Efficacy and long-term safety of alipogene tiparvovec (AAV1-LPLS447X) gene therapy for lipoprotein lipase deficiency: an open-label trial von Gaudet, D, Méthot, J, Déry, S, Brisson, D, Essiembre, C, Tremblay, G, Tremblay, K, de Wal, J, Twisk, J, van den Bulk, N, Sier-Ferreira, V, van Deventer, S

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The effect of spatial heterogenity on the aggregation of ticks on white-footed mice von DEVEVEY, G., BRISSON, D.

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Dissection of clinical and gene expression signatures of familial vs multifactorial chylomicronemia von Gaudet, D, Brisson, D, Tremblay, K

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Investigation of LPL independent pathways of TG-rich lipoprotein metabolism in LPL deficiency von Gaudet, D, Brisson, D, Tremblay, K

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DNA methylation variations at CETP and LPL gene promoter loci: New molecular biomarkers associated with blood lipid profile variability von Guay, S.P, Brisson, D, Lamarche, B, Marceau, P, Vohl, M.C, Gaudet, D, Bouchard, L

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Health supervision and anticipatory guidance in adult myotonic dystrophy type 1 von Gagnon, C, Chouinard, M.C, Laberge, L, Veillette, S, Bégin, P, Breton, R, Jean, S, Brisson, D, Gaudet, D, Mathieu, J

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Placental lipoprotein lipase DNA methylation levels are associated with gestational diabetes mellitus and maternal and cord blood lipid profiles von Houde, A. A., St-Pierre, J., Hivert, M. F., Baillargeon, J. P., Perron, P., Gaudet, D., Brisson, D., Bouchard, L.

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XRCC4 rs28360071 intronic variant is associated with increased risk for infant acute lymphoblastic leukemia with KMT2A rearrangements von Louzada-Neto, Orlando, Lopes, Bruno A, Brisson, Gisele D, Andrade, Francianne G, Cezar, Ingrid S, Santos-Rebouças, Cíntia B, Albano, Rodolpho M, Pombo-de-Oliveira, Maria S, Rossini, Ana

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Polymorphisms in protease-regulating genes are associated with recurrence of hospitalizations for acute abdominal pain in lipoprotein lipase deficiency von Tremblay, K, Dubois-Bouchard, C, Brisson, D, Gaudet, D

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Gene therapy for lipoprotein lipase deficiency (LPLD): Final results of 3 prospective gene therapy clinical studies and 1 retrospective clinical events analysis von Bernelot-Moens, S.J, Stroes, E.S, Carpentier, A.C, Brisson, D, Andersen, M, Meyer, C, Bruno, M, Gaudet, D

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Screening for non-alcoholic fatty liver disease using liver stiffness scores in patients with chylomicronemia von Maltais, M., Brisson, D., Gaudet, D.

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The g.-469G>A polymorphism in the GPIHBP1 gene promoter is associated with hypertriglyceridemia and has an additive effect on the risk conferred by LPL defective alleles von Guay, S.P, Gaudet, D, Brisson, D

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La francophonie de la Colombie-Britannique: Éducation, diversité, identités von Brisson, Geneviève, Léger, Rémi

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NUDT15 Polymorphism in Native American Populations of Brazil von Suarez‐Kurtz, Guilherme, Brisson, Gisele D., Hutz, Mara H., Petzl‐Erler, Maria Luiza, Salzano, Francisco M.

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Étude de la relation entre la personnalité et la performance à League of Legends chez les joueurs d’Amérique du Nord von D. Brisson, Francis

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Palmar striated xanthomas expression beyond type III dysbetalipoproteinemia von Roy, N., Brisson, D., Khoury, E., Gaudet, D.

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Lipoprotein lipase gene replacement therapy long-term effect on familial hyperchylomicronemia gene expression profile von Tremblay, K., Brisson, D., Gaudet, D.

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Comparison over 25 years of the burden of familial hypercholesterolemia on hospitalizations for coronary heart disease in a French-Canadian founder population von Lauziere, A, Brisson, D, Tremblay, G, Bedard, S, Khoury, E, Gaudet, D

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Post-prandial analysis of fluctuations in the platelet count and platelet activity in patients with the familial chylomicronemia syndrome von Larouche, M., Brisson, D., Khoury, E., Morissette, M.-C., Gaudet, D.

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Genetic susceptibility in childhood acute leukaemias: a systematic review von Brisson, Gisele D, Alves, Liliane R, Pombo-de-Oliveira, Maria S

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