Disease: Familial Hypoalphalipoproteinemia
- A case of mesenteric panniculitis in a patient with Tangier disease
- A case of premature and recurrent myocardial infarction associated with ABCA.1 gene mutation
- A case report of Tangier disease presents with acute sensorimotor polyneuropathy and its treatment approach
- A novel homozygous ABCA1 variant in an asymptomatic man with profound hypoalphalipoproteinemia
- A novel homozygous frameshift mutation in the APOA1 gene associated with marked high-density lipoprotein deficiency
- A novel homozygous mutation causing lecithin-cholesterol acyltransferase deficiency in a proband of Romanian origin with a record of extreme gestational hyperlipidemia
- A novel pathogenic variant in LCAT causing FLD. A case report
- A novel splicing mutation in the ABCA1 gene, causing Tangier disease and familial HDL deficiency in a large family
- A proteomic approach to identify novel disease biomarkers in LCAT deficiency
- A rare case of nephrotic syndrome and Tangier disease
- A rare case of renal involvement in Lecithin-Cholesterol Acyltransferase (LCAT) deficiency: lessons for the clinical nephrologist
- A systematic review of the natural history and biomarkers of primary lecithin:cholesterol acyltransferase deficiency
- Accelerated Atherogenicity in Tangier Disease
- Administration of the High-Density Lipoprotein Mimetic CER-001 for Inherited Lecithin-Cholesterol Acyltransferase Deficiency
- An abnormal lipid profile: when to perform additional research for a genetic cause?
- Association of Severity of Lower Extremity Arterial Disease and Overactive Bladder Syndrome: A Cross Sectional Study
- ATP-binding cassette transporter A1: A promising therapy target for prostate cancer
- Atypical Presentation of Tangier Disease-Expanding the Clinical Spectrum
- Biochemical, Clinical, and Genetic Characteristics of Mexican Patients with Primary Hypertriglyceridemia, Including the First Case of Hyperchylomicronemia Syndrome Due to GPIHBP1 Deficiency
- Can Tangier disease cause male infertility? A case report and an overview on genetic causes of male infertility and hormonal axis involved
- Case Report: Management of Corneal Clouding from Lecithin: Cholesterol Acyltransferase Deficiency
- CER-001 ameliorates lipid profile and kidney disease in a mouse model of familial LCAT deficiency
- Cholesterol Efflux Pathways Suppress Inflammasome Activation, NETosis, and Atherogenesis
- Clinical Dilemma of Corneal Opacity, Very Low High-density Lipoprotein, and Nephrotic Syndrome: Mystery Revealed
- Complete and Partial Lecithin:Cholesterol Acyltransferase Deficiency Is Differentially Associated With Atherosclerosis
- Correction of Familial LCAT Deficiency by AAV-hLCAT Prevents Renal Injury and Atherosclerosis in Hamsters-Brief Report
- Current Diagnosis and Management of Tangier Disease
- Current Status of Familial LCAT Deficiency in Japan
- Dietary and Health Characteristics of Korean Adults According to the Level of Energy Intake from Carbohydrate: Analysis of the 7th (2016-2017) Korea National Health and Nutrition Examination Survey Data
- Early-onset atherosclerosis in a patient with Tangier disease: Not all that is gold glitters
- Effect of a common missense variant in LIPA gene on fatty liver disease and lipid phenotype: New perspectives from a single-center observational study
- Esterification of 4β-hydroxycholesterol and other oxysterols in human plasma occurs independently of LCAT
- Familial LCAT deficiency and cardiovascular disease: the game is not over. A case of dramatic multivessel atherosclerosis
- Genetic and secondary causes of severe HDL deficiency and cardiovascular disease
- Genetic Lipid Disorders Associated with Atherosclerotic Cardiovascular Disease: Molecular Basis to Clinical Diagnosis and Epidemiologic Burden
- Genetic, biochemical, and clinical features of LCAT deficiency: update for 2020
- Glomerulopathy associated with lecithin-cholesterol-acyltransferase deficiency: A case report and literature review
- HIV disease, metabolic dysfunction and atherosclerosis: A three year prospective study
- Hypoalphalipoproteinemia
- Hypoalphalipoproteinemia
- Hypoalphalipoproteinemia and BRAF(V600E) Mutation Are Major Predictors of Aortic Infiltration in the Erdheim-Chester Disease
- Hypoalphalipoproteinemia and BRAF<sup>V600E</sup> Mutation Are Major Predictors of Aortic Infiltration in the Erdheim-Chester Disease
- Hypotriglyceridemias/hypolipidemias
- Identification and functional analysis of missense mutations in the lecithin cholesterol acyltransferase gene in a Chilean patient with hypoalphalipoproteinemia
- Identification of the first Tangier disease patient in Lebanon carrying a new pathogenic variant in ABCA1
- Immune-mediated acquired lecithin-cholesterol acyltransferase deficiency: A case report and literature review
- Impact of apolipoprotein A1- or lecithin:cholesterol acyltransferase-deficiency on white adipose tissue metabolic activity and glucose homeostasis in mice
- Increased carotid intima-media thickness and cardiometabolic risk factors are associated with IL-6 gene polymorphisms in Mexican individuals: The Genetics of Atherosclerotic Disease Mexican study
- Interleukin 6 polymorphisms are associated with cardiovascular risk factors in premature coronary artery disease patients and healthy controls of the GEA Mexican study
- Intravascular lithotripsy to treat an ostial left main coronary artery stenosis due to porcelain aorta in a patient with congenital high-density lipoprotein deficiency
- Is Low-Density Lipoprotein Cholesterol the Key to Interpret the Role of Lecithin:Cholesterol Acyltransferase in Atherosclerosis?
