Familial chylomicronemia syndrome: an under‐recognized cause of severe hypertriglyceridaemia von Baass, A., Paquette, M., Bernard, S., Hegele, R.A.

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Ambroxol as a novel disease-modifying treatment for Parkinson's disease dementia: protocol for a single-centre, randomized, double-blind, placebo-controlled trial von Silveira, C R A, MacKinley, J, Coleman, K, Li, Z, Finger, E, Bartha, R, Morrow, S A, Wells, J, Borrie, M, Tirona, R G, Rupar, C A, Zou, G, Hegele, R A, Mahuran, D, MacDonald, P, Jenkins, M E, Jog, M, Pasternak, S H

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Conservative management in hypertriglyceridemia‐associated pancreatitis von Berberich, A. J., Ziada, A., Zou, G. Y., Hegele, R. A.

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Gas production and transport during bench-scale electrical resistance heating of water and trichloroethene von Hegele, P.R., Mumford, K.G.

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Pharmacogenomics, Lipid Disorders, and Treatment Options von Gryn, S E, Hegele, R A

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Nuclear lamin A/C R482Q mutation in Canadian kindreds with Dunnigan-type familial partial lipodystrophy von HENIAN CAO, HEGELE, R. A

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Mutations in LPL, APOC2, APOA5, GPIHBP1 and LMF1 in patients with severe hypertriglyceridaemia von Surendran, R. P., Visser, M. E., Heemelaar, S., Wang, J., Peter, J., Defesche, J. C., Kuivenhoven, J. A., Hosseini, M., Péterfy, M., Kastelein, J. J. P., Johansen, C. T., Hegele, R. A., Stroes, E. S. G., Dallinga-Thie, G. M.

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Evaluation of apolipoprotein A5 variants: A cohort of patients with severe hypertriglyceridemia from Turkiye von Cakmak, B., Yeral, S., Ozcan, B., Pariltay, E., Ozgul, S., Simsir, I.Y., Hegele, R.A.

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Vascular Calcifications in Homozygote Familial Hypercholesterolemia von Awan, Z, Alrasadi, K, Francis, G A, Hegele, R A, McPherson, R, Frohlich, J, Valenti, D, de Varennes, B, Marcil, M, Gagne, C, Genest, J, Couture, P

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The lipid-lowering effects of lomitapide are unaffected by adjunctive apheresis in patients with homozygous familial hypercholesterolaemia – A post-hoc analysis of a Phase 3, singl... von Stefanutti, C, Blom, D.J, Averna, M.R, Meagher, E.A, Theron, H. dT, Marais, A.D, Hegele, R.A, Sirtori, C.R, Shah, P.K, Gaudet, D, Vigna, G.B, Sachais, B.S, Di Giacomo, S, du Plessis, A.M.E, Bloedon, L.T, Balser, J, Rader, D.J, Cuchel, M

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Differences in risk factors, atherosclerosis, and cardiovascular disease between ethnic groups in Canada: the Study of Health Assessment and Risk in Ethnic groups (SHARE) von Anand, Sonia S, Yusuf, Salim, Vuksan, Vladmir, Devanesen, Sudarshan, Teo, Koon K, Montague, Patricia A, Kelemen, Linda, Yi, Cheelong, Lonn, Eva, Gerstein, Hertzel, Hegele, Robert A, McQueen, Matthew

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Novel lamin A/C gene (LMNA) mutations in atypical progeroid syndromes von Csoka, A B, Cao, H, Sammak, P J, Constantinescu, D, Schatten, G P, Hegele, R A

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Hutchinson-Gilford progeria syndrome von Pollex, RL, Hegele, RA

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Using Mendelian randomization to determine causative factors in cardiovascular disease von Johansen, C. T., Hegele, R. A.

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Lessons from human mutations in PPARγ von Hegele, R A

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LMNA mutation position predicts organ system involvement in laminopathies von Hegele, RA

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Respiratory syncytial virus therapy and prophylaxis: have we finally turned the corner? von Hegele, R G

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Depression, marijuana use and early-onset marijuana use conferred unique effects on neural connectivity and cognition von Osuch, E. A., Manning, K., Hegele, R. A., Théberge, J., Neufeld, R., Mitchell, D., Williamson, P., Gardner, R. C.

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Characterization of the I4399M variant of apolipoprotein(a): implications for altered prothrombotic properties of lipoprotein(a) von Scipione, C. A., McAiney, J. T., Simard, D. J., Bazzi, Z. A., Gemin, M., Romagnuolo, R., Macrae, F. L., Ariëns, R. A., Hegele, R. A., Auld, J., Gauld, J. W., Boffa, M. B., Koschinsky, M. L.

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Biallelic mutations at PPARG cause a congenital, generalized lipodystrophy similar to the Berardinelli–Seip syndrome von Dyment, D.A, Gibson, W.T, Huang, L, Bassyouni, H, Hegele, R.A, Innes, A.M

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