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1 ensaios clínicos encontrados.
A Novel PPARG R212W Variant Causes Familial Partial Lipodystrophy Type 3: Clinical Presentation and Functional Characterization.
Familial Generalized and Partial Lipodystrophies Due to Rare Biallelic Variants in LMNA.
Increased epicardial adipose tissue is part of the phenotype of LMNA-associated partial lipodystrophy and could contribute to increased cardiovascular risk.
Novel Homozygous Variants in CIDEC and WRN in a Young Female with Lipodystrophy and Thyroid Cancer.
Improvement of severe hypertriglyceridemia in atypical subtype 4 partial lipodystrophy with volanesorsen.