Hypolipoproteinemia Latest Advances

Hypocholesterolemia in liver and cardiovascular disease: Friend or foe?

Journal: Journal of internal medicine

Published: August 27, 2026

Comorbid Abetalipoproteinemia and Neurofibromatosis Type 1: Potential Clinical Implications of an Ultrarare Co-occurrence.

Journal: Annals of internal medicine. Clinical cases

Published: August 19, 2026

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

Chorea-Acanthocytosis Without Acanthocytosis: Sensory Neuronopathy and Epilepsy as Prominent Features From a Novel VPS13A Variant.

Journal: Clinical genetics

Published: May 19, 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

Neuropathy-predominant and hyperkinetic-dystonic presentations in two siblings with a homozygous VPS13A variant: long-term follow-up and family-based clinical analysis.

Journal: BMC neurology

Published: May 05, 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

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

Case Report: clinical manifestations and imaging features associated with PANK2 c.940C>T variant in PKAN with symmetric basal ganglia calcification.

Journal: Frontiers in genetics

Published: January 20, 2026

Muscle MRI in a patient with chorea acanthocytosis.

Journal: Neuromuscular disorders : NMD

Published: January 02, 2026

Hypolipoproteinemia Latest Advances

Find the Latest Research About Hypolipoproteinemia

Hypocholesterolemia in liver and cardiovascular disease: Friend or foe?

Hypocholesterolemia in liver and cardiovascular disease: Friend or foe?

Comorbid Abetalipoproteinemia and Neurofibromatosis Type 1: Potential Clinical Implications of an Ultrarare Co-occurrence.

Comorbid Abetalipoproteinemia and Neurofibromatosis Type 1: Potential Clinical Implications of an Ultrarare Co-occurrence.

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.

Chorea-Acanthocytosis Without Acanthocytosis: Sensory Neuronopathy and Epilepsy as Prominent Features From a Novel VPS13A Variant.

Chorea-Acanthocytosis Without Acanthocytosis: Sensory Neuronopathy and Epilepsy as Prominent Features From a Novel VPS13A Variant.

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

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

Neuropathy-predominant and hyperkinetic-dystonic presentations in two siblings with a homozygous VPS13A variant: long-term follow-up and family-based clinical analysis.

Neuropathy-predominant and hyperkinetic-dystonic presentations in two siblings with a homozygous VPS13A variant: long-term follow-up and family-based clinical analysis.

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.

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.

Case Report: clinical manifestations and imaging features associated with PANK2 c.940C>T variant in PKAN with symmetric basal ganglia calcification.

Case Report: clinical manifestations and imaging features associated with PANK2 c.940C>T variant in PKAN with symmetric basal ganglia calcification.

Muscle MRI in a patient with chorea acanthocytosis.

Muscle MRI in a patient with chorea acanthocytosis.