Disease: Norum disease
- A High-Throughput NMR Method for Lipoprotein-X Quantification
- A novel homozygous frameshift mutation in the APOA1 gene associated with marked high-density lipoprotein deficiency
- A rare case of renal involvement in Lecithin-Cholesterol Acyltransferase (LCAT) deficiency: lessons for the clinical nephrologist
- Abnormal Lipoproteins Trigger Oxidative Stress-Mediated Apoptosis of Renal Cells in LCAT Deficiency
- Alpha-2-adrenergic receptor agonists for the prevention of delirium and cognitive decline after open heart surgery (ALPHA2PREVENT): protocol for a multicentre randomised controlled trial
- Dynamics of Serologic Change to Gluten in Celiac Disease Patients
- Epidermal 1-O-acylceramides appear with the establishment of the water permeability barrier in mice and are produced by maturating keratinocytes
- Familial LCAT Deficiency and Low HDL-C Levels: In silico Characterization of Two Rare LCAT Missense Mutations
- Familial lecithin-cholesterol acyltransferase deficiency: If so rare, why so frequent in the state of PiauĂ, northeastern Brazil?
- First-in-human autologous implantation of genetically modified adipocytes expressing LCAT for the treatment of familial LCAT deficiency
- Glomerular lipidosis as a feature of renal-limited macrophage activation syndrome in a transplanted kidney: a case report
- Latiglutenase Protects the Mucosa and Attenuates Symptom Severity in Patients With Celiac Disease Exposed to a Gluten Challenge
- LCAT-trial-24 weeks: Protocol for a clinical study to evaluate the safety of regenerative medicine and gene therapy by the autologous transplantation of human lecithin:cholesterol acyltransferase gene-transduced human pre-adipocytes
- Lipoprotein X-Induced Hyperlipidemia
- Megaprosthesis for Metastatic Bone Disease-A Comparative Analysis
- Novel regional longitudinal strain by speckle tracking to detect significant coronary artery disease in patients admitted to the emergency department for chest pain suggestive of acute coronary syndrome
- Novel therapeutic opportunities for familial lecithin:cholesterol acyltransferase deficiency: promises and challenges
- Plasma FA composition in familial LCAT deficiency indicates SOAT2-derived cholesteryl ester formation in humans
- Rapidly progressive renal failure to reveal LCAT deficiency in an Algerian family
- Two Cases of Acquired High-Density Lipoprotein Deficiency with Immunoglobulin G4-Related Lecithin-Cholesterol Acyltransferase Autoantibody
- Two novel variants in the lecithin:cholesterol acyltransferase gene resulted in classic LCAT deficiency