Search Results - Bonneau, Esther

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  1. 1
    Patterns of paralytic shellfish toxicity in the St. Lawrence region in relationship with the abundance and distribution of Alexandrium tamarense

    Patterns of paralytic shellfish toxicity in the St. Lawrence region in relationship with the abundance and distribution of Alexandrium tamarense by Blasco, Dolors, Levasseur, Maurice, Bonneau, Esther, Gelinas, Roger, Packard, T. T.

    Published in Scientia marina
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  2. 2
    The link between precipitation, river runoff, and blooms of the toxic dinoflagellate Alexandrium tamarense in the St. Lawrence

    The link between precipitation, river runoff, and blooms of the toxic dinoflagellate Alexandrium tamarense in the St. Lawrence by Weise, Andréa M, Levasseur, Maurice, Saucier, François J, Senneville, Simon, Bonneau, Esther, Roy, Suzanne, Sauvé, Gilbert, Michaud, Sonia, Fauchot, Juliette

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  3. 3
    OPA1 mutations induce mitochondrial DNA instability and optic atrophy ‘plus’ phenotypes

    OPA1 mutations induce mitochondrial DNA instability and optic atrophy ‘plus’ phenotypes by Amati-Bonneau, Patrizia, Valentino, Maria Lucia, Reynier, Pascal, Gallardo, Maria Esther, Bornstein, Belén, Boissière, Anne, Campos, Yolanda, Rivera, Henry, de la Aleja, Jesús González, Carroccia, Rosanna, Iommarini, Luisa, Labauge, Pierre, Figarella-Branger, Dominique, Marcorelles, Pascale, Furby, Alain, Beauvais, Katell, Letournel, Franck, Liguori, Rocco, La Morgia, Chiara, Montagna, Pasquale, Liguori, Maria, Zanna, Claudia, Rugolo, Michela, Cossarizza, Andrea, Wissinger, Bernd, Verny, Christophe, Schwarzenbacher, Robert, Martín, Miguel Ángel, Arenas, Joaquιn, Ayuso, Carmen, Garesse, Rafael, Lenaers, Guy, Bonneau, Dominique, Carelli, Valerio

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  4. 4
    Solubility survey of fragments of the neurofibromatosis type 1 protein neurofibromin

    Solubility survey of fragments of the neurofibromatosis type 1 protein neurofibromin by Bonneau, Fabien, Lenherr, Esther D., Pena, Vladimir, Hart, Darren J., Scheffzek, Klaus

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  5. 5
    OPAI mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes. Commentary

    OPAI mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes. Commentary by ZEVIANI, Massimo, AMATI-BONNEAU, Patrizia, CARROCCIA, Rosanna, LOMMARINI, Luisa, LABAUGE, Pierre, FIGARELLA-BRANGER, Dominique, MARCORELLES, Pascale, FURBY, Alain, BEAUVAIS, Katell, LETOURNEL, Franck, LIGUORI, Rocco, LA MORGIA, Chiara, VALENTINO, Maria Lucia, MONTAGNA, Pasquale, LIGUORI, Maria, ZANNA, Claudia, RUGOLO, Michela, COSSARIZZA, Andrea, WISSINGER, Bernd, VERNY, Christophe, SCHWARZENBACHER, Robert, MARTIA, Miguel Ngel, ARENAS, Joaquin, REYNIER, Pascal, AYUSO, Carmen, GARESSE, Rafael, LENAERS, Guy, BONNEAU, Dominique, CARELLI, Valerio, GALLARDO, Maria Esther, BORNSTEIN, Belén, BOISSIERE, Anne, CAMPOS, Yolanda, RIVERA, Henry, DE LA ALEJA, Jesus Gonzalez

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  6. 6
    No evidence of genetic heterogeneity in dominant optic atrophy

    No evidence of genetic heterogeneity in dominant optic atrophy by Bonneau, D, Souied, E, Gerber, S, Rozet, J M, D'Haens, E, Journel, H, Plessis, G, Weissenbach, J, Munnich, A, Kaplan, J

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