Karine Tremblay
Karine Tremblay
Adresse e-mail validée de usherbrooke.ca
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Antisense inhibition of apolipoprotein C-III in patients with hypertriglyceridemia
D Gaudet, VJ Alexander, BF Baker, D Brisson, K Tremblay, W Singleton, ...
New England Journal of Medicine 373 (5), 438-447, 2015
Efficacy and long-term safety of alipogene tiparvovec (AAV1-LPL S447X) gene therapy for lipoprotein lipase deficiency: an open-label trial
D Gaudet, J Méthot, S Déry, D Brisson, C Essiembre, G Tremblay, ...
Gene therapy 20 (4), 361-369, 2013
Targeting APOC3 in the familial chylomicronemia syndrome
D Gaudet, D Brisson, K Tremblay, VJ Alexander, W Singleton, SG Hughes, ...
New England Journal of Medicine 371 (23), 2200-2206, 2014
Review of the clinical development of alipogene tiparvovec gene therapy for lipoprotein lipase deficiency
D Gaudet, J de Wal, K Tremblay, S Déry, S van Deventer, A Freidig, ...
Atherosclerosis Supplements 11 (1), 55-60, 2010
Replication of an association between 17q21 SNPs and asthma in a French-Canadian familial collection
AM Madore, K Tremblay, TJ Hudson, C Laprise
Human genetics 123 (1), 93-95, 2008
Effect of the DGAT1 inhibitor pradigastat on triglyceride and apoB48 levels in patients with familial chylomicronemia syndrome
CD Meyers, K Tremblay, A Amer, J Chen, L Jiang, D Gaudet
Lipids in health and disease 14 (1), 8, 2015
Long-term retrospective analysis of gene therapy with alipogene tiparvovec and its effect on lipoprotein lipase deficiency-induced pancreatitis
D Gaudet, ES Stroes, J Methot, D Brisson, K Tremblay, SJ Bernelot Moens, ...
Human gene therapy 27 (11), 916-925, 2016
Association of urokinase-type plasminogen activator with asthma and atopy
P Bégin, K Tremblay, D Daley, M Lemire, S Claveau, C Salesse, S Kacel, ...
American journal of respiratory and critical care medicine 175 (11), 1109-1116, 2007
Association study between the CX3CR1 gene and asthma
K Tremblay, M Lemire, V Provost, T Pastinen, Y Renaud, AJ Sandford, ...
Genes & Immunity 7 (8), 632-639, 2006
Etiology and risk of lactescent plasma and severe hypertriglyceridemia
K Tremblay, J Méthot, D Brisson, D Gaudet
Journal of clinical lipidology 5 (1), 37-44, 2011
Genes to diseases (G2D) computational method to identify asthma candidate genes
K Tremblay, M Lemire, C Potvin, A Tremblay, GM Hunninghake, BA Raby, ...
PloS one 3 (8), e2907, 2008
The DGAT1 inhibitor LCQ908 decreases triglyceride levels in patients with the familial chylomicronemia syndrome
C Meyers, D Gaudet, K Tremblay, A Amer, J Chen, F Aimin
Journal of Clinical Lipidology 6 (3), 266-267, 2012
A comparison of two sets of microarray experiments to define allergic asthma expression pattern
A Chamberland, AM Madore, K Tremblay, M Laviolette, C Laprise
Experimental lung research 35 (5), 399-410, 2009
Large-scale deletions of the ABCA1 gene in patients with hypoalphalipoproteinemia
JS Dron, J Wang, AJ Berberich, MA Iacocca, H Cao, P Yang, J Knoll, ...
Journal of lipid research 59 (8), 1529-1535, 2018
Comparison of the efficacy of fibrates on hypertriglyceridemic phenotypes with different genetic and clinical characteristics
D Brisson, J Méthot, K Tremblay, M Tremblay, P Perron, D Gaudet
Pharmacogenetics and genomics 20 (12), 742-747, 2010
Genetic variation in immune signaling genes differentially expressed in asthmatic lung tissues
K Tremblay, D Daley, A Chamberland, M Lemire, A Montpetit, M Laviolette, ...
Journal of allergy and clinical immunology 122 (3), 529-536. e17, 2008
Association of CTRC and SPINK1 gene variants with recurrent hospitalizations for pancreatitis or acute abdominal pain in lipoprotein lipase deficiency
K Tremblay, C Dubois-Bouchard, D Brisson, D Gaudet
Frontiers in genetics 5, 90, 2014
Medical resource use and costs associated with chylomicronemia
D Gaudet, J Signorovitch, E Swallow, L Fan, K Tremblay, D Brisson, ...
Journal of Medical Economics 16 (5), 657-666, 2013
Pharmacogenetic testing in primary care practice: opinions of physicians, pharmacists and patients
MP Frigon, MÈ Blackburn, C Dubois-Bouchard, AL Gagnon, S Tardif, ...
Pharmacogenomics 20 (8), 589-598, 2019
Natural history (up to 15 years) of platelet count in 84 patients with familial hyperchylomicronemia due to lipoprotein lipase deficiency
D Gaudet, A Baass, K Tremblay, D Brisson, N Laflamme, M Paquette, ...
Journal of Clinical Lipidology 11 (3), 797-798, 2017
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