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Sitosterolemia.
Tada H, Kojima N, Takamura M, Kawashiri MA. Tada H, et al. Adv Clin Chem. 2022;110:145-169. doi: 10.1016/bs.acc.2022.06.006. Epub 2022 Aug 9. Adv Clin Chem. 2022. PMID: 36210074
Sitosterolemia is an inherited metabolic disorder characterized by increased levels of plant sterols, such as sitosterol. ...Unlike cases of homozygous FH, dietary counseling is quite effective in reducing the LDL cholesterol as well as sitosterol of patients with sitos
Sitosterolemia is an inherited metabolic disorder characterized by increased levels of plant sterols, such as sitosterol. ...Unlike c
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
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
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.
BACKGROUND: Sitosterolemia is a lipid disorder characterized by the accumulation of phytosterols in plasma and organs, caused by mutations in the ABCG5 and/or ABCG8 genes. ...The clinical features and molecular characteristics of Chinese patients with sitosterolemia
BACKGROUND: Sitosterolemia is a lipid disorder characterized by the accumulation of phytosterols in plasma and organs, caused by muta …
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. ...
Xenosterolemia in clinical practice: what is in a name?
Loh WJ, Watts GF. Loh WJ, et al. Curr Opin Endocrinol Diabetes Obes. 2023 Apr 1;30(2):123-127. doi: 10.1097/MED.0000000000000795. Epub 2022 Dec 29. Curr Opin Endocrinol Diabetes Obes. 2023. PMID: 36597814 Review.
SUMMARY: Measurement of plasma phytosterols can identify individuals with xenosterolemia (or phytosterolemia). This may be clinically useful in four ways: Establishing a diagnosis and informing management of patients with homozygous phytosterolemia; Providing a comp …
SUMMARY: Measurement of plasma phytosterols can identify individuals with xenosterolemia (or phytosterolemia). This may be clinically …
The ABCs of Sterol Transport.
Plummer AM, Culbertson AT, Liao M. Plummer AM, et al. Annu Rev Physiol. 2021 Feb 10;83:153-181. doi: 10.1146/annurev-physiol-031620-094944. Epub 2020 Nov 3. Annu Rev Physiol. 2021. PMID: 33141631 Review.
ATP-binding cassette (ABC) transporters play several critical roles in this process, and mutations in these sterol transporters lead to disorders such as Tangier disease and sitosterolemia. Biochemical and structural information on ABC sterol transporters is beginning to e …
ATP-binding cassette (ABC) transporters play several critical roles in this process, and mutations in these sterol transporters lead to diso …
Orbital involvement of Sitosterolemia.
Okafor LO, Bowyer J, Thaung C, Murphy E, Verity DH. Okafor LO, et al. Orbit. 2022 Feb;41(1):118-122. doi: 10.1080/01676830.2020.1820534. Epub 2020 Sep 17. Orbit. 2022. PMID: 32942937
Sitosterolemia is a rare inherited condition in which plant sterols are stored and deposited in the tissues. ...Magnetic resonance imaging identified a soft tissue mass within the orbit, with subsequent biopsy confirming a xanthogranulomatous process consistent with the di
Sitosterolemia is a rare inherited condition in which plant sterols are stored and deposited in the tissues. ...Magnetic resonance im
Sitosterolemia: Twenty Years of Discovery of the Function of ABCG5ABCG8.
Williams K, Segard A, Graf GA. Williams K, et al. Int J Mol Sci. 2021 Mar 5;22(5):2641. doi: 10.3390/ijms22052641. Int J Mol Sci. 2021. PMID: 33807969 Free PMC article. Review.
Sitosterolemia is a lipid disorder characterized by the accumulation of dietary xenosterols in plasma and tissues caused by mutations in either ABCG5 or ABCG8. ...
Sitosterolemia is a lipid disorder characterized by the accumulation of dietary xenosterols in plasma and tissues caused by mutations
68 results