- Large-scale deletions of the <em>ABCA1</em> gene in patients with hypoalphalipoproteinemia
- Large-scale deletions of the ABCA1 gene in patients with hypoalphalipoproteinemia
- LCAT deficiency as a cause of proteinuria and corneal opacification
- LCAT deficiency: a systematic review with the clinical and genetic description of Mexican kindred
- LCAT Enzyme Replacement Therapy Reduces LpX and Improves Kidney Function in a Mouse Model of Familial LCAT Deficiency
- LCAT- targeted therapies: Progress, failures and future
- LCAT, ApoD, and ApoA1 Expression and Review of Cholesterol Deposition in the Cornea
- Lipoprotein-X fifty years after its original discovery
- Longitudinal analysis of clinical and laboratory biomarkers in a patient with familial lecithin: Cholesterol acyltransferase deficiency (FLD) and accelerated eGFR decline: A case study
- Low high-density lipoprotein and increased risk of several cancers: 2 population-based cohort studies including 116,728 individuals
- Lp8 is potentially associated with partial lecithin:cholesterol acyltransferase deficiency in a patient with primary biliary cirrhosis
- Metabolic syndrome and its components are associated with non-arteritic anterior ischaemic optic neuropathy
- Metabolomic analysis of plasma from normal-weight adults with hypo-HDL cholesterolemia by UPLC-QTOF MS
- Naturally Occurring Variants in LRP1 (Low-Density Lipoprotein Receptor-Related Protein 1) Affect HDL (High-Density Lipoprotein) Metabolism Through ABCA1 (ATP-Binding Cassette A1) and SR-B1 (Scavenger Receptor Class B Type 1) in Humans
- Nerve high-resolution ultrasonography in tangier disease
- No benefit of HDL mimetic CER-001 on carotid atherosclerosis in patients with genetically determined very low HDL levels
- Novel lecithin: cholesterol acyltransferase-based therapeutic approaches
- Novel therapeutic opportunities for familial lecithin:cholesterol acyltransferase deficiency: promises and challenges
- NUtraceutical TReatment for hYpercholesterolemia in HIV-infected patients: The NU-TRY(HIV) randomized cross-over trial
- Ocular and Genetic Characteristics Observed in Two Cases of Fish-Eye Disease
- Paradoxical fall in proteinuria during pregnancy in an LCAT-deficient patient-A case report
- Peripheral neuropathy in Tangier disease: A literature review and assessment
- Plasma FA composition in familial LCAT deficiency indicates SOAT2-derived cholesteryl ester formation in humans
- Plasma lipoprotein-X quantification on filipin-stained gels: monitoring recombinant LCAT treatment ex vivo
- Polygenic scores for dyslipidemia: the emerging genomic model of plasma lipoprotein trait inheritance
- Progress in finding pathogenic DNA copy number variations in dyslipidemia
- Progression of chronic kidney disease in familial LCAT deficiency: a follow-up of the Italian cohort
- Rapidly progressive renal failure to reveal LCAT deficiency in an Algerian family
- Rare Diseases Related with Lipoprotein Metabolism
- Rare primary dyslipidaemias associated with low LDL and HDL cholesterol values in Portugal
- Selective Correction of Genotype Yield by Probucol in HDL-Deficient Mice Propagation
- Sensory-motor not length-dependent multineuropathy followed by the syringomyelia-like phenotype: a novel presentation of Tangier disease
- Sex-Specific Association between Serum Vitamin D Status and Lipid Profiles: A Cross-Sectional Study of a Middle-Aged and Elderly Chinese Population
- Spontaneous Atherosclerosis in Aged LCAT-Deficient Hamsters With Enhanced Oxidative Stress-Brief Report
- Steryl ester synthesis, storage and hydrolysis: A contribution to sterol homeostasis
- Structural determinants in ApoA-I amyloidogenic variants explain improved cholesterol metabolism despite low HDL levels
- Tangier disease in family with the phenotype of familial hypercholesterolemia
- Tangier disease may cause early onset of atherosclerotic cerebral infarction: A case report
- Tangier disease: update for 2020
- The HDL mimetic CER-001 remodels plasma lipoproteins and reduces kidney lipid deposits in inherited lecithin:cholesterol acyltransferase deficiency
- The P274S Mutation of Lecithin-Cholesterol Acyltransferase (LCAT) and Its Clinical Manifestations in a Large Kindred
- The Role of the ATP-Binding Cassette A1 (ABCA1) in Human Disease
- Two Cases of Acquired High-Density Lipoprotein Deficiency with Immunoglobulin G4-Related Lecithin-Cholesterol Acyltransferase Autoantibody
- Unusual White-Yellowish Dots in the Colon Reveal a Rare Metabolic Disease
- Unusual yellow scaly colonic mucosal appearance: Tangier disease
- Valve Replacement for Severe Aortic Stenosis in a Patient with Tangier Disease
- Very low HDL levels: clinical assessment and management
- What Kind of Probucol Affects Normalizing Male Birth?
- Whole-exome sequencing reveals damaging gene variants associated with hypoalphalipoproteinemia