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... von Sampalis, J.S., Psaradellis, E., Pollock, C., Rickard, J., Rampakakis, E., Fonknechten, G., Toni, C., Lefay, D.

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

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

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

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A Fine Integrated Map of the SPG4 Locus Excludes an Expanded CAG Repeat in Chromosome 2p-Linked Autosomal Dominant Spastic Paraplegia von 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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Severe cystic fibrosis in a child homozygous for the G542 nonsense mutation in the CFTR gene von Bienvenu, T, Beldjord, C, Fonknechten, N, Kaplan, J C, Lenoir, G

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Identification of a new frameshift mutation (3724 delG) in exon 19 of the CFTR gene von Bienvenu, Thierry, Lenoir, Gérard, Fonknechten, Nuria, Desclaux-Arramond, François, Kaplan, Jean Claude, Beldjord, Cherif

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

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