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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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1999 | 1 |
2013 | 1 |
2020 | 1 |
2024 | 0 |
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Demystifying the management of hypertriglyceridaemia.
Nat Rev Cardiol. 2013 Nov;10(11):648-61. doi: 10.1038/nrcardio.2013.140. Epub 2013 Sep 24.
Nat Rev Cardiol. 2013.
PMID: 24060958
Review.
Extreme hypertriglyceridaemia requires strict dietary measures, and patients with a diagnosis of genetic lipoprotein lipase deficiency might benefit from LPL gene replacement therapy. Several therapies for regulating TRL metabolism, including inhibitor …
Extreme hypertriglyceridaemia requires strict dietary measures, and patients with a diagnosis of genetic lipoprotein lipase defici …
Persistent dyslipidemia in treatment of lysosomal acid lipase deficiency.
Pritchard AB, Strong A, Ficicioglu C.
Pritchard AB, et al.
Orphanet J Rare Dis. 2020 Feb 24;15(1):58. doi: 10.1186/s13023-020-1328-6.
Orphanet J Rare Dis. 2020.
PMID: 32093730
Free PMC article.
BACKGROUND: Lysosomal acid lipase deficiency (LALD) is an autosomal recessive inborn error of lipid metabolism characterized by impaired lysosomal hydrolysis and consequent accumulation of cholesteryl esters and triglycerides. The phenotypic spectrum is diverse, ran …
BACKGROUND: Lysosomal acid lipase deficiency (LALD) is an autosomal recessive inborn error of lipid metabolism characterized b …
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Atorvastatin in the management of an index patient with complete hepatic lipase deficiency.
Hegele RA, Little JA, Connelly PW.
Hegele RA, et al.
Atherosclerosis. 1999 Mar;143(1):219-22. doi: 10.1016/s0021-9150(98)00266-4.
Atherosclerosis. 1999.
PMID: 10208500
No abstract available.
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