79A homozygosis compounded with A341G homozygosis were found in deafness students and their family members with normal hearing.
108 This is perhaps the proper place to relate the history of Grandet's stammer and deafness.
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