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Maria Cristina Foss de Freitas

University of Michigan

12

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2

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Body Composition And Bone Mineral Differences According to Lamin A (LMNA) Genotype in Familial Partial Lipodystrophy Type 2

2021 Journal of the Endocrine Society
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The Long-Term Safety and Efficacy of Metreleptin in Various Forms of Partial Lipodystrophy

2021 Journal of the Endocrine Society
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Untangling the Heterogeneity of Acquired Generalized Lipodystrophy

2021 Journal of the Endocrine Society
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Inhibition of Angiopoietin-Like 3 (ANGPTL3) Reduces Adipose Tissue Insulin Resistance in Patients With Familial Partial Lipodystrophy

2021 Journal of the Endocrine Society
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Abnormal Non Esterified Fatty Acid Suppression After a Mixed Meal Test in Patients With Partial Lipodystrophy

2021 Journal of the Endocrine Society
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Adipocyte-specific deletion of lamin A/C largely models human familial partial lipodystrophy type 2.

2021 Diabetes
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SAT-617 Potential Utility of the Mixed Meal Test for Differential Diagnosis of Partial Lipodystrophy from Common Type 2 Diabetes and Truncal Obesity

2020 Journal of the Endocrine Society
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OR17-02 Changes in Hepatokines and Apolipoproteins Are Associated with Metabolic Response to Metreleptin in Partial Lipodystrophy

2020 Journal of the Endocrine Society
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SAT-622 Heterogeneity of Familial Partial Lipodystrophy Type 2 from a Genotype-Phenotype Perspective

2020 Journal of the Endocrine Society
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MON-121 Pain Is a Major Driver of Quality of Life and Psychoemotional Health in Lipodystrophy Syndromes

2020 Journal of the Endocrine Society
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