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Publikováno v:
Advances in oto-rhino-laryngology. 65
Performing stapes surgery for otosclerosis is known to be potentially irreversibly harmful to the inner ear function in about 1% of the cases. An early postoperative transient depression of the bone conduction thresholds is frequently detected after
Publikováno v:
Acta oto-rhino-laryngologica Belgica. 58(2)
Tympano-ossicular allografts are human transplants of the tympanic membrane alone or with the ossicles included. The authors review its use in their department since the introduction of the technique 40 years ago by J. Marquet. The advantages of the
Publikováno v:
Acta oto-rhino-laryngologica Belgica. 57(2)
Between 1991 and 2000, 154 cerebello-pontine angle (CPA) tumors were seen at the University ENT-department of the Sint-Augustinus Hospital, Antwerp. Amongst these, 127 were vestibular schwannomas detected by MR-imaging. Noteworthy is that in 5% of th
Autor:
P J, Govaerts, G, De Ceulaer, K, Daemers, K, Verhoeven, G, Van Camp, I, Schatteman, M, Verstreken, P J, Willems, T, Somers, F E, Offeciers
Publikováno v:
The American journal of otology. 19(6)
This study aimed to report on the audiologic findings of a nonsyndromic autosomal-dominant hearing loss of which the gene (DFNA 12) recently was found to map to chromosome 11q22-24. The study also aimed to propose and evaluate an algorithm based on t
Autor:
L, Van Laer, G, Van Camp, D, van Zuijlen, E D, Green, M, Verstreken, I, Schatteman, P, Van de Heyning, W, Balemans, P, Coucke, J H, Greinwald, R J, Smith, E, Huizing, P, Willems
Publikováno v:
European journal of human genetics : EJHG. 5(6)
A gene for an autosomal dominant form of progressive sensorineural hearing loss (DFNA5) was previously assigned by us to a 15-cM region on chromosome 7p15. In this study, the DFNA5 candidate region was refined to less than 2 cM, and completely cloned
Autor:
K, Verhoeven, G, Van Camp, P J, Govaerts, W, Balemans, I, Schatteman, M, Verstreken, L, Van Laer, R J, Smith, M R, Brown, P H, Van de Heyning, T, Somers, F E, Offeciers, P J, Willems
Publikováno v:
American journal of human genetics. 60(5)
We performed linkage analysis in a Belgian family with autosomal dominant midfrequency hearing loss, which has a prelingual onset and a nonprogressive course in most patients. We found LOD scores >6 with markers on chromosome 11q. Analysis of key rec
Publikováno v:
Acta oto-laryngologica. Supplementum. 526
A review of the literature on selective vestibular neurectomy for Meniere's disease is presented. The procedure is placed in historical context and current refinements of the technique are highlighted. In particular, the different methods of evaluati