Hearing in Children with Congenital Cytomegalovirus Infection: Results of a Longitudinal Study von Goderis, Julie, MD, Keymeulen, Annelies, MD, Smets, Koenraad, MD, PhD, Van Hoecke, Helen, MD, PhD, De Leenheer, Els, MD, PhD, Boudewyns, An, MD, PhD, Desloovere, Christian, MD, PhD, Kuhweide, Rudolf, MD, Muylle, Marie, MSc, Royackers, Liesbeth, MSc, Schatteman, Isabelle, MD, Dhooge, Ingeborg, MD, PhD

Volltext

A wide range of protective and predisposing variants in aggrecan influence the susceptibility for otosclerosis von Højland, Allan Thomas, Tavernier, Lisse J. M., Schrauwen, Isabelle, Sommen, Manou, Topsakal, Vedat, Schatteman, Isabelle, Dhooge, Ingeborg, Huber, Alex, Zanetti, Diego, Kunst, Henricus P. M., Hoischen, Alexander, Petersen, Michael B., Van Camp, Guy, Fransen, Erik

Volltext

Risk Factors for hearing loss at birth in newborns with congenital cytomegalovirus infection von De Cuyper, Elise, Acke, Frederic, Keymeulen, Annelies, De Leenheer, Els, Van Hoecke, Helen, Padalko, Elizaveta, Boudewyns, An, Gilles, Annick, Muylle, Marie, Kuhweide, Rudolf, Royackers, Liesbeth, Desloovere, Christian, Verstreken, Margriet, Schatteman, Isabelle, Dhooge, Ingeborg

Volltext

Autosomal Dominantly Inherited GREB1L Variants in Individuals with Profound Sensorineural Hearing Impairment von Schrauwen, Isabelle, Liaqat, Khurram, Schatteman, Isabelle, Bharadwaj, Thashi, Nasir, Abdul, Acharya, Anushree, Ahmad, Wasim, Van Camp, Guy, Leal, Suzanne M

Volltext

Insufficient evidence for a role of SERPINF1 in otosclerosis von Valgaeren, Hanne, Sommen, Manou, Beyens, Matthias, Vandeweyer, Geert, Schrauwen, Isabelle, Schepers, Anne, Schatteman, Isabelle, Topsakal, Vedat, Dhooge, Ingeborg, Kunst, Henricus, Zanetti, Diego, Huber, Alexander M., Hoischen, Alexander, Fransen, Erik, Van Camp, Guy

Volltext

Insufficient evidence for a role of SERPINF1 in otosclerosis von Valgaeren, Hanne, Sommen, Manou, Beyens, Matthias, Vandeweyer, Geert, Schrauwen, Isabelle, Schepers, Anne, Schatteman, Isabelle, Topsakal, Vedat, Dhooge, Ingeborg, Kunst, Henricus, Zanetti, Diego, Huber, Alexander M, Hoischen, Alexander, Fransen, Erik, Van Camp, Guy

Volltext

Congenital cytomegalovirus infection registry in flanders: opportunities and pitfalls von Keymeulen, Annelies, De Leenheer, Els, Goderis, Julie, Dhooge, Ingeborg, Smets, Koenraad, Boudewyns, An, Casaer, Alexandra, Cossey, Veerle, De Sloover, Christian, Kuhweide, Rudolf, Mahieu, Ludo, Naulaers, Gunnar, Royackers, Liesbeth, Schatteman, Isabelle, Van Mol, Christine

Volltext

Outcome of cochlear implantation at different ages from 0 to 6 years von GOVAERTS, Paul J, DE BEUKELAER, Carina, DAEMERS, Kristin, DE CEULAER, Geert, YPERMAN, Marjan, SOMERS, Thomas, SCHATTEMAN, Isabelle, OFFECIERS, F. Erwin

Volltext

Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment von Verhoeven, Kristien, Laer, Lut Van, Kirschhofer, Karin, Legan, P. Kevin, Hughes, David C., Schatteman, Isabelle, Verstreken, Margriet, Hauwe, Peter Van, Coucke, Paul, Chen, Achih, Smith, Richard J.H., Somers, Thomas, Offeciers, F. Erwin, Heyning, Paul Van de, Richardson, Guy P., Wachtler, Franz, Kimberling, William J., Willems, Patrick J., Govaerts, Paul J., Camp, Guy Van

