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- How to diagnose a lipodystrophy syndrome
- Biological Features Implies Potential Use of Autologous Adipose-Derived Stem/Progenitor Cells in Wound Repair and Regenerations for the Patients with Lipodystrophy
- A 10 Mb duplication in chromosome band 5q31.3–5q33.1 associated with late-onset lipodystrophy, ichthyosis, epilepsy and glomerulonephritis
- Impact of Combined Baricitinib and FTI Treatment on Adipogenesis in Hutchinson–Gilford Progeria Syndrome and Other Lipodystrophic Laminopathies
- Treatment of Lipodystrophy with Troglitazone
- Loss of adipocyte phospholipase gene PLAAT3 causes lipodystrophy and insulin resistance due to inactivated arachidonic acid-mediated PPARγ signaling
- Dunnigan-Type Familial Partial Lipodystrophy: Understanding and Treating the Syndrome
- Centrifugal lipodystrophy of the scalp manifesting as centrifugal lipodystrophic alopecia
- 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
- MON-194 A Case Of Sertoli Cell Tumor In A Patient With Familial Partial Lipodystrophy Type 2
- 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
- Anterior neck fat deposition in lipodystrