The positive modulator of AMPA receptors, S 47445, improved behavior, cognitive, neurochemical and synaptic proteins modifications induced by prenatal restraint stress von Bretin, S, Maccari, S, Morley-Fletcher, S, Mairesse, J, Vancamp, G, Pittaluga, A, Nicoletti, F, Mocaer, E

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Angiotensin-Converting Enzyme 2 (ACE2) and ACE Activities Display Tissue-Specific Sensitivity to Undernutrition-Programmed Hypertension in the Adult Rat von Rivière, Guillaume, Michaud, Annie, Breton, Christophe, VanCamp, Gilles, Laborie, Christine, Enache, Mihaela, Lesage, Jean, Deloof, Sylvie, Corvol, Pierre, Vieau, Didier

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P3375 Valvular heart disease in patients with Parkinsons disease treated with pergolide von VANCAMP, G

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Nonsyndromic hearing impairment : Unparalleled heterogeneity von VAN CAMP, G, WILLEMS, P. J, SMITH, R. J. H

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Non-syndromic autosomal dominant sensorineural hearing loss: a new field of research von Kunst, H, Marres, H, Van Camp, G, Cremers, C

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L1-Associated Diseases: Clinical Geneticists Divide, Molecular Geneticists Unite von Fransen, Erik, Van Camp, Guy, Vits, Lieve, Willems, Patrick J.

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Second harmonic transthoracic echocardiography: the new reference screening method for the detection of patent foramen ovale von Daniëls, Cathy, Weytjens, Caroline, Cosyns, Bernard, Schoors, Danny, De Sutter, Johan, Paelinck, Bernard, Muyldermans, Luc, Van Camp, Guy

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CRASH syndrome: clinical spectrum of corpus callosum hypoplasia, retardation, adducted thumbs, spastic paraparesis and hydrocephalus due to mutations in one single gene, L1 von Fransen, E, Lemmon, V, Van Camp, G, Vits, L, Coucke, P, Willems, P 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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Relation between patent foramen ovale and unexplained stroke von Van Camp, Guy, Schulze, Dominique, Cosyns, Bernard, Vandenbossche, Jean-Luc

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Endothelin-3 Gene Mutations in Isolated and Syndromic Hirschsprung Disease von Bidaud, Christelle, Salomon, Rémi, Van Camp, Guy, Pelet, Anna, Attié, Tania, Eng, Charis, Bonduelle, Maryse, Amiel, Jeanne, Nihoul-Fékété, Claire, Willems, Patrick J., Munnich, Arnold, Lyonnet, Stanislas

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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 Novel Locus for Autosomal Dominant Nonsyndromic Hearing Loss, DFNA13, Maps to Chromosome 6p von Brown, M.R., Tomek, M.S., Van Laer, L., Smith, S., Kenyon, J.B., Van Camp, G., Smith, R.J.H.

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A Gene for Autosomal Dominant Late-Onset Progressive Non-Syndromic Hearing Loss, DFNA10, Maps to Chromosome 6 von O'Neill, Marsha E., Marietta, Jacquie, Nishimura, Darryl, Wayne, Sigrid, Van Camp, Guy, Van Laer, Lut, Negrini, Clelia, Wilcox, Edward R., Chen, Achih, Fukushima, Kunihiro, Ni, Li, Sheffield, Val C., Smith, Richard J. H.

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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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A duplication in the L1CAM gene associated with X–linked hydrocephalus von Camp, Guy Van, Vits, Lieve, Coucke, Paul, Lyonnet, Stanislas, Schrander-Stumpel, Connie, Darby, John, Holden, Jeanette, Munnich, Arnold, Willems, Patrick J.

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X-linked hydrocephalus and MASA syndrome present in one family are due to a single missense mutation in exon 28 of the L1CAM gene von Fransen, Erik, Schrander-Stumpel, Connle, Vits, Lieve, Coucke, Paul, Van Camp, Guy, Willems, Patrick J.

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A locus-specific mutation database for the neural cell adhesion molecule L1CAM (Xq28) von Van Camp, Guy, Fransen, Erik, Vits, Lieve, Raes, Geert, Willems, Patrick J.

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An autosomal recessive nonsyndromic form of sensorineural hearing loss maps to 3p-DFNB6 von Fukushima, K, Ramesh, A, Srisailapathy, C R, Ni, L, Wayne, S, O'Neill, M E, Van Camp, G, Coucke, P, Jain, P, Wilcox, E R, Smith, S D, Kenyon, J B, Zbar, R I, Smith, R J

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Complementary deoxyribonucleic acid cloning and characterization of a putative human axonemal dynein light chain gene von KASTURY, K, TAYLOR, W. E, SHEN, R, ARVER, S, GUTIERREZ, M, FISHER, C. E, COUCKE, P. J, VAN HAUWE, P, VAN CAMP, G, BHASIN, S

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