Keilmann A - Search Results

1

Deficient membrane integration of the novel p.N14D-GJB2 mutant associated with non-syndromic hearing impairment.

Haack B, Schmalisch K, Palmada M, Böhmer C, Kohlschmidt N, Keilmann A, Zechner U, Limberger A, Beckert S, Zenner HP, Lang F, Kupka S. Haack B, et al. Among authors: keilmann a. Hum Mutat. 2006 Nov;27(11):1158-9. doi: 10.1002/humu.9464. Hum Mutat. 2006. PMID: 17041897

2

[Hearing loss in patients with Fabry disease].

Limberger A, Beck M, Delgado-Sanchez S, Keilmann A. Limberger A, et al. Among authors: keilmann a. HNO. 2007 Mar;55(3):185-9. doi: 10.1007/s00106-006-1454-z. HNO. 2007. PMID: 17004069 German.

3

[Congenital sensorineural deafness with microtia and Michel aplasia].

Läßig AK, Bartsch O, Zechner U, Keilmann A. Läßig AK, et al. Among authors: keilmann a. Laryngorhinootologie. 2015 Mar;94(3):182-3. doi: 10.1055/s-0034-1389976. Epub 2014 Nov 6. Laryngorhinootologie. 2015. PMID: 25376895 German. No abstract available.

4

Haploinsufficiency of 16.4 Mb from chromosome 22pter-q11.21 in a girl with unilateral conductive hearing loss.

Damatova N, Beyer V, Galetzka D, Schneider E, Napiontek U, Keilmann A, Zechner U, Bartsch O, Haaf T. Damatova N, et al. Among authors: keilmann a. Cytogenet Genome Res. 2009;125(3):241-7. doi: 10.1159/000230008. Epub 2009 Sep 4. Cytogenet Genome Res. 2009. PMID: 19738384

5

Disruption of the ATE1 and SLC12A1 Genes by Balanced Translocation in a Boy with Non-Syndromic Hearing Loss.

Vona B, Neuner C, El Hajj N, Schneider E, Farcas R, Beyer V, Zechner U, Keilmann A, Poot M, Bartsch O, Nanda I, Haaf T. Vona B, et al. Among authors: keilmann a. Mol Syndromol. 2014 Jan;5(1):3-10. doi: 10.1159/000355443. Epub 2013 Oct 4. Mol Syndromol. 2014. PMID: 24550759 Free PMC article.

6

[Diagnosis and therapy of auditory synaptopathy/neuropathy].

Moser T, Strenzke N, Meyer A, Lesinski-Schiedat A, Lenarz T, Beutner D, Foerst A, Lang-Roth R, von Wedel H, Walger M, Gross M, Keilmann A, Limberger A, Steffens T, Strutz J. Moser T, et al. Among authors: keilmann a. HNO. 2006 Nov;54(11):833-9. doi: 10.1007/s00106-006-1450-3. HNO. 2006. PMID: 17041780 Review. German.

7

[Magnetic resonance imaging in patients with magnetic hearing implants: overview and procedural management].

Nospes S, Mann W, Keilmann A. Nospes S, et al. Among authors: keilmann a. Radiologe. 2013 Nov;53(11):1026-32. doi: 10.1007/s00117-013-2570-x. Radiologe. 2013. PMID: 24113904 Review. German.

8

Hearing loss in Fabry disease: data from the Fabry Outcome Survey.

Hegemann S, Hajioff D, Conti G, Beck M, Sunder-Plassmann G, Widmer U, Mehta A, Keilmann A. Hegemann S, et al. Among authors: keilmann a. Eur J Clin Invest. 2006 Sep;36(9):654-62. doi: 10.1111/j.1365-2362.2006.01702.x. Eur J Clin Invest. 2006. PMID: 16919049 Free article.

9

[Cogan-I-syndrome. A rare differential diagnosis in progressive sensorineural hearing loss].

Massinger C, Keilmann A. Massinger C, et al. Among authors: keilmann a. HNO. 2003 Jan;51(1):66-70. doi: 10.1007/s00106-002-0707-8. HNO. 2003. PMID: 12557101 German.

10

Agalsidase alpha and hearing in Fabry disease: data from the Fabry Outcome Survey.

Hajioff D, Hegemann S, Conti G, Beck M, Sunder-Plassmann G, Widmer U, Mehta A, Keilmann A. Hajioff D, et al. Among authors: keilmann a. Eur J Clin Invest. 2006 Sep;36(9):663-7. doi: 10.1111/j.1365-2362.2006.01701.x. Eur J Clin Invest. 2006. PMID: 16919050

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