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2 ta on the surgical management of symptomatic otosclerosis and compared them with data from the litera
5 ly that was ascertained to have nonsyndromic otosclerosis but was subsequently found to have a congen
6 were found in seven patients in our familial otosclerosis cohort; three are missense mutations predic
9 d a large multi-generational family in which otosclerosis has been inherited in an autosomal dominant
10 we report a meta-analysis of GWAS studies of otosclerosis in three population-based biobanks comprisi
15 apes is usually progressive and secondary to otosclerosis, it may present congenitally, with other sk
17 d that SERPINF1-012 expression is reduced in otosclerosis patients with and without SERPINF1 mutation
18 ients with sporadic or familial nonsyndromic otosclerosis should be evaluated for mild features of th
19 ese results suggest that in France, treating otosclerosis surgically is slightly less expensive over
20 6 affected persons have surgically confirmed otosclerosis; the remaining nine have a conductive heari
21 our families exhibiting dominantly inherited otosclerosis to identify 23 candidate variants (reduced
22 The cost-effectiveness and budget impact of otosclerosis treatments have never been studied in Europ
23 ixation of the malleus and/or the incus with otosclerosis were classified into two different surgical