Keilmann A - Search Results

1

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

2

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.

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

[Stroboscopy findings: a comparison of flexible CCD-videostroboscopy and rigid stroboscopy].

Nospes S, Kuhr K, Napiontek U, Keilmann A. Nospes S, et al. Among authors: keilmann a. Laryngorhinootologie. 2011 Apr;90(4):218-23. doi: 10.1055/s-0031-1271631. Epub 2011 Feb 10. Laryngorhinootologie. 2011. PMID: 21312156 German.

5

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

6

[Acoustic schwannoma with progressive hearing loss in children. A case report].

Massinger C, Gawehn J, Keilmann A. Massinger C, et al. Among authors: keilmann a. Laryngorhinootologie. 2003 Feb;82(2):92-6. doi: 10.1055/s-2003-37728. Laryngorhinootologie. 2003. PMID: 12624835 German.

7

[Vohwinkel syndrome. Hearing loss and keratoderma on the hands and feet].

Dippold S, Butsch F, Schopf R, Keilmann A. Dippold S, et al. Among authors: keilmann a. HNO. 2013 Jul;61(7):617-9. doi: 10.1007/s00106-012-2607-x. HNO. 2013. PMID: 23247752 German.

8

[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.

9

[Hearing disorders in aphasia].

Läßig AK, Kreter S, Nospes S, Keilmann A. Läßig AK, et al. Among authors: keilmann a. Laryngorhinootologie. 2013 Aug;92(8):531-5. doi: 10.1055/s-0033-1347201. Epub 2013 Jul 30. Laryngorhinootologie. 2013. PMID: 23900924 German.

10

[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.

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