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1978 2
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1990 1
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87 results

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Quoted phrase not found in phrase index: "Hypoalphalipoproteinemia, primary, 2"
Page 1
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.
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.
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 …
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 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 …
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 …
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 …
Peripheral neuropathy in Tangier disease: A literature review and assessment.
Mercan M, Yayla V, Altinay S, Seyhan S. Mercan M, et al. J Peripher Nerv Syst. 2018 Jun;23(2):88-98. doi: 10.1111/jns.12265. Epub 2018 May 8. J Peripher Nerv Syst. 2018. PMID: 29582519 Review.
Syringomyelia-like neuropathy subtype (52.4%) was more frequent than multifocal sensorial and motor neuropathy subtype (26.2%), focal neuropathy subtype (19.1%), and distal symmetric polyneuropathy subtype (2.4%). ...The pattern of electrodiagnostic abnormalities ar …
Syringomyelia-like neuropathy subtype (52.4%) was more frequent than multifocal sensorial and motor neuropathy subtype (26.2%), focal …
Recent progress in the development of radioimmunoassays for human serum lipoproteins.
Karlin JB, Juhn DJ, Goldberg R, Rubenstein AH. Karlin JB, et al. Ann Clin Lab Sci. 1978 Mar-Apr;8(2):142-54. Ann Clin Lab Sci. 1978. PMID: 205163 Review.
Serum apo B concentrations were highest in Type II subjects (Type IIa homozygotes 3.83 +/- 0.43 g per l; Type IIa heterozygotes 2.37 +/- 0.47 g per l) and were less elevated in patients with Type IV and Type V disorders (1.32 +/- 0.21 g per l and 1.26 +/- 0.30 g per l, res …
Serum apo B concentrations were highest in Type II subjects (Type IIa homozygotes 3.83 +/- 0.43 g per l; Type IIa heterozygotes 2.37 …
87 results