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Volanesorsen to Prevent Acute Pancreatitis in Hypertriglyceridemia.
Alexander VJ, Karwatowska-Prokopczuk E, Prohaska TA, Li L, Geary RS, Gouni-Berthold I, Oral EA, Hegele RA, Stroes ESG, Witztum JL, Tsimikas S. Alexander VJ, et al. Among authors: hegele ra. N Engl J Med. 2024 Feb 1;390(5):476-477. doi: 10.1056/NEJMc2306575. N Engl J Med. 2024. PMID: 38294982 No abstract available.
Inherited lipodystrophies and the metabolic syndrome.
Monajemi H, Stroes E, Hegele RA, Fliers E. Monajemi H, et al. Among authors: hegele ra. Clin Endocrinol (Oxf). 2007 Oct;67(4):479-84. doi: 10.1111/j.1365-2265.2007.02906.x. Epub 2007 Jun 11. Clin Endocrinol (Oxf). 2007. PMID: 17561981 Review.
Mutations in LPL, APOC2, APOA5, GPIHBP1 and LMF1 in patients with severe hypertriglyceridaemia.
Surendran RP, Visser ME, Heemelaar S, Wang J, Peter J, Defesche JC, Kuivenhoven JA, Hosseini M, Péterfy M, Kastelein JJ, Johansen CT, Hegele RA, Stroes ES, Dallinga-Thie GM. Surendran RP, et al. Among authors: hegele ra. J Intern Med. 2012 Aug;272(2):185-96. doi: 10.1111/j.1365-2796.2012.02516.x. Epub 2012 Feb 13. J Intern Med. 2012. PMID: 22239554 Free PMC article.
Hypertriglyceridemia.
Brahm A, Hegele RA. Brahm A, et al. Among authors: hegele ra. Nutrients. 2013 Mar 22;5(3):981-1001. doi: 10.3390/nu5030981. Nutrients. 2013. PMID: 23525082 Free PMC article.
The polygenic nature of hypertriglyceridaemia: implications for definition, diagnosis, and management.
Hegele RA, Ginsberg HN, Chapman MJ, Nordestgaard BG, Kuivenhoven JA, Averna M, Borén J, Bruckert E, Catapano AL, Descamps OS, Hovingh GK, Humphries SE, Kovanen PT, Masana L, Pajukanta P, Parhofer KG, Raal FJ, Ray KK, Santos RD, Stalenhoef AF, Stroes E, Taskinen MR, Tybjærg-Hansen A, Watts GF, Wiklund O; European Atherosclerosis Society Consensus Panel. Hegele RA, et al. Lancet Diabetes Endocrinol. 2014 Aug;2(8):655-66. doi: 10.1016/S2213-8587(13)70191-8. Epub 2013 Dec 23. Lancet Diabetes Endocrinol. 2014. PMID: 24731657 Free PMC article. Review.
A Novel Generalized Lipodystrophy-Associated Progeroid Syndrome Due to Recurrent Heterozygous LMNA p.T10I Mutation.
Hussain I, Patni N, Ueda M, Sorkina E, Valerio CM, Cochran E, Brown RJ, Peeden J, Tikhonovich Y, Tiulpakov A, Stender SRS, Klouda E, Tayeh MK, Innis JW, Meyer A, Lal P, Godoy-Matos AF, Teles MG, Adams-Huet B, Rader DJ, Hegele RA, Oral EA, Garg A. Hussain I, et al. Among authors: hegele ra. J Clin Endocrinol Metab. 2018 Mar 1;103(3):1005-1014. doi: 10.1210/jc.2017-02078. J Clin Endocrinol Metab. 2018. PMID: 29267953 Free PMC article.
Large-scale deletions of the ABCA1 gene in patients with hypoalphalipoproteinemia.
Dron JS, Wang J, Berberich AJ, Iacocca MA, Cao H, Yang P, Knoll J, Tremblay K, Brisson D, Netzer C, Gouni-Berthold I, Gaudet D, Hegele RA. Dron JS, et al. Among authors: hegele ra. J Lipid Res. 2018 Aug;59(8):1529-1535. doi: 10.1194/jlr.P086280. Epub 2018 Jun 4. J Lipid Res. 2018. PMID: 29866657 Free PMC article.
Lipid-Lowering Agents.
Hegele RA, Tsimikas S. Hegele RA, et al. Circ Res. 2019 Feb;124(3):386-404. doi: 10.1161/CIRCRESAHA.118.313171. Circ Res. 2019. PMID: 30702996
Differentiating Familial Chylomicronemia Syndrome From Multifactorial Severe Hypertriglyceridemia by Clinical Profiles.
O'Dea LSL, MacDougall J, Alexander VJ, Digenio A, Hubbard B, Arca M, Moriarty PM, Kastelein JJP, Bruckert E, Soran H, Witztum JL, Hegele RA, Gaudet D. O'Dea LSL, et al. Among authors: hegele ra. J Endocr Soc. 2019 Oct 11;3(12):2397-2410. doi: 10.1210/js.2019-00214. eCollection 2019 Dec 1. J Endocr Soc. 2019. PMID: 31777768 Free PMC article.
934 results