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Safety and effectiveness in an uncontrolled setting of glucagon-like-peptide-1 receptor agonists in patients with familial partial lipodystrophy: Real-life experience from a national reference network.
Not available
S-EPMC11885082
|
biostudies-literature
Cite
Lipodystrophic syndromes due to LMNA mutations: recent developments on biomolecular aspects, pathophysiological hypotheses and therapeutic perspectives.
Not available
S-EPMC5973242
|
biostudies-literature
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A Novel Lamin A Mutant Responsible for Congenital Muscular Dystrophy Causes Distinct Abnormalities of the Cell Nucleus.
Not available
S-EPMC5268432
|
biostudies-literature
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Progerin Expression Induces Inflammation, Oxidative Stress and Senescence in Human Coronary Endothelial Cells.
Not available
S-EPMC7290406
|
biostudies-literature
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LMNA mutations induce a non-inflammatory fibrosis and a brown fat-like dystrophy of enlarged cervical adipose tissue.
Not available
S-EPMC3204020
|
biostudies-literature
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Two Decades after Mandibuloacral Dysplasia Discovery: Additional Cases and Comprehensive View of Disease Characteristics.
Not available
S-EPMC8535562
|
biostudies-literature
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Laminopathies' Treatments Systematic Review: A Contribution Towards a 'Treatabolome'.
Not available
S-EPMC8203247
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biostudies-literature
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Diagnosis, risk factors and management of diabetes mellitus in HIV-infected persons in France: A real-life setting study.
Not available
S-EPMC8121550
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biostudies-literature
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Extracellular matrix remodeling and transforming growth factor-β signaling abnormalities induced by lamin A/C variants that cause lipodystrophy.
Not available
S-EPMC5234718
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biostudies-literature
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Ciliopathies are responsible for short stature and insulin resistance: A systematic review of this clinical association regarding SOFT syndrome.
Not available
S-EPMC11470920
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biostudies-literature
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