Association of Smoking and CFH and ARMS2 Risk Variants With Younger Age at Onset of Neovascular Age-Related Macular Degeneration von Lechanteur, Yara T. E, van de Camp, Patrick L, Smailhodzic, Dzenita, van de Ven, Johannes P. H, Buitendijk, Gabriëlle H. S, Klaver, Caroline C. W, Groenewoud, Joannes M. M, den Hollander, Anneke I, Hoyng, Carel B, Klevering, B. Jeroen

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Association of Smoking and CFH and ARMS2 Risk Variants With Younger Age at Onset of Neovascular Age-Related Macular Degeneration von Lechanteur, Yara T E, van de Camp, Patrick L, Smailhodzic, Dzenita, van de Ven, Johannes P H, Buitendijk, Gabriëlle H S, Klaver, Caroline C W, Groenewoud, Joannes M M, den Hollander, Anneke I, Hoyng, Carel B, Klevering, B Jeroen

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Treatment of Parkinson's disease with pergolide and relation to restrictive valvular heart disease von Van Camp, Guy, Flamez, Anja, Cosyns, Bernard, Weytjens, Caroline, Muyldermans, Luc, Van Zandijcke, Michel, De Sutter, Johan, Santens, Patrick, Decoodt, Pierre, Moerman, Christian, Schoors, Danny

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High Prevalence of Symptoms of Menière's Disease in three Families With a Mutation in the COCH Gene von Fransen, Erik, Verstreken, Margriet, Verhagen, Wim I. M., Wuyts, Floris L., Huygen, Patrick L.M., D'Haese, Patrick, Robertson, Nahid G., Morton, Cynthia C., McGuirt, Wyman T., Smith, Richard J. H., Declau, Frank, Van de Heyning, Paul H., Van Camp, Guy

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Familial Aggregation of Pure Tone Hearing Thresholds in an Aging European Population von Hendrickx, Jan-Jaap, Huyghe, Jeroen R, Topsakal, Vedat, Demeester, Kelly, Wienker, Thomas F, Laer, Lut Van, Eyken, Els Van, Fransen, Erik, Mäki-Torkko, Elina, Hannula, Samuli, Parving, Agnete, Jensen, Mona, Tropitzsch, Anke, Bonaconsa, Amanda, Mazzoli, Manuela, Espeso, Angeles, Verbruggen, Katja, Huyghe, Joke, Huygen, Patrick L.M, Kremer, Hannie, Kunst, Sylvia J, Diaz-Lacava, Amalia N, Steffens, Michael, Pyykkö, Ilmari, Dhooge, Ingeborg, Stephens, Dafydd, Orzan, Eva, Pfister, Markus H.F, Bille, Michael, Sorri, Martti, Cremers, Cor W.R.J, Camp, Guy Van, de Heyning, Paul Van

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Part 9: Acute coronary syndromes: 2010 International Consensus on Cardiopulmonary Resuscitation and Emergency Cardiovascular Care Science With Treatment Recommendations von O'Connor, Robert E, Bossaert, Leo, Arntz, Hans-Richard, Brooks, Steven C, Diercks, Deborah, Feitosa-Filho, Gilson, Nolan, Jerry P, Vanden Hoek, Terry L, Walters, Darren L, Wong, Aaron, Welsford, Michelle, Woolfrey, Karen

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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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Nonsyndromic hearing impairment is associated with a mutation in DFNA5 von Van Camp, Guy, Laer, Lut Van, Huizing, Egbert H, Verstreken, Margriet, Zuijlen, Diederick van, Wauters, Jan G, Bossuyt, Paul J, Van de Heyning, Paul, McGuirt, Wyman T, Smith, Richard J.H, Willems, Patrick J, Legan, P. Kevin, Richardson, Guy P

