Familial Partial Lipodystrophy Latest Advances
Find the Latest Research About Familial Partial Lipodystrophy
Last Updated: 06/30/2026
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Found 351 publications
Molecular insight into the activator and deactivator mutations of peroxisome proliferator-activated receptor gamma.
Journal: Journal of biomolecular structure & dynamics
Published: June 05, 2026
Acanthosis nigricans as a diagnostic clue for familial partial lipodystrophy type 2: a case report with review of literature on Japanese cases.
Journal: Endocrine journal
Published: May 13, 2026
Lipodystrophies in Clinical Practice: A Case Series From a Local Health Unit in Portugal.
Journal: Cureus
Published: February 17, 2026
Bone phenotype in familial partial lipodystrophy type 2: Insulin resistance and sclerostin.
Journal: Diabetes & metabolism
Published: February 13, 2026
A Novel PPARG R212W Variant Causes Familial Partial Lipodystrophy Type 3: Clinical Presentation and Functional Characterization.
Journal: International journal of molecular sciences
Published: January 15, 2026
Familial partial lipodystrophy type 2 associated with a novel LMNA variant (c.604G>C; p.Glu202Gln): a Colombian family case series.
Journal: Frontiers in endocrinology
Published: January 15, 2026
Familial Generalized and Partial Lipodystrophies Due to Rare Biallelic Variants in LMNA.
Journal: International journal of molecular sciences
Published: December 18, 2025
Lamin A/C in health, laminopathies, and familial partial lipodystrophy 2.
Journal: Trends in endocrinology and metabolism: TEM
Published: December 01, 2025
A simple and robust reporter-based framework for deep functional characterization of PPARγ mutants.
Journal: Endocrinology
Published: November 17, 2025
Novel Homozygous Variants in CIDEC and WRN in a Young Female with Lipodystrophy and Thyroid Cancer.
Journal: International journal of molecular sciences
Published: November 17, 2025
Last Updated: 06/30/2026