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- Treatment of Lipodystrophy with Troglitazone
- Dunnigan-Type Familial Partial Lipodystrophy: Understanding and Treating the Syndrome
- Fibrodysplasia Ossificans Progressiva (FOP): A Segmental Progeroid Syndrome
- Anterior neck fat deposition in lipodystrophy syndrome; a new variant on a theme?
- How to diagnose a lipodystrophy syndrome
- New Insight for Enhanced Topical Targeting of Caffeine for Effective Cellulite Treatment: In Vitro Characterization, Permeation Studies, and Histological Evaluation in Rats
- Hypersensitivity reactions to anticoagulant drugs: diagnosis and management options
- Kojyl Cinnamate Ester Derivatives Increase Adiponectin Expression and Stimulate Adiponectin-Induced Hair Growth Factors in Human Dermal Papilla Cells
- Metreleptin Treatment in a Boy with Congenital Generalized Lipodystrophy due to Homozygous c.465_468delGACT (p.T156Rfs*8) Mutation in the BSCL2 Gene: Results From the First-year
- Biological Features Implies Potential Use of Autologous Adipose-Derived Stem/Progenitor Cells in Wound Repair and Regenerations for the Patients with Lipodystrophy
- Impact of Combined Baricitinib and FTI Treatment on Adipogenesis in Hutchinson–Gilford Progeria Syndrome and Other Lipodystrophic Laminopathies
- The metabolic syndrome- associated small G protein ARL15 plays a role in adipocyte differentiation and adiponectin secretion
- Progressive Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD) from a Young Age Due to a Rare Genetic Disorder, Familial Partial Lipodystrophy: A Case Report and Review of the Literature
- Restoring neuropetide Y levels in the hypothalamus ameliorates premature aging phenotype in mice
- Progeria (Hutchinson-Gilford Syndrome): Literature Review and Clinical Case
- Syndromes of Severe Insulin Resistance (SSIRs)
- Viewpoint 7
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- Tissue fibrosis associated depletion of lipid‐filled cells
- Author response: Human biallelic MFN2 mutations induce mitochondrial dysfunction, upper body adipose hyperplasia, and suppression of leptin expression
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- Decision letter: Human biallelic MFN2 mutations induce mitochondrial dysfunction, upper body adipose hyperplasia, and suppression of leptin expression
- Hypersensitivity Reactions to Anticoagulant Drugs
- Animals in Dermatology
- Radiesse
- Adipocytes in Skin Health and Disease
- Skin and metabolic syndrome: A review of the possible associations
- Maternal PPARγ protects nursing neonates by suppressing the production of inflammatory milk
- Endocrine-skin interactions
- A guide to studying human dermal adipocytes in situ