Volltext

Mutations in the KCNQ4 Gene Are Responsible for Autosomal Dominant Deafness in Four DFNA2 Families von Coucke, Paul J., Van Hauwe, Peter, Kelley, Philip M., Kunst, Henricus, Schatteman, Isabelle, Van Velzen, Désirée, Meyers, Johan, Ensink, Robbert J., Verstreken, Margriet, Declau, Frank, Marres, Henri, Kastury, Kumar, Bhasin, Shalender, McGuirt, Wyman T., Smith, Richard J. H., Cremers, Cor W.R.J., Van de Heyning, Paul, Willems, Patrick J., Smith, Shelley D., Van Camp, Guy

Volltext

A Second Gene for Otosclerosis, OTSC2, Maps to Chromosome 7q34-36 von Van Den Bogaert, Kris, Govaerts, Paul J., Schatteman, Isabelle, Brown, Matthew R., Caethoven, Goele, Offeciers, F.Erwin, Somers, Thomas, Declau, Frank, Coucke, Paul, de Heyning, Paul Van, Smith, Richard J.H., Van Camp, Guy

Volltext

Transmeatal Procurement of Allograft Tympano-Ossicular Systems: Preliminary Report (Alternative to the intracranial bone plug technique by Schuknecht) von van Rompaey, Vincent, van Dinther, Joost, Somers, Thomas, Vanhoof, Luc, Maes, Maggie, Schatteman, Isabelle, Offeciers, Erwin

Volltext

Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutations von CRYNS, Kim, PFISTER, Markus, KUPKA, Susan, BLIN, Nikolaus, NÜRNBERG, Peter, THIELE, Holger, DE HEYNING, Paul H, REARDON, William, STEPHENS, Dafydd, CREMERS, Cor W. R. J, SMITH, Richard J. H, VAN CAMP, Guy, PENNINGS, Ronald J. E, BOM, Steven J. H, FLOTHMANN, Kris, CAETHOVEN, Goele, KREMER, Hannie, SCHATTEMAN, Isabelle, KÖLN, Karen A, TOTH, Timea

Volltext

Middle and inner ear malformations in velocardiofacial syndrome von Devriendt, Koenraad, Swillen, Ann, Schatteman, Isabelle, Lemmerling, Marc, Dhooge, Ingeborg

Volltext

The Use of Malleus Allografts in Ossiculoplasty von Vercruysse, Jean-Philippe, Offeciers, F. Erwin, Somers, Thomas, Schatteman, Isabelle, Govaerts, Paul J.

Volltext

A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24 von VERHOEVEN, K, VAN CAMP, G, SOMERS, T, OFFECIERS, F. E, WILLEMS, P. J, GOVAERTS, P. J, BALEMANS, W, SCHATTEMAN, I, VERSTREKEN, M, VAN LAER, L, SMITH, R. J. H, BROWN, M. R, VAN DE HEYNING, P. H

Volltext

A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2) von Lench, N J, Markham, A F, Mueller, R F, Kelsell, D P, Smith, R J, Willems, P J, Schatteman, I, Capon, H, Van De Heyning, P J, Van Camp, G

Volltext

Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairment von VERHOEVEN, K, FAGERHEIM, T, TRANEBJÄRG, L, SMITH, R. J. H, VAN CAMP, G, PRASAD, S, WAYNE, S, DE CLAU, F, BALEMANS, W, VERSTREKEN, M, SCHATTEMAN, I, SOLEM, B, VAN DE HEYNING, P

Volltext

A new autosomal-dominant locus (DFNA12) is responsible for a nonsyndromic, midfrequency, prelingual and nonprogressive sensorineural hearing loss von GOVAERTS, P. J, DE CEULAER, G, DAEMERS, K, VERHOEVEN, K, VAN CAMP, G, SCHATTEMAN, I, VERSTREKEN, M, WILLEMS, P. J, SOMERS, T, OFFECIERS, F. E

Volltext

Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer(UCN) gene von Verhoeven, K, Ensink, R J, Tiranti, V, Huygen, P L, Johnson, D F, Schatteman, I, Van Laer, L, Verstreken, M, Van de Heyning, P, Fischel-Ghodsian, N, Zeviani, M, Cremers, C W, Willems, P J, Van Camp, G

Volltext