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Related Articles by Review for PMID: 32809630

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Page 1
Lipoprotein Lipase Deficiency.
Balasubramanian S, Aggarwal P, Sharma S. Balasubramanian S, et al. 2024 Dec 10. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–. 2024 Dec 10. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–. PMID: 32809630 Free Books & Documents.
The role of registries in rare genetic lipid disorders: Review and introduction of the first global registry in lipoprotein lipase deficiency.
Steinhagen-Thiessen E, Stroes E, Soran H, Johnson C, Moulin P, Iotti G, Zibellini M, Ossenkoppele B, Dippel M, Averna MR; GENIALL Investigators. Steinhagen-Thiessen E, et al. Atherosclerosis. 2017 Jul;262:146-153. doi: 10.1016/j.atherosclerosis.2016.08.023. Epub 2016 Aug 21. Atherosclerosis. 2017. PMID: 28284702 Review.
[Chylomicronemia syndrome].
Francis A, Levy Y. Francis A, et al. Harefuah. 2002 Feb;141(2):201-3, 221, 220. Harefuah. 2002. PMID: 11905095 Review. Hebrew.
The familial chylomicronemia syndrome.
Santamarina-Fojo S. Santamarina-Fojo S. Endocrinol Metab Clin North Am. 1998 Sep;27(3):551-67, viii. doi: 10.1016/s0889-8529(05)70025-6. Endocrinol Metab Clin North Am. 1998. PMID: 9785052 Review.
21 results