A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairment von VAN LAER, L, COUCKE, P, FRANSEN, E, ROWLAND, J, CUCCI, R. A, SMITH, R. J. H, VAN CAMP, G, MUELLER, R. F, CAETHOVEN, G, FLOTHMANN, K, PRASAD, S. D, CHAMBERLIN, G. P, HOUSEMAN, M, TAYLOR, G. R, VAN DE HEYNING, C. M

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Quantification and Viability Assessment of Isolated Bovine Primordial and Primary Ovarian Follicles Retrieved Through a Standardized Biopsy Pick-Up Procedure von Aerts, JMJ, Martinez-Madrid, B, Flothmann, K, De Clercq, JBP, Van Aelst, S, Bols, PEJ

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A novel locus for autosomal dominant non-syndromic hearing loss, DFNA31, maps to chromosome 6p21.3 von Snoeckx, R L, Kremer, H, Ensink, R J H, Flothmann, K, de Brouwer, A, Smith, R J H, Cremers, C W R J, Van Camp, G

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Mutational spectrum of the WFS1 gene in Wolfram syndrome, nonsyndromic hearing impairment, diabetes mellitus, and psychiatric disease von Cryns, Kim, Sivakumaran, Theru A., Van den Ouweland, Jody M.W., Pennings, Ronald J.E., Cremers, Cor W.R.J., Flothmann, Kris, Young, Terry-Lynn, Smith, Richard J.H., Lesperance, Marci M., Camp, Guy Van

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Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss von Bespalova, I N, Van Camp, G, Bom, S J, Brown, D J, Cryns, K, DeWan, A T, Erson, A E, Flothmann, K, Kunst, H P, Kurnool, P, Sivakumaran, T A, Cremers, C W, Leal, S M, Burmeister, M, Lesperance, M M

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A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locus von Van Camp, Guy, Kunst, Henricus, Flothmann, Kris, McGuirt, Wyman, Wauters, Jan, Marres, Henri, Verstreken, Margriet, Bespalova, Irina N, Burmeister, Margit, Van de Heyning, Paul H, Smith, Richard J H, Willems, Patrick J, Cremers, Cor W R J, Lesperance, Marci M

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Determination of the carrier frequency of the common GJB2 (connexin-26) 35delG mutation in the Belgian population using an easy and reliable screening method von Storm, Katrien, Willocx, Sandra, Flothmann, Kris, Van Camp, Guy

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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

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A Novel Z-Score–Based Method to Analyze Candidate Genes for Age-Related Hearing Impairment von Fransen, Erik, Van Laer, Lut, Lemkens, Nele, Caethoven, Goele, Flothmann, Kris, Govaerts, Paul, Van de Heyning, Paul, Van Camp, Guy

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Perioperative Desensitization with IgA- and IgM-Enriched Human Immunoglobulins Allows Safe Lung Transplantation in Patients with Preformed Donor Specific Antibodies von Franz, M., Aburahma, K., Yablonski, P., Flöthmann, K., Bobylev, D., Schwerk, N., Sommer, W., Greer, M., Avsar, M., Welte, T., Falk, C., Haverich, A., Kühn, C., Warnecke, G., Salman, J., Ius, F.

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Impact of Donor Quality on Recipient Outcomes in Lung Transplantation: 10-year Single-Center Experience Using the Eurotransplant Lung Donor Score von Flöthmann, K., Salman, J., Aburahma, K., Siemeni, T., Franz, M., Greer, M., Avsar, M., Bobylev, D., Müller, C., Carlens, J., Schwerk, N., Niehaus, A., Sommer, W., Tudorache, I., Warnecke, G., Kühn, C., Haverich, A., Ius, F.

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Quantification and viability assessment of isolated bovine primordial and primary ovarian follicles retrieved through a standardized biopsy pick-up procedure von Aerts, J.M.J, Martinez-Madrid, B, Flothmann, K, De Clercq, J.B.P, Van Aelst, Stefan, Bols, P.E.J

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The ABCA4 2588G>C Stargardt mutation: single origin and increasing frequency from South-West to North-East Europe von Maugeri, Alessandra, Flothmann, Kris, Hemmrich, Nadine, Ingvast, Sofie, Jorge, Paula, Paloma, Eva, Patel, Reshma, Rozet, Jean-Michel, Tammur, Jaana, Testa, Francesco, Balcells, Susana, Bird, Alan C, Brunner, Han G, Hoyng, Carel B, Metspalu, Andres, Simonelli, Francesca, Allikmets, Rando, Bhattacharya, Shomi S, D'Urso, Michele, Gonzàlez-Duarte, Roser, Kaplan, Josseline, te Meerman, Gerard J, Santos, Rosário, Schwartz, Marianne, Van Camp, Guy, Wadelius, Claes, Weber, Bernhard H F, Cremers, Frans P M

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Is DFNA5 a susceptibility gene for age-related hearing impairment? von Van Laer, Lut, DeStefano, Anita L, Myers, Richard H, Flothmann, Kris, Thys, Sofie, Fransen, Erik, Gates, George A, Van Camp, Guy, Baldwin, Clinton T

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Vestibular dysfunction in the epistatic circler mouse is caused by phenotypic interaction of one recessive gene and three modifier genes von Cryns, Kim, Van Spaendonck, Michiel P, Flothmann, Kris, van Alphen, Arjan M, Van De Heyning, Paul H, Timmermans, Jean-Pierre, De Zeeuw, Chris I, Van Camp, Guy

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A common founder for the 35delG GJB2gene mutation in connexin 26 hearing impairment von Van Laer, L, Coucke, P, Mueller, R F, Caethoven, G, Flothmann, K, Prasad, S D, Chamberlin, G P, Houseman, M, Taylor, G R, Van de Heyning, C M, Fransen, E, Rowland, J, Cucci, R A, Smith, R J H, Van Camp, G

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A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairment von Van Laer, Lut, Coucke, Paul, Mueller, RF, Caethoven, G, Flothmann, K, Prasad, SD, Chamberlin, GP, Houseman, M, Taylor, GR, Van de Heyning, CM, Fransen, E, Rowland, J, Cucci, RA, Smith, RJH, Van Camp, G

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The topography of the HNCO(S 1) potential energy surface and its implications for photodissociation dynamics von Klossika, J.-J., Flöthmann, H., Beck, C., Schinke, R., Yamashita, K.

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Implementation of an integrated glucose POCT system von VAN HOOF, Viviane, CLUCKERS, Hugo, FLOTHMANN, Mark, NIJS, Lieve, COLPAERT, Filip, VERCAMMEN, Werner, BOLAIN, Dominique, VERHAEGHE, Vera, HENNEBEL, An, TRUYENS, Marleen, VAN LOOCK, Edith, ROMBOUTS, Pierre, MAES, Dirk, VAN ELVEN, Jan, LESAGE, Katrien

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Symmetry Breaking in Crossed Magnetic and Electric Fields von Neumann, C., Ubert, R., Freund, S., Flöthmann, E., Sheehy, B., Welge, K. H., Haggerty, M. R., Delos, J. B.

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