Search Results - Fonknechten, G

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  1. 1
    P759Post-hoc analysis of Confidence II, Protect I, Shake the habit I and Shake the habit II studies in mild to moderate hypertensive patients treated with perindopril and atorvastatin concomitantly

    P759Post-hoc analysis of Confidence II, Protect I, Shake the habit I and Shake the habit II studies in mild to moderate hypertensive patients treated with perindopril and atorvasta... by Sampalis, J.S., Psaradellis, E., Pollock, C., Rickard, J., Rampakakis, E., Fonknechten, G., Toni, C., Lefay, D.

    Published in European heart journal
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  2. 2
    Synthesis and characterisation of dimers of catechin and epicatechin

    Synthesis and characterisation of dimers of catechin and epicatechin by Fonknechten, G, Moll, M, Cagniant, D, Kirsch, G, Muller, J.F

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  3. 3
    Unique features revealed by the genome sequence of Acinetobacter sp. ADP1, a versatile and naturally transformation competent bacterium

    Unique features revealed by the genome sequence of Acinetobacter sp. ADP1, a versatile and naturally transformation competent bacterium by Barbe, Valérie, Vallenet, David, Fonknechten, Nuria, Kreimeyer, Annett, Oztas, Sophie, Labarre, Laurent, Cruveiller, Stéphane, Robert, Catherine, Duprat, Simone, Wincker, Patrick, Ornston, L. Nicholas, Weissenbach, Jean, Marlière, Philippe, Cohen, Georges N., Médigue, Claudine

    Published in Nucleic acids research
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  4. 4
    Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3A

    Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3A by ABEL, Annette, FONKNECHTEN, Nuria, HAZAN, Jamilé, HOFER, Anne, DÜRR, Alexandra, CRUAUD, Corinne, VOIT, Thomas, WEISSENBACH, Jean, BRICE, Alexis, KLIMPE, Sven, AUBURGER, Georg

    Published in Neurogenetics
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  5. 5
    A Fine Integrated Map of the SPG4 Locus Excludes an Expanded CAG Repeat in Chromosome 2p-Linked Autosomal Dominant Spastic Paraplegia

    A Fine Integrated Map of the SPG4 Locus Excludes an Expanded CAG Repeat in Chromosome 2p-Linked Autosomal Dominant Spastic Paraplegia by Hazan, Jamilé, Davoine, Claire-Sophie, Mavel, Delphine, Fonknechten, Nùria, Paternotte, Caroline, Fizames, Cécile, Cruaud, Corinne, Samson, Delphine, Muselet, Delphine, Vega-Czarny, Nathalie, Brice, Alexis, Gyapay, Gabor, Heilig, Roland, Fontaine, Bertrand, Weissenbach, Jean

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  6. 6
    Severe cystic fibrosis in a child homozygous for the G542 nonsense mutation in the CFTR gene

    Severe cystic fibrosis in a child homozygous for the G542 nonsense mutation in the CFTR gene by Bienvenu, T, Beldjord, C, Fonknechten, N, Kaplan, J C, Lenoir, G

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  7. 7
    Severe cystic fibrosis in a child homozygous for the G542 nonsense mutation in the CFTR gene

    Severe cystic fibrosis in a child homozygous for the G542 nonsense mutation in the CFTR gene by Bienvenu, T, Beldjord, C, Fonknechten, N, Kaplan, J C, Lenoir, G

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