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Last Updated: 02/24/2026
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Found 334 publications
Lamin A/C regulates lipid metabolism and inflammation: insights from models of familial partial lipodystrophy 2.
Journal: The Journal of clinical investigation
Published: November 11, 2025
Erratum. Gain of Function NOTCH3 Variants Cause Familial Partial Lipodystrophy Due to Activation of Senescence Pathways. Diabetes 2025;74:427-438.
Journal: Diabetes
Published: October 28, 2025
Epicardial adipose tissue measurement is an interesting biomarker for cardiovascular health in a case control study of patients with familial partial type 2 lipodystrophy.
Journal: Diabetes & metabolism
Published: October 07, 2025
Improvement of severe hypertriglyceridemia in atypical subtype 4 partial lipodystrophy with volanesorsen.
Journal: Journal of clinical lipidology
Published: July 10, 2025
Coincidence of Autoimmune Diabetes Mellitus and Familial Partial Lipodystrophy.
Journal: JCEM case reports
Published: July 08, 2025
Targeting mineralocorticoid receptors to treat metabolic diseases via the adipocyte.
Journal: Endocrinology
Published: July 07, 2025
Interesting Case of Familial Partial Lipodystrophy Syndrome (Type 6) with LIPE Gene Defect: A Case Report.
Journal: The Journal of the Association of Physicians of India
Published: June 24, 2025
Potential Impact of Parental Origin of Inheritance on the Clinical Presentation of Familial Partial Lipodystrophy Type 2 Syndrome.
Journal: Clinical endocrinology
Published: May 21, 2025
Diagnosis and Management of Genetic Lipodystrophy Syndromes and its Implications for Atherosclerosis.
Journal: Current atherosclerosis reports
Published: April 27, 2025
Heterozygous pathogenic PPARG variants in patients with severe hypertriglyceridemia.
Journal: Journal of clinical lipidology
Published: April 22, 2025
Calf skinfold measurements as a diagnostic tool for lipodystrophy syndromes: a cross-sectional study.
Journal: Diabetology & metabolic syndrome
Published: April 16, 2025
Last Updated: 02/24/2026