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Year Number of Results
1975 1
1980 1
1982 1
1986 1
1991 1
1993 2
1996 1
1998 2
1999 1
2001 4
2002 1
2004 1
2005 1
2006 1
2007 12
2008 1
2010 1
2012 1
2013 3
2014 6
2015 5
2016 4
2017 3
2018 3
2019 1
2020 2
2021 5
2022 3
2023 2

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64 results

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Page 1
Guidance for the diagnosis and treatment of hypolipidemia disorders.
Bredefeld C, Hussain MM, Averna M, Black DD, Brin MF, Burnett JR, Charrière S, Cuerq C, Davidson NO, Deckelbaum RJ, Goldberg IJ, Granot E, Hegele RA, Ishibashi S, Karmally W, Levy E, Moulin P, Okazaki H, Poinsot P, Rader DJ, Takahashi M, Tarugi P, Traber MG, Di Filippo M, Peretti N. Bredefeld C, et al. J Clin Lipidol. 2022 Nov-Dec;16(6):797-812. doi: 10.1016/j.jacl.2022.08.009. Epub 2022 Sep 29. J Clin Lipidol. 2022. PMID: 36243606 Free article. Review.
Black Garlic and Its Bioactive Compounds on Human Health Diseases: A Review.
Ahmed T, Wang CK. Ahmed T, et al. Molecules. 2021 Aug 19;26(16):5028. doi: 10.3390/molecules26165028. Molecules. 2021. PMID: 34443625 Free PMC article. Review.
Most of these benefits can be attributed to its anti-oxidation, anti-inflammation, anti-obesity, hepatoprotection, hypolipidemia, anti-cancer, anti-allergy, immunomodulation, nephroprotection, cardiovascular protection, and neuroprotection. ...
Most of these benefits can be attributed to its anti-oxidation, anti-inflammation, anti-obesity, hepatoprotection, hypolipidemia, ant …
Hypotriglyceridemias/hypolipidemias.
Martínez-Hervás S, Real-Collado JT, Ascaso-Gimilio JF. Martínez-Hervás S, et al. Clin Investig Arterioscler. 2021 May;33 Suppl 2:63-68. doi: 10.1016/j.arteri.2020.12.011. Clin Investig Arterioscler. 2021. PMID: 34006356 Review. English, Spanish.
Familial combined hypolipidemia: angiopoietin-like protein-3 deficiency.
Arca M, D'Erasmo L, Minicocci I. Arca M, et al. Curr Opin Lipidol. 2020 Apr;31(2):41-48. doi: 10.1097/MOL.0000000000000668. Curr Opin Lipidol. 2020. PMID: 32022755 Review.
RECENT FINDINGS: Experimental studies have further illustrated the complex interplay between ANGPTL3 and ANGPTL4-8 in orchestrating lipid transport in different nutritional status. Individuals with familial combined hypolipidemia due to homozygous loss-of-function mutation …
RECENT FINDINGS: Experimental studies have further illustrated the complex interplay between ANGPTL3 and ANGPTL4-8 in orchestrating lipid tr …
Current Diagnosis and Management of Abetalipoproteinemia.
Takahashi M, Okazaki H, Ohashi K, Ogura M, Ishibashi S, Okazaki S, Hirayama S, Hori M, Matsuki K, Yokoyama S, Harada-Shiba M. Takahashi M, et al. J Atheroscler Thromb. 2021 Oct 1;28(10):1009-1019. doi: 10.5551/jat.RV17056. Epub 2021 May 16. J Atheroscler Thromb. 2021. PMID: 33994405 Free PMC article. Review.
Deficiency of microsomal triglyceride transfer protein (MTTP) abrogates the assembly of apolipoprotein (apo) B-containing lipoprotein in the intestine and liver, resulting in malabsorption of fat and fat-soluble vitamins and severe hypolipidemia. Patients with ABL typicall …
Deficiency of microsomal triglyceride transfer protein (MTTP) abrogates the assembly of apolipoprotein (apo) B-containing lipoprotein in the …
Hypobetalipoproteinemia and abetalipoproteinemia.
Welty FK. Welty FK. Curr Opin Lipidol. 2014 Jun;25(3):161-8. doi: 10.1097/MOL.0000000000000072. Curr Opin Lipidol. 2014. PMID: 24751931 Free PMC article. Review.
PURPOSE OF REVIEW: Several mutations in the apoB, proprotein convertase subtilisin/kexin type 9 (PCSK9), and MTP genes result in low or absent levels of apoB and LDL-cholesterol in plasma, which cause familial hypobetalipoproteinemia and abetalipoproteinemia. Mutations in the ANG …
PURPOSE OF REVIEW: Several mutations in the apoB, proprotein convertase subtilisin/kexin type 9 (PCSK9), and MTP genes result in low or abse …
Endocrine and metabolic disorders in patients with Gaucher disease type 1: a review.
Kałużna M, Trzeciak I, Ziemnicka K, Machaczka M, Ruchała M. Kałużna M, et al. Orphanet J Rare Dis. 2019 Dec 2;14(1):275. doi: 10.1186/s13023-019-1211-5. Orphanet J Rare Dis. 2019. PMID: 31791361 Free PMC article. Review.
BACKGROUND: Gaucher disease (GD) is one of the most prevalent lysosomal storage diseases and is associated with hormonal and metabolic abnormalities, including nutritional status disorders, hypermetabolic state with high resting energy expenditures, peripheral insulin resistance, …
BACKGROUND: Gaucher disease (GD) is one of the most prevalent lysosomal storage diseases and is associated with hormonal and metabolic abnor …
The dementias.
Ritchie K, Lovestone S. Ritchie K, et al. Lancet. 2002 Nov 30;360(9347):1759-66. doi: 10.1016/S0140-6736(02)11667-9. Lancet. 2002. PMID: 12480441 Review.
Neurochemical and neurobiological research has led to advances in understanding causes of dementia, and functional imaging has allowed identification of possible biomarkers; from these, a range of potential treatment approaches have arisen that focus on enhancement of neurotransm …
Neurochemical and neurobiological research has led to advances in understanding causes of dementia, and functional imaging has allowed ident …
Healthy Uses for Garlic.
White D. White D. Nurs Clin North Am. 2021 Mar;56(1):153-156. doi: 10.1016/j.cnur.2020.12.001. Nurs Clin North Am. 2021. PMID: 33549282 Review.
Hypolipidemia in a Special Operations Candidate: Case Report and Review of the Literature.
Strain JE 2nd, Vigilante JA, DiGeorge NW. Strain JE 2nd, et al. J Spec Oper Med. 2015 Winter;15(4):1-5. doi: 10.55460/8AF7-1QDL. J Spec Oper Med. 2015. PMID: 26630090 Review.
BACKGROUND: A 19-year-old male military recruit who presented for a screening physical for US Naval Special Warfare Duty was found to have hypolipidemia. Medical history revealed mildly increased frequency of bowel movements, but was otherwise unremarkable. ...Keywords inc …
BACKGROUND: A 19-year-old male military recruit who presented for a screening physical for US Naval Special Warfare Duty was found to have …
64 results