Hypolipoproteinemia Latest Advances

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

Identification of a novel apoB variant in a family exhibiting hypocholesterolemia: Mechanistic insights.

Journal: Journal of clinical lipidology

Published: December 15, 2025

Familial hypercholesterolemia concealed by a protein-truncating variant of PCSK9.

Journal: Journal of clinical lipidology

Published: December 15, 2025

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

Journal: Biomolecules

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

A Novel Missense Mutation in a Compound Heterozygous Patient with Fish-Eye Disease: A Case Report.

Journal: Case reports in ophthalmology

Published: September 28, 2025

Lecithin-Cholesterol Acyltransferase Deficiency as a Rare Cause of Bilateral Corneal Opacities: A Case Report of a Novel Frameshift Mutation.

Journal: Case reports in ophthalmology

Published: September 19, 2025

Deficiency of the Tangier Disease Gene Abca1 Is Associated With Microglial Defects in Mice.

Journal: International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience

Published: September 11, 2025

A Case of Acquired LCAT Deficiency with the Discrepancy between Spontaneous Resolution of Proteinuria and Continually Low HDL Cholesterol Levels.

Journal: Journal of atherosclerosis and thrombosis

Published: September 10, 2025

How urban park exposure shapes dyslipidemia risk: Evidence from mobility data in Seoul, South Korea.

Journal: Social science & medicine (1982)

Published: September 04, 2025

Hypolipoproteinemia Latest Advances

Find the Latest Research About Hypolipoproteinemia

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.

Identification of a novel apoB variant in a family exhibiting hypocholesterolemia: Mechanistic insights.

Identification of a novel apoB variant in a family exhibiting hypocholesterolemia: Mechanistic insights.

Familial hypercholesterolemia concealed by a protein-truncating variant of PCSK9.

Familial hypercholesterolemia concealed by a protein-truncating variant of PCSK9.

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

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

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.

A Novel Missense Mutation in a Compound Heterozygous Patient with Fish-Eye Disease: A Case Report.

A Novel Missense Mutation in a Compound Heterozygous Patient with Fish-Eye Disease: A Case Report.

Lecithin-Cholesterol Acyltransferase Deficiency as a Rare Cause of Bilateral Corneal Opacities: A Case Report of a Novel Frameshift Mutation.

Lecithin-Cholesterol Acyltransferase Deficiency as a Rare Cause of Bilateral Corneal Opacities: A Case Report of a Novel Frameshift Mutation.

Deficiency of the Tangier Disease Gene Abca1 Is Associated With Microglial Defects in Mice.

Deficiency of the Tangier Disease Gene Abca1 Is Associated With Microglial Defects in Mice.

A Case of Acquired LCAT Deficiency with the Discrepancy between Spontaneous Resolution of Proteinuria and Continually Low HDL Cholesterol Levels.

A Case of Acquired LCAT Deficiency with the Discrepancy between Spontaneous Resolution of Proteinuria and Continually Low HDL Cholesterol Levels.

How urban park exposure shapes dyslipidemia risk: Evidence from mobility data in Seoul, South Korea.

How urban park exposure shapes dyslipidemia risk: Evidence from mobility data in Seoul, South Korea.