Perilymph pharmacokinetics of marker applied through a cochlear implant in guinea pigs von Salt, Alec, Hartsock, Jared, Gill, Ruth, Smyth, Daniel, Kirk, Jonathon, Verhoeven, Kristien

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Astrocytes regulate GluR2 expression in motor neurons and their vulnerability to excitotoxicity von Van Damme, Philip, Bogaert, Elke, Dewil, Maarten, Hersmus, Nicole, Kiraly, Dora, Scheveneels, Wendy, Bockx, Ilse, Braeken, Dries, Verpoorten, Nathalie, Verhoeven, Kristien, Timmerman, Vincent, Herijgers, Paul, Callewaert, Geert, Carmeliet, Peter, Van Den Bosch, Ludo, Robberecht, Wim

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Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease von Züchner, Stephan, Noureddine, Maher, Kennerson, Marina, Verhoeven, Kristien, Claeys, Kristl, Jonghe, Peter De, Merory, John, Oliveira, Sofia A, Speer, Marcy C, Stenger, Judith E, Walizada, Gina, Zhu, Danqing, Pericak-Vance, Margaret A, Nicholson, Garth, Timmerman, Vincent, Vance, Jeffery M

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Mutations in the Small GTP-ase Late Endosomal Protein RAB7 Cause Charcot-Marie-Tooth Type 2B Neuropathy von Verhoeven, Kristien, De Jonghe, Peter, Coen, Katrien, Verpoorten, Nathalie, Auer-Grumbach, Michaela, Kwon, Jennifer M., FitzPatrick, David, Schmedding, Eric, De Vriendt, Els, Jacobs, An, Van Gerwen, Veerle, Wagner, Klaus, Hartung, Hans-Peter, Timmerman, Vincent

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Acoustic Hearing After Murine Cochlear Implantation: Effects of Trauma and Implant Type von Kopelovich, Jonathan C., Robinson, Barbara K., Soken, Hakan, Verhoeven, Kristien J., Kirk, Jonathon R., Goodman, Shawn S., Hansen, Marlan R.

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Device Design Modifications Informed by In Vitro Testing of Bacterial Attachment Reduce Infection Rates of Cochlear Implants in Clinical Practice von Turnbull, Lynne, Leigh, Roger, Cavaliere, Rosalia, Osvath, Sarah R., Nolan, Laura M., Smyth, Daniel, Verhoeven, Kristien, Chole, Richard A., Whitchurch, Cynthia B.

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A deafness mutation isolates a second role for the tectorial membrane in hearing von Legan, P Kevin, Lukashkina, Victoria A, Goodyear, Richard J, Lukashkin, Andrei N, Verhoeven, Kristien, Van Camp, Guy, Russell, Ian J, Richardson, Guy P

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Localization of the Gene for the Intermediate Form of Charcot-Marie-Tooth to Chromosome 10q24.1-q25.1 von Verhoeven, Kristien, Villanova, Marcello, Rossi, Alessandro, Malandrini, Alessandro, De Jonghe, Peter, Timmerman, Vincent

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Recent advances in hereditary sensory and autonomic neuropathies von Verhoeven, Kristien, Timmerman, Vincent, Mauko, Barbara, Pieber, Thomas R, De Jonghe, Peter, Auer-Grumbach, Michaela

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Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2 von Züchner, Stephan, De Jonghe, Peter, Jordanova, Albena, Claeys, Kristl G., Guergueltcheva, Velina, Cherninkova, Sylvia, Hamilton, Steven R., Van Stavern, Greg, Krajewski, Karen M., Stajich, Jeffery, Tournev, Ivajlo, Verhoeven, Kristien, Langerhorst, Christine T., de Visser, Marianne, Baas, Frank, Bird, Thomas, Timmerman, Vincent, Shy, Michael, Vance, Jeffery M.

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An improved cochlear implant electrode array for use in experimental studies von Shepherd, Robert, Verhoeven, Kristien, Xu, Jin, Risi, Frank, Fallon, James, Wise, Andrew

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Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathy von Claeys, Kristl G., Züchner, Stephan, Kennerson, Marina, Berciano, José, Garcia, Antonio, Verhoeven, Kristien, Storey, Elsdon, Merory, John R., Bienfait, Henriette M. E., Lammens, Martin, Nelis, Eva, Baets, Jonathan, De Vriendt, Els, Berneman, Zwi N., De Veuster, Ilse, Vance, Jefferey M., Nicholson, Garth, Timmerman, Vincent, De Jonghe, Peter

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Recent advances in hereditary sensory and autonomic neuropathies von Verhoeven, Kristien, Timmerman, Vincent, Mauko, Barbara, Pieber, Thomas R, De Jonghe, Peter, Auer-Grumbach, Michaela

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Slowed Conduction and Thin Myelination of Peripheral Nerves Associated with Mutant Rho Guanine-Nucleotide Exchange Factor 10 von Verhoeven, Kristien, De Jonghe, Peter, Van de Putte, Tom, Nelis, Eva, Zwijsen, An, Verpoorten, Nathalie, De Vriendt, Els, Jacobs, An, Van Gerwen, Veerle, Francis, Annick, Ceuterick, Chantal, Huylebroeck, Danny, Timmerman, Vincent

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Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus von WAYNE, Sigrid, ROBERTSON, Nahid G, SMITH, Richard J. H, DECLAU, Frank, CHEN, Nancy, VERHOEVEN, Kristien, PRASAD, Sai, TRANEBJÄRG, Lisbeth, MORTON, Cynthia C, RYAN, Allen F, VAN CAMP, Guy

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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

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Experimental Charcot–Marie–Tooth type 1A: A cDNA microarrays analysis von Vigo, Tiziana, Nobbio, Lucilla, Hummelen, Paul Van, Abbruzzese, Michele, Mancardi, GianLuigi, Verpoorten, Nathalie, Verhoeven, Kristien, Sereda, Michael W., Nave, Klaus-Armin, Timmerman, Vincent, Schenone, Angelo

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Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathy von Claeys, Kristl, Züchner, Stephan, Kennerson, Marina, Berciano, José, Garcia, Antonio, Verhoeven, Kristien, Storey, Elsdon, Merory, John R, Bienfait, Henriette M.E, Lammens, Martin, Nelis, Eva, Baets, Jonathan, De Vriendt, Els, Berneman, Zwi N, De Veuster, Ilse, Vance, Jefferey M, Nicholson, Garth, Timmerman, Vincent, De Jonghe, Peter

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Astrocytes regulate GluR2 expression in motor neurons and their vulnerability to excitotoxicity von Van Damme, Philip, Bogaert, Elke, Dewil, Maarten, Hersmus, Nicole, Kiraly, Dora, Scheveneels, Wendy, Bockx, Ilse, Braeken, Dries, Verpoorten, Nathalie, Verhoeven, Kristien, Timmerman, Vincent, Herijgers, Paul, Callewaert, Geert, Carmeliet, Peter, Van den Bosch, Ludo, Robberecht, Wim

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Inner ear plug von Andersson, Marcus, Verhoeven, Kristien Johanna Maria, Smyth, Daniel, Treaba, Claudiu G, Dadd, Fysh

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