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1976
2025

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Year Number of Results
1976 1
1992 1
1996 2
1997 2
1998 1
1999 1
2000 1
2001 6
2002 1
2003 12
2004 6
2005 6
2006 5
2007 6
2008 5
2009 4
2010 3
2011 5
2013 4
2014 7
2015 3
2017 2
2018 4
2019 7
2020 4
2021 6
2022 4
2023 2
2025 0

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99 results

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Page 1
ABC Family Transporters.
Liu X. Liu X. Adv Exp Med Biol. 2019;1141:13-100. doi: 10.1007/978-981-13-7647-4_2. Adv Exp Med Biol. 2019. PMID: 31571164 Review.
Several human diseases such as cystic fibrosis, sitosterolemia, Tangier disease, intrahepatic cholestasis, and retinal degeneration are associated with mutations in corresponding transporters. ...
Several human diseases such as cystic fibrosis, sitosterolemia, Tangier disease, intrahepatic cholestasis, and retinal degeneration a …
Familial Hypercholesterolemia: The Most Frequent Cholesterol Metabolism Disorder Caused Disease.
Benito-Vicente A, Uribe KB, Jebari S, Galicia-Garcia U, Ostolaza H, Martin C. Benito-Vicente A, et al. Int J Mol Sci. 2018 Nov 1;19(11):3426. doi: 10.3390/ijms19113426. Int J Mol Sci. 2018. PMID: 30388787 Free PMC article. Review.
Malfunctioning of cholesterol metabolism is caused by multiple hereditary diseases, including Familial Hypercholesterolemia, Sitosterolemia Type C and Niemann-Pick Type C1. Of these, familial hypercholesterolemia (FH) is a common inherited autosomal co-dominant disorder ch …
Malfunctioning of cholesterol metabolism is caused by multiple hereditary diseases, including Familial Hypercholesterolemia, Sitosterolem
The Inherited Hypercholesterolemias.
Loh WJ, Watts GF. Loh WJ, et al. Endocrinol Metab Clin North Am. 2022 Sep;51(3):511-537. doi: 10.1016/j.ecl.2022.02.006. Epub 2022 Jul 4. Endocrinol Metab Clin North Am. 2022. PMID: 35963626 Review.
In this review, we discuss familial hypercholesterolemia (FH), FH-mimics (eg, polygenic hypercholesterolemia [PH], FCH, sitosterolemia), and other inherited forms of hypercholesterolemia (eg, hyper-lipoprotein(a) levels [hyper-Lp(a)]). ...
In this review, we discuss familial hypercholesterolemia (FH), FH-mimics (eg, polygenic hypercholesterolemia [PH], FCH, sitosterolemia
Update on Sitosterolemia and Atherosclerosis.
Rocha VZ, Tada MT, Chacra APM, Miname MH, Mizuta MH. Rocha VZ, et al. Curr Atheroscler Rep. 2023 May;25(5):181-187. doi: 10.1007/s11883-023-01092-4. Epub 2023 Mar 10. Curr Atheroscler Rep. 2023. PMID: 36897412 Review.
PURPOSE OF REVIEW: The purpose of this review was to summarize important and updated information on sitosterolemia. Sitosterolemia is an inherited lipid disorder consisting of high levels of plasma plant sterols. ...RECENT FINDINGS: Since hypercholesterolemia is oft …
PURPOSE OF REVIEW: The purpose of this review was to summarize important and updated information on sitosterolemia. Sitosterolemia
[Sitosterolemia (phytosterolemia)].
Lütjohann D. Lütjohann D. Internist (Berl). 2019 Aug;60(8):871-877. doi: 10.1007/s00108-019-0635-2. Internist (Berl). 2019. PMID: 31254003 Review. German.
Sitosterolemia or phytosterolemia is a rare autosomal recessive hereditary lipid storage disorder. ...Phytosterols are found mainly in vegetable oils, margarine, nuts, grains, soybeans and avocados. Patients with sitosterolemia show extreme phenotypic heterogeneity
Sitosterolemia or phytosterolemia is a rare autosomal recessive hereditary lipid storage disorder. ...Phytosterols are found mainly i
Sitosterolemia.
Salen G, Shefer S, Nguyen L, Ness GC, Tint GS, Shore V. Salen G, et al. J Lipid Res. 1992 Jul;33(7):945-55. J Lipid Res. 1992. PMID: 1431587 Free article. Review.
Sitosterolemia is a rare inherited lipid storage disease characterized chemically by the accumulation of plant sterols and 5 alpha-saturated stanols in plasma and tissues. ...
Sitosterolemia is a rare inherited lipid storage disease characterized chemically by the accumulation of plant sterols and 5 alpha-sa
Sitosterolemia.
Salen G, Patel S, Batta AK. Salen G, et al. Cardiovasc Drug Rev. 2002 Winter;20(4):255-70. doi: 10.1111/j.1527-3466.2002.tb00096.x. Cardiovasc Drug Rev. 2002. PMID: 12481199 Review.
Sitosterolemia was first described 28 years ago in two sisters. They had tendonxanthomas, normal plasma cholesterol levels, and elevated plant sterol levels. ...Bile acid binding resins and ileal bypass surgery are effective treatments for sitosterolemic patients, whereas
Sitosterolemia was first described 28 years ago in two sisters. They had tendonxanthomas, normal plasma cholesterol levels, and eleva
Diagnosis and Management of Sitosterolemia 2021.
Tada H, Nomura A, Ogura M, Ikewaki K, Ishigaki Y, Inagaki K, Tsukamoto K, Dobashi K, Nakamura K, Hori M, Matsuki K, Yamashita S, Yokoyama S, Kawashiri MA, Harada-Shiba M. Tada H, et al. J Atheroscler Thromb. 2021 Aug 1;28(8):791-801. doi: 10.5551/jat.RV17052. Epub 2021 Apr 28. J Atheroscler Thromb. 2021. PMID: 33907061 Free PMC article. Review.
Sitosterolemia is an inherited metabolic disorder characterized by increased levels of plant sterols, such as sitosterol. ...
Sitosterolemia is an inherited metabolic disorder characterized by increased levels of plant sterols, such as sitosterol. ...
Features of chinese patients with sitosterolemia.
Zhou Z, Su X, Cai Y, Ting TH, Zhang W, Lin Y, Xu A, Mao X, Zeng C, Liu L, Li X. Zhou Z, et al. Lipids Health Dis. 2022 Jan 18;21(1):11. doi: 10.1186/s12944-021-01619-1. Lipids Health Dis. 2022. PMID: 35042526 Free PMC article. Review.
To gain a better understanding of the disease, the current status of diagnosis and treatment of Chinese patients with sitosterolemia was reviewed and summarized. METHOD: Literature search was performed. The clinical features and molecular characteristics of Chinese patient …
To gain a better understanding of the disease, the current status of diagnosis and treatment of Chinese patients with sitosterolemia
Plasma non-cholesterol sterols.
Kuksis A. Kuksis A. J Chromatogr A. 2001 Nov 23;935(1-2):203-36. doi: 10.1016/s0021-9673(01)01226-2. J Chromatogr A. 2001. PMID: 11762775 Review.
Premature atherosclerosis and xanthomatosis occur in two rare lipid storage diseases, Cerebrotendinous xanthomatosis (CTX) and sitosterolemia. In CTX, cholestanol is present in all tissues. In sitosterolemia, dietary campesterol and sitosterol accumulate in plasma a …
Premature atherosclerosis and xanthomatosis occur in two rare lipid storage diseases, Cerebrotendinous xanthomatosis (CTX) and sitosterol
99 results