Novel Heterozygous LMNA Variants Causing Familial Partial Lipodystrophy, Dunnigan Variety

por Wadhwa, Akhilesh, Vasandani, Chandna, Garg, Abhimanyu
Publicado 2021

SUN-135 Dual Energy X-Ray Absorptiometry (DEXA) as a Diagnostic Tool for Familial Partial Lipodystrophy, Dunnigan Variety (FPLD2)

por Vasandani, Chandna, Li, Xilong, Adams Huet, Beverly, Garg, Abhimanyu
Publicado 2019

SUN-LB111 Comparison of Phenotype and Metabolic Abnormalities Among Familial Partial Lipodystrophy Due to LMNA or PPARG Variants

por Vasandani, Chandna, Li, Xilong, Sekizkardes, Hilal, Brown, Rebecca, Garg, Abhimanyu
Publicado 2020

Phenotypic Differences Among Familial Partial Lipodystrophy Due to LMNA or PPARG Variants

por Vasandani, Chandna, Li, Xilong, Sekizkardes, Hilal, Brown, Rebecca J, Garg, Abhimanyu
Publicado 2022

Very Severe Hypertriglyceridemia in a Large US County Health Care System: Associated Conditions and Management

por Esparza, Maria Isabel, Li, Xilong, Adams-Huet, Beverley, Vasandani, Chandna, Vora, Amy, Das, Sandeep R, Garg, Abhimanyu, Ahmad, Zahid
Publicado 2019