Molecular diagnosis of autosomal dominant early onset Alzheimer’s disease: an update von Raux, G, Guyant-Maréchal, L, Martin, C, Bou, J, Penet, C, Brice, A, Hannequin, D, Frebourg, T, Campion, D

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Variations in the APP gene promoter region and risk of Alzheimer disease von GUYANT-MARECHAL, L, ROVELET-LECRUX, A, DELEUZE, J.-F, FREBOURG, T, BRICE, A, LAMBERT, J.-C, CAMPION, D, GOUMIDI, L, COUSIN, E, HANNEQUIN, D, RAUX, G, PENET, C, RICARD, S, MACE, S, AMOUYEL, P

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Hyperprolinemia is a risk factor for schizoaffective disorder von Jacquet, H, Demily, C, Houy, E, Hecketsweiler, B, Bou, J, Raux, G, Lerond, J, Allio, G, Haouzir, S, Tillaux, A, Bellegou, C, Fouldrin, G, Delamillieure, P, Ménard, J F, Dollfus, S, D'Amato, T, Petit, M, Thibaut, F, Frébourg, T, Campion, D

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Dementia with prominent frontotemporal features associated with L113P presenilin 1 mutation von RAUX, G, GANTIER, R, THOMAS-ANTERION, C, BOULLIAT, J, VERPILLAT, P, HANNEQUIN, D, BRICE, A, FREBOURG, T, CAMPION, D

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The promoter −194 C polymorphism of the nicotinic alpha 7 receptor gene has a protective effect against the P50 sensory gating deficit von Houy, E, Raux, G, Thibaut, F, Belmont, A, Demily, C, Allio, G, Haouzir, S, Fouldrin, G, Petit, M, Frebourg, T, Campion, D

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The -2 bp deletion in exon 6 of the 'alpha 7-like' nicotinic receptor subunit gene is a risk factor for the P50 sensory gating deficit von RAUX, G, BONNET-BRILHAULT, F, FREBOURG, T, THIBAUT, F, CAMPION, D, LOUCHART, S, HOUY, E, GANTIER, R, LEVILLAIN, D, ALLIO, G, HAOUZIR, S, PETIT, M, MARTINEZ, M

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APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy von Rovelet-Lecrux, Anne, Hannequin, Didier, Raux, Gregory, Meur, Nathalie Le, Laquerrière, Annie, Vital, Anne, Dumanchin, Cécile, Feuillette, Sébastien, Brice, Alexis, Vercelletto, Martine, Dubas, Frédéric, Frebourg, Thierry, Campion, Dominique

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Comparison of a quantitative PCR method with FISH for the assessment of the four aneuploidies commonly evaluated in CLL patients von BASTARD, C, RAUX, G, FREBOURG, T, TILLY, H, FRUCHART, C, PARMENTIER, F, VAUR, D, PENTHER, D, TROUSSARD, X, NAGIB, D, LEPRETRE, S, TOSI, M

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Very early onset AD with a de novo mutation in the presenilin 1 gene (Met 233 Leu) von PORTET, F, DAUVILLIERS, Y, CAMPION, D, RAUX, G, HAUW, J. J, LYON-CAEN, O, CAMU, W, TOUCHON, J

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The severe form of type I hyperprolinaemia results from homozygous inactivation of the PRODH gene von Jacquet, H, Berthelot, J, Bonnemains, C, Simard, G, Saugier-Veber, P, Raux, G, Campion, D, Bonneau, D, Frebourg, T

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73. Can tear staining and skin lesions be used to assess pig welfare? von Dupuis, A., Fablet, C., Eono, F., Eveno, É., Poulain, G., Raux, G., Simon, G., Rose, N., Parois, S.

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Early-Onset Autosomal Dominant Alzheimer Disease: Prevalence, Genetic Heterogeneity, and Mutation Spectrum von Campion, Dominique, Dumanchin, Cécile, Hannequin, Didier, Dubois, Bruno, Belliard, Serge, Puel, Michèle, Thomas-Anterion, Catherine, Michon, Agnès, Martin, Cosette, Charbonnier, Françoise, Raux, Grégory, Camuzat, Agnès, Penet, Christiane, Mesnage, Valérie, Martinez, Maria, Clerget-Darpoux, Françoise, Brice, Alexis, Frebourg, Thierry

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PRODH mutations and hyperprolinemia in a subset of schizophrenic patients von Jacquet, Hélène, Raux, Grégory, Thibaut, Florence, Hecketsweiler, Bernadette, Houy, Emmanuelle, Demilly, Caroline, Haouzir, Sadeq, Allio, Gabrielle, Fouldrin, Gael, Drouin, Valérie, Bou, Jacqueline, Petit, Michel, Campion, Dominique, Frébourg, Thierry

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Bilateral hypoglossal nerve stimulation for treatment of obstructive sleep apnea von Eastwood, P., Barnes, M., Mackay, S., Wheatley, J., Hillman, D., Nguyen, X.-L., Lewis, R., Campbell, M., Petelle, B., Walsh, J., Jones, A., Palme, C., Bizon, A., Meslier, N., Bertolus, C., Maddison, K., Laccourreye, L., Raux, G., Denoncin, K., Attali, V., Gagnadoux, F., Launois, S.

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A novel presenilin 1 missense mutation (L153V) segregating with early-onset autosomal dominant Alzheimer's disease von Raux, G., Gantier, R., Martin, C., Pothin, Y., Brice, A., Frebourg, T., Campion, D.

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A polymorphic variant of the gene coding desmoglein 1, the target autoantigen of pemphigus foliaceus, is associated with the disease von MARTEL, P, GILBERT, D, DROUOT, L, PROST, C, RAUX, G, DELAPORTE, E, TOLY, P, TRON, F

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Detection of exon deletions and duplications of the mismatch repair genes in hereditary nonpolyposis colorectal cancer families using multiplex polymerase chain reaction of short f... von CHARBONNIER, F, RAUX, G, QING WANG, DROUOT, N, CORDIER, F, LIMACHER, J.-M, SAURIN, J.-C, PUISIEUX, A, OLSCHWANG, S, FREBOURG, T

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Screening for TP53 rearrangements in families with the Li–Fraumeni syndrome reveals a complete deletion of the TP53 gene von Bougeard, Gaëlle, Brugières, Laurence, Chompret, Agnès, Gesta, Paul, Charbonnier, Françoise, Valent, Alexander, Martin, Cosette, Raux, Grégory, Feunteun, Jean, Paillerets, Brigitte Bressac-de, Frébourg, Thierry

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Pemphigus is not associated with allotypic markers of immunoglobulin kappa von Zitouni, M, Martel, P, Ben Ayed, M, Raux, G, Gilbert, D, Joly, P, Mokhtar, I, Ridha Kamoun, M, Turki, H, Zahaf, A, Mokni, M, Ben Osman, A, Masmoudi, H, Makni, S, Tron, F

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Comparison of Structural Characteristics of Antisubnucleosome and Anti-DNA Monoclonal Antibodies Derived from Lupus Mice von KOUTOUZOV, S., JOVELIN, F., BRARD, F., RAUX, G., TRON, F., GILBERT, D.

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