Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1974 1
1975 2
1976 4
1977 1
1978 5
1979 3
1980 6
1981 3
1982 4
1984 2
1985 3
1986 8
1987 3
1988 5
1989 1
1990 4
1992 3
1993 4
1994 8
1995 3
1996 1
1997 5
1998 6
1999 3
2000 12
2001 12
2002 8
2003 4
2004 10
2005 5
2006 7
2007 9
2008 2
2009 2
2010 4
2011 7
2012 9
2013 7
2014 10
2015 2
2016 2
2017 2
2018 3
2019 3
2020 2
2021 5
2022 4
2023 2
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

207 results

Results by year

Filters applied: . Clear all
Page 1
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.
Within them, we find two groups: hypobetalipoproteinemias (HBL), due to a decrease in the plasma concentration of lipoproteins containing apolipoprotein B, and hypoalphalipoproteinemias. Hypolipoproteinemias can be classified according to their origin, into primary and sec …
Within them, we find two groups: hypobetalipoproteinemias (HBL), due to a decrease in the plasma concentration of lipoproteins containing ap …
Familial hypoalphalipoproteinemia.
Glueck CJ, Melser MA, Borecki IB, Third JL, Rao DC, Laskarzewski PM. Glueck CJ, et al. Adv Exp Med Biol. 1986;201:83-92. doi: 10.1007/978-1-4684-1262-8_8. Adv Exp Med Biol. 1986. PMID: 3541525 Review. No abstract available.
Familial hypoalphalipoproteinemias.
Frohlich J, Westerlund J, Sparks D, Pritchard PH. Frohlich J, et al. Clin Invest Med. 1990 Aug;13(4):202-10. Clin Invest Med. 1990. PMID: 2119926 Review.
The familial hypoalphalipoproteinemias are a heterogeneous group of rare lipoprotein disorders characterized by extremely low levels of plasma high density lipoproteins (HDL) and, in most cases, autosomal recessive inheritance. ...This is true of Tangier disease, Fi …
The familial hypoalphalipoproteinemias are a heterogeneous group of rare lipoprotein disorders characterized by extremely low …
HDL genetic defects.
Nair DR, Nair A, Jain A. Nair DR, et al. Curr Pharm Des. 2014;20(40):6230-7. doi: 10.2174/1381612820666140620122412. Curr Pharm Des. 2014. PMID: 24953397 Review.
The genetic defects affecting plasma HDL-C concentrations do not always show a consistent relationship with atherosclerosis. Familial hypoalphalipoproteinaemia is associated with mutations in genes responsible for the transport proteins or the enzymes involved in th …
The genetic defects affecting plasma HDL-C concentrations do not always show a consistent relationship with atherosclerosis. Familial
ABCA1 and atherosclerosis.
Soumian S, Albrecht C, Davies AH, Gibbs RG. Soumian S, et al. Vasc Med. 2005 May;10(2):109-19. doi: 10.1191/1358863x05vm593ra. Vasc Med. 2005. PMID: 16013195 Review.
Very low HDL levels: clinical assessment and management.
Bonilha I, Luchiari B, Nadruz W, Sposito AC. Bonilha I, et al. Arch Endocrinol Metab. 2023 Jan 18;67(1):3-18. doi: 10.20945/2359-3997000000585. Arch Endocrinol Metab. 2023. PMID: 36651718 Free PMC article. Review.
In individuals with very low high-density lipoprotein (HDL-C) cholesterol, such as Tangier disease, LCAT deficiency, and familial hypoalphalipoproteinemia, there is an increased risk of premature atherosclerosis. ...
In individuals with very low high-density lipoprotein (HDL-C) cholesterol, such as Tangier disease, LCAT deficiency, and familial
Tangier disease and ABCA1.
Oram JF. Oram JF. Biochim Biophys Acta. 2000 Dec 15;1529(1-3):321-30. doi: 10.1016/s1388-1981(00)00157-8. Biochim Biophys Acta. 2000. PMID: 11111099 Review.
Mutations in the ATP binding cassette transporter ABCA1 cause Tangier disease and other familial HDL deficiencies. ABCA1 controls a cellular pathway that secretes cholesterol and phospholipids to lipid-poor apolipoproteins. ...
Mutations in the ATP binding cassette transporter ABCA1 cause Tangier disease and other familial HDL deficiencies. ABCA1 controls a c …
Progress in finding pathogenic DNA copy number variations in dyslipidemia.
Iacocca MA, Dron JS, Hegele RA. Iacocca MA, et al. Curr Opin Lipidol. 2019 Apr;30(2):63-70. doi: 10.1097/MOL.0000000000000581. Curr Opin Lipidol. 2019. PMID: 30664016 Review.
RECENT FINDINGS: Until last year, only the LDLR and LPA genes were appreciated as loci within which clinically relevant CNVs contributed to familial hypercholesterolemia and variation in Lp(a) levels, respectively. Since 2017, next-generation sequencing panels have identif …
RECENT FINDINGS: Until last year, only the LDLR and LPA genes were appreciated as loci within which clinically relevant CNVs contributed to …
Novel therapeutic opportunities for familial lecithin:cholesterol acyltransferase deficiency: promises and challenges.
Vitali C, Rader DJ, Cuchel M. Vitali C, et al. Curr Opin Lipidol. 2023 Apr 1;34(2):35-43. doi: 10.1097/MOL.0000000000000864. Epub 2022 Dec 6. Curr Opin Lipidol. 2023. PMID: 36473023 Review.
PURPOSE OF REVIEW: Genetic lecithin:cholesterol acyltransferase (LCAT) deficiency is a rare, inherited, recessive disease, which manifests as two different syndromes: Familial LCAT deficiency (FLD) and Fish-eye disease (FED), characterized by low HDL-C and corneal opacity. …
PURPOSE OF REVIEW: Genetic lecithin:cholesterol acyltransferase (LCAT) deficiency is a rare, inherited, recessive disease, which manifests a …
Reverse cholesterol transport fluxes.
Hellerstein M, Turner S. Hellerstein M, et al. Curr Opin Lipidol. 2014 Feb;25(1):40-7. doi: 10.1097/MOL.0000000000000050. Curr Opin Lipidol. 2014. PMID: 24362356 Review.
207 results