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97 results

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Quoted phrase not found in phrase index: "Hypoalphalipoproteinemia, primary, 2"
Page 1
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.
Primary and familial hypoalphalipoproteinemia.
Third JL, Montag J, Flynn M, Freidel J, Laskarzewski P, Glueck CJ. Third JL, et al. Metabolism. 1984 Feb;33(2):136-46. doi: 10.1016/0026-0495(84)90126-4. Metabolism. 1984. PMID: 6694557
Our specific aim was to assess within-family clustering of high-density lipoprotein cholesterol (HDLC) levels in kindreds identified through probands with primary hypoalphalipoproteinemia, and to determine whether, and to what degree, familial aggregation of HDLC le …
Our specific aim was to assess within-family clustering of high-density lipoprotein cholesterol (HDLC) levels in kindreds identified through …
Diagnosis and treatment of high density lipoprotein deficiency.
Schaefer EJ, Anthanont P, Diffenderfer MR, Polisecki E, Asztalos BF. Schaefer EJ, et al. Prog Cardiovasc Dis. 2016 Sep-Oct;59(2):97-106. doi: 10.1016/j.pcad.2016.08.006. Epub 2016 Aug 24. Prog Cardiovasc Dis. 2016. PMID: 27565770 Free PMC article. Review.
A machine learning approach to personalized predictors of dyslipidemia: a cohort study.
Gutiérrez-Esparza G, Pulido T, Martínez-García M, Ramírez-delReal T, Groves-Miralrio LE, Márquez-Murillo MF, Amezcua-Guerra LM, Vargas-Alarcón G, Hernández-Lemus E. Gutiérrez-Esparza G, et al. Front Public Health. 2023 Sep 20;11:1213926. doi: 10.3389/fpubh.2023.1213926. eCollection 2023. Front Public Health. 2023. PMID: 37799151 Free PMC article.
METHODS: In this study, we utilized a dataset from a Mexico City cohort consisting of 2,621 participants, men and women aged between 20 and 50 years, with and without some type of dyslipidemia. Our primary objective was to identify potential factors associated with …
METHODS: In this study, we utilized a dataset from a Mexico City cohort consisting of 2,621 participants, men and women aged between …
Analysis of familial hypoalphalipoproteinemia syndromes.
Frohlich J, Pritchard PH. Frohlich J, et al. Mol Cell Biochem. 1992 Aug 18;113(2):141-9. doi: 10.1007/BF00231534. Mol Cell Biochem. 1992. PMID: 1518505 Review.
Familial hypoalphalipoproteinemias (HA) are a heterogenous group of disorders characterized by various degrees of HDL deficiency. Differential diagnosis involves clinical and biochemical evaluation after intervention designed to correct known secondary causes of low HDL. T …
Familial hypoalphalipoproteinemias (HA) are a heterogenous group of disorders characterized by various degrees of HDL deficiency. Dif …
A proteomic approach to identify novel disease biomarkers in LCAT deficiency.
Simonelli S, Ossoli A, Banfi C, Pavanello C, Calabresi L, Gianazza E. Simonelli S, et al. J Proteomics. 2019 Apr 30;198:113-118. doi: 10.1016/j.jprot.2018.12.005. Epub 2018 Dec 6. J Proteomics. 2019. PMID: 30529744 Free article.
Diagnostic and prognostic markers capable of early detecting declining kidney function in these subjects are not available, and the specific serum or urine proteomic signature of LCAT deficient carriers has never been assessed. Taking advantage of a proteomic approach, we perform …
Diagnostic and prognostic markers capable of early detecting declining kidney function in these subjects are not available, and the specific …
Tangier disease: update for 2020.
Hooper AJ, Hegele RA, Burnett JR. Hooper AJ, et al. Curr Opin Lipidol. 2020 Apr;31(2):80-84. doi: 10.1097/MOL.0000000000000669. Curr Opin Lipidol. 2020. PMID: 32022754
Hypoalphalipoproteinemia in populations of Native American ancestry: an opportunity to assess the interaction of genes and the environment.
Aguilar-Salinas CA, Canizales-Quinteros S, Rojas-Martínez R, Mehta R, Villarreal-Molina MT, Arellano-Campos O, Riba L, Gómez-Pérez FJ, Tusié-Luna MT. Aguilar-Salinas CA, et al. Curr Opin Lipidol. 2009 Apr;20(2):92-7. doi: 10.1097/mol.0b013e3283295e96. Curr Opin Lipidol. 2009. PMID: 19280764 Review.
In addition, results from recent genetic studies show that certain hypoalphalipoproteinemia susceptibility alleles are ethnic specific for Native Americans. ...SUMMARY: The assessment of the genetic and environmental determinants of hypoalphalipoproteinemia in popul …
In addition, results from recent genetic studies show that certain hypoalphalipoproteinemia susceptibility alleles are ethnic specifi …
Genetic Lipid Disorders Associated with Atherosclerotic Cardiovascular Disease: Molecular Basis to Clinical Diagnosis and Epidemiologic Burden.
Mszar R, Webb GB, Kulkarni VT, Ahmad Z, Soffer D. Mszar R, et al. Med Clin North Am. 2022 Mar;106(2):325-348. doi: 10.1016/j.mcna.2021.11.009. Epub 2022 Feb 10. Med Clin North Am. 2022. PMID: 35227434 Review.
Genetic lipid disorders, ranging from common dyslipidemias such as familial hypercholesterolemia, lipoprotein (a), and familial combined hyperlipidemia to rare disorders including familial chylomicronemia syndrome and inherited hypoalphalipoproteinemias (ie, Tangier and fi …
Genetic lipid disorders, ranging from common dyslipidemias such as familial hypercholesterolemia, lipoprotein (a), and familial combined hyp …
Diagnosis and management of familial dyslipoproteinemia in children and adolescents.
Kwiterovich PO Jr. Kwiterovich PO Jr. Pediatr Clin North Am. 1990 Dec;37(6):1489-523. doi: 10.1016/s0031-3955(16)37021-3. Pediatr Clin North Am. 1990. PMID: 2259550 Free article. Review.
Children of a parent with documented dyslipoproteinemia or with family history of premature CAD may be screened in the fasting state any time after 2 years of age. Following the exclusion of secondary causes of dyslipoproteinemia, the diagnosis of primary dyslipopro …
Children of a parent with documented dyslipoproteinemia or with family history of premature CAD may be screened in the fasting state any tim …
97 results