Hypolipoproteinemia Latest Advances

LDLR-3'UTR Deletions Identified as a Genetic Cause of Hypobetalipoproteinemia: Evidence From Familial and Population-Based Studies.

Journal: Arteriosclerosis, thrombosis, and vascular biology

Published: June 04, 2026

Severe HDL-C Deficiency Caused by Acquired LCAT Deficiency: A Case Report with Lipidomic Profiling and Anti-LCAT Autoantibody Detection.

Journal: Internal medicine (Tokyo, Japan)

Published: May 24, 2026

Lipid lowering therapy in Tangier disease: what is the best association?

Journal: Clinica e investigacion en arteriosclerosis : publicacion oficial de la Sociedad Espanola de Arteriosclerosis

Published: May 12, 2026

Primary hypobetalipoproteinemia as a specific etiology of steatotic liver disease: A meta-analysis.

Journal: Clinics and research in hepatology and gastroenterology

Published: April 19, 2026

Genetic dyslipidemias.

Journal: Annales d'endocrinologie

Published: March 22, 2026

Correction: Miglustat as a Treatment for Adults with Tangier Disease Neuropathy: The MUSTANG N‑of‑1 Trial with 21 months Clinical Observation.

Journal: Neurology and therapy

Published: March 12, 2026

Case report: co-inheritance of familial lecithin-cholesterol acyltransferase deficiency and α0-Thalassemia.

Journal: Frontiers in genetics

Published: February 08, 2026

ABCA1: A Therapeutic Target for Improving Cholesterol Homeostasis in Peripheral Neuropathies.

Journal: Biomolecules

Published: December 12, 2025

Ten-year clinical course of familial lecithin-cholesterol acyltransferase deficiency caused by Cys74Tyr mutation leading to dialysis and multiple systemic complications: a case report.

Journal: CEN case reports

Published: December 12, 2025

Quantitative Assessment of Visual Function in Japanese Patients With Lecithin-Cholesterol Acyltransferase Gene Abnormalities: A Case-Control Study.

Journal: Cureus

Published: November 25, 2025

Diffuse corneal haze: a rare presentation of fish-eye disease.

Journal: Ophthalmic genetics

Published: October 28, 2025

Familial hypobetalipoproteinemia in pediatric patients with fatty liver: an under-recognized cause.

Journal: Frontiers in medicine

Published: October 08, 2025

Hypolipoproteinemia Latest Advances

Find the Latest Research About Hypolipoproteinemia

LDLR-3'UTR Deletions Identified as a Genetic Cause of Hypobetalipoproteinemia: Evidence From Familial and Population-Based Studies.

LDLR-3'UTR Deletions Identified as a Genetic Cause of Hypobetalipoproteinemia: Evidence From Familial and Population-Based Studies.

Severe HDL-C Deficiency Caused by Acquired LCAT Deficiency: A Case Report with Lipidomic Profiling and Anti-LCAT Autoantibody Detection.

Severe HDL-C Deficiency Caused by Acquired LCAT Deficiency: A Case Report with Lipidomic Profiling and Anti-LCAT Autoantibody Detection.

Lipid lowering therapy in Tangier disease: what is the best association?

Lipid lowering therapy in Tangier disease: what is the best association?

Primary hypobetalipoproteinemia as a specific etiology of steatotic liver disease: A meta-analysis.

Primary hypobetalipoproteinemia as a specific etiology of steatotic liver disease: A meta-analysis.

Genetic dyslipidemias.

Genetic dyslipidemias.

Correction: Miglustat as a Treatment for Adults with Tangier Disease Neuropathy: The MUSTANG N‑of‑1 Trial with 21 months Clinical Observation.

Correction: Miglustat as a Treatment for Adults with Tangier Disease Neuropathy: The MUSTANG N‑of‑1 Trial with 21 months Clinical Observation.

Case report: co-inheritance of familial lecithin-cholesterol acyltransferase deficiency and α0-Thalassemia.

Case report: co-inheritance of familial lecithin-cholesterol acyltransferase deficiency and α0-Thalassemia.

ABCA1: A Therapeutic Target for Improving Cholesterol Homeostasis in Peripheral Neuropathies.

ABCA1: A Therapeutic Target for Improving Cholesterol Homeostasis in Peripheral Neuropathies.

Ten-year clinical course of familial lecithin-cholesterol acyltransferase deficiency caused by Cys74Tyr mutation leading to dialysis and multiple systemic complications: a case report.

Ten-year clinical course of familial lecithin-cholesterol acyltransferase deficiency caused by Cys74Tyr mutation leading to dialysis and multiple systemic complications: a case report.

Quantitative Assessment of Visual Function in Japanese Patients With Lecithin-Cholesterol Acyltransferase Gene Abnormalities: A Case-Control Study.

Quantitative Assessment of Visual Function in Japanese Patients With Lecithin-Cholesterol Acyltransferase Gene Abnormalities: A Case-Control Study.

Diffuse corneal haze: a rare presentation of fish-eye disease.

Diffuse corneal haze: a rare presentation of fish-eye disease.

Familial hypobetalipoproteinemia in pediatric patients with fatty liver: an under-recognized cause.

Familial hypobetalipoproteinemia in pediatric patients with fatty liver: an under-recognized cause.