Last Updated: 09/26/2026
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Found 48 publications
Left Atrial Myxoma Presenting As Multiple Embolic Strokes in a Young Female: A Case Report.
Journal: Cureus
Published: December 05, 2025
A recurrent ACAA2 variant causes a dominant syndrome of lipodystrophy, lipomatosis, infantile steatohepatitis, and hypoglycemia.
Journal: The Journal of clinical investigation
Published: November 04, 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
Phospholipid biosynthetic pathways and lipodystrophies: a novel syndrome due to PLAAT3 deficiency.
Journal: Nature reviews. Endocrinology
Published: January 08, 2024
Early-onset diabetes mellitus as a presenting feature of Werner's syndrome in an Indian family.
Journal: Molecular genetics & genomic medicine
Published: June 07, 2023
Regulated adipose tissue-specific expression of human AGPAT2 in lipodystrophic Agpat2-null mice results in regeneration of adipose tissue.
Journal: iScience
Published: February 21, 2023
Bowen's disease of the palm: a cautionary tale.
Journal: British journal of hospital medicine (London, England : 2005)
Published: August 08, 2022
Face-sparing Congenital Generalized Lipodystrophy Type 1 Associated With Nonclassical Congenital Adrenal Hyperplasia.
Journal: The Journal of clinical endocrinology and metabolism
Published: March 17, 2022
Autoantibodies to Perilipin-1 Define a Subset of Acquired Generalized Lipodystrophy.
Journal: Diabetes
Published: January 03, 2022
Last Updated: 09/26/2026