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Two Frequent Missense Mutations in Pendred Syndrome von Van Hauwe, Peter, Everett, Lorraine A., Coucke, Paul, Scott, Daryl A., Kraft, Michelle L., Ris-Stalpers, Carrie, Bolder, Cuny, Otten, Barto, de Vijlder, Jan J.M., Dietrich, Nicole L., Ramesh, Arabandi, Srisailapathy, Srikumari C. R., Parving, Agnete, Cremers, Cor W. R. J., Willems, Patrick J., Smith, Richard J. H., Green, Eric D., Van Camp, Guy

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Effect of maternal multiple micronutrient supplements on cord blood hormones: a randomized controlled trial von Roberfroid, Dominique, Huybregts, Lieven, Lanou, Hermann, Henry, Marie-Claire, Meda, Nicolas, Kolsteren f, Patrick

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Part 9: Acute coronary syndromes: 2010 International Consensus on Cardiopulmonary Resuscitation and Emergency Cardiovascular Care Science with Treatment Recommendations von Bossaert, Leo, O'Connor, Robert E, Arntz, Hans-Richard, Brooks, Steven C, Diercks, Deborah, Feitosa-Filho, Gilson, Nolan, Jerry P, Hoek, Terry L Vanden, Walters, Darren L, Wong, Aaron, Welsford, Michelle, Woolfrey, Karen

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A common ancestor for COCH related cochleovestibular (DFNA9) patients in Belgium and The Netherlands bearing the P51S mutation von FRANSEN, ERIK, VERSTREKEN, MARGRIET, BOM, STEVEN J H, LEMAIRE, FRANÇOIS, KEMPERMAN, MARTIJN H, DE KOK, YVETTE J M, WUYTS, FLORIS L, VERHAGEN, WIM I M, HUYGEN, PATRICK L M, MCGUIRT, WYMAN T, SMITH, RICHARD J H, VAN MALDERGEM, LIONEL, DECLAU, FRANK, CREMERS, COR W R J, VAN DE HEYNING, PAUL H, CREMERS, FRANS P M, VAN CAMP, GUY

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Localization of a gene for non-syndromic hearing loss (DFNA5) to chromosome 7p15 von Camp, Guy Van, Coucke, Paul, Balemans, Wendy, Van Velzen, Désirée, Van de Bilt, Caroline, Van Laer, Lut, Smith, Richard J.H., Fukushima, Kunihiro, Padberg, George W., Frants, Rune R., Heyning, Paul Van de, Smith, Shelley D., Huizing, Egbert H., Willems, Patrick J.

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A mutational hot spot in the KCNQ4 gene responsible for autosomal dominant hearing impairment von Van Camp, Guy, Coucke, Paul J., Akita, Jiro, Fransen, Erik, Abe, Satoko, De Leenheer, Els M.R., Huygen, Patrick L.M., Cremers, Cor W.R.J., Usami, Shin-Ichi

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Further Delineation of the DFNA5 Phenotype: Results of Speech Recognition Tests von Van Zuijlen, Diederick A., Huygen, Patrick L. M., De Leenheer, Els M. R., Van Laer, Lut, Huizing, Egbert H., Van Camp, Guy, Cremers, W. R. J.

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Longitudinal and Cross-Sectional Phenotype Analysis in a New, Large Dutch DFNA2/KCNQ4 Family von De Leenheer, Els M. R., Huygen, Patrick L. M., Coucke, Paul J., Admiraal, Ronald J. C., Van Camp, Guy, Cremers, Cor W. R. J.

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The phenotype of the first otosclerosis family linked to OTSC5 von Pauw, Robert J, De Leenheer, Els M R, Van Den Bogaert, Kris, Huygen, Patrick L M, Van Camp, Guy, Joosten, Frank B M, Cremers, Cor W R J

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MASA syndrome is due to mutations in the neural cell adhesion gene L1CAM von Vits, Lieve, Van Camp, Guy, Coucke, Paul, Fransen, Erik, De Boulle, Kristel, Reyniers, Edwin, Korn, Bernhard, Poustka, Annemarie, Wilson, Golder, Schrander-Stumpel, Connie, Winter, Robin M, Schwartz, Charles, Willems, Patrick J

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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

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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

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