Search Results - Divry, V

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  1. 1
    Drying Mechanisms in Plasticized Latex Films: Role of Horizontal Drying Fronts

    Drying Mechanisms in Plasticized Latex Films: Role of Horizontal Drying Fronts by Divry, V, Gromer, A, Nassar, M, Lambour, C, Collin, D, Holl, Y

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  2. 2
    Influence of formulation on friction properties of latex films

    Influence of formulation on friction properties of latex films by Divry, V., Jacomine, L., Le Houérou, V., Collin, D., Gauthier, C., Holl, Y.

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  3. 3
    Additive effect of APOE rare variants on the phenotype of familial hypercholesterolemia

    Additive effect of APOE rare variants on the phenotype of familial hypercholesterolemia by Marmontel, O., Khalil, Y. Abou, Bluteau, O., Cariou, B., Carreau, V., Charrière, S., Divry, E., Moulin, P., Peretti, N., Rabès, J.-P., Varret, M., Carrié, A., Di Filippo, M.

    Published in Atherosclerosis
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  4. 4
    Combined liver-kidney transplantation in primary hyperoxaluria type 1

    Combined liver-kidney transplantation in primary hyperoxaluria type 1 by Cochat, P, Gaulier, J M, Koch Nogueira, P C, Feber, J, Jamieson, N V, Rolland, M O, Divry, P, Bozon, D, Dubourg, L

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  5. 5
    Identification of a Mutation Cluster in Mevalonate Kinase Deficiency, Including a New Mutation in a Patient of Mennonite Ancestry

    Identification of a Mutation Cluster in Mevalonate Kinase Deficiency, Including a New Mutation in a Patient of Mennonite Ancestry by Hinson, Debra D., Ross, Richard M., Krisans, Skaidrite, Shaw, Joanne L., Kozich, Viktor, Rolland, Marie-Odile, Divry, Priscille, Mancini, Josette, Hoffmann, Georg F., Gibson, K. Michael

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  6. 6
    N-acetylaspartylglutamate in Canavan disease : an adverse effector?

    N-acetylaspartylglutamate in Canavan disease : an adverse effector? by BURLINA, A. P, FERRARI, V, DIVRY, P, GRADOWSKA, W, JAKOBS, C, BENNETT, M. J, SEWELL, A. C, DIONISI-VICI, C, BURLINA, A. B

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  7. 7
    A rare disease-associated mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene changes a conserved arginine, previously shown to be functionally essential in short-chain acyl-CoA dehydrogenase (SCAD)

    A rare disease-associated mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene changes a conserved arginine, previously shown to be functionally essential in short-chain... by ANDRESEN, B. S, BROSS, P, CURTIS, D, DIVRY, P, VIANEY-SABAN, C, GREGERSEN, N, JENSEN, T. G, WINTER, V, KNUDSEN, I, KØLVRAA, S, JENSEN, U. B, BOLUND, L, DURAN, M, JUNG-JA KIM

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  8. 8
    The most common mutation causing medium-chain acyl-CoA dehydrogenase deficiency is strongly associated with a particular haplotype in the region of the gene

    The most common mutation causing medium-chain acyl-CoA dehydrogenase deficiency is strongly associated with a particular haplotype in the region of the gene by KOLVRAA, S, GREGERSEN, N, BOLUND, L, BLAKEMORE, A. I. F, SCHNEIDERMANN, A. K, WINTER, V, ANDRESEN, B. S, CURTIS, D, ENGEL, P. C, PRICILLE, D, RHEAD, W

    Published in Human genetics
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  9. 9
    UNE MALADIE FAMILIALE CARACTÉRISÉE PAR UNE ANGIOMATOSE DIFFUSE CORTICO-MÉNINGÉE NON CALCIFIANTE ET UNE DÉMYÉLINISATION PROGRESSIVE DE LA SUBSTANCE BLANCHE

    UNE MALADIE FAMILIALE CARACTÉRISÉE PAR UNE ANGIOMATOSE DIFFUSE CORTICO-MÉNINGÉE NON CALCIFIANTE ET UNE DÉMYÉLINISATION PROGRESSIVE DE LA SUBSTANCE BLANCHE by Divry (Liège), Paul, Bogaert (Anvers), Ludo Van

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