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Expert Review of Clinical Pharmacology Volume 15, 2022 - Issue 4

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Safety and efficacy of therapies for chylomicronemia

Isabel ShamsudeenDepartment of Medicine, Schulich School of Medicine and Dentistry, Western University, London, Ontario, CanadaView further author information

Robert A. HegeleDepartment of Medicine, Schulich School of Medicine and Dentistry, Western University, London, Ontario, CanadaCorrespondence[email protected]

https://orcid.org/0000-0003-2861-5325 View further author information

Pages 395-405 | Received 08 May 2022, Accepted 21 Jun 2022, Published online: 03 Jul 2022

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https://doi.org/10.1080/17512433.2022.2094768
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Citations (7)

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Articles from other publishers (7)

Amanda J. Berberich & Robert A. Hegele. (2023) Genetic testing in dyslipidaemia: An approach based on clinical experience. Best Practice & Research Clinical Endocrinology & Metabolism 37:3, pages 101720.
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Amanda J. Berberich & Robert A. Hegele. (2023) The advantages and pitfalls of genetic analysis in the diagnosis and management of lipid disorders. Best Practice & Research Clinical Endocrinology & Metabolism 37:3, pages 101719.
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Shyann M.T. Hang, Robert A. Hegele & Amanda J. Berberich. (2023) Genetic determinants of pancreatitis: relevance in severe hypertriglyceridemia. Current Opinion in Lipidology 34:2, pages 59-69.
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Xavier Pintó, Marta Fanlo, Virginia Esteve, Jesús Millán, Agustín Blanco, Mariano Blasco, José Luís Díaz Díaz, Ángel Díaz Rodríguez, Alipio Mangas, Vicente Pascual, Juan Pedro Botet & Pablo Pérez Martínez. (2023) Colesterol remanente, riesgo vascular y prevención de la arteriosclerosis. Clínica e Investigación en Arteriosclerosis.
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Shehan D. Perera, Jian Wang, Adam D. McIntyre, Jacqueline S. Dron & Robert A. Hegele. (2023) The longitudinal triglyceride phenotype in heterozygotes with LPL pathogenic variants. Journal of Clinical Lipidology 17:1, pages 87-93.
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Robert A. Hegele. (2022) Is Genetic Testing in Hypertriglyceridemia Useful?. Arteriosclerosis, Thrombosis, and Vascular Biology 42:12, pages 1468-1470.
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Robert A Hegele. (2022) APOC3 Interference for Familial Chylomicronaemia Syndrome. European Endocrinology 18:2, pages 82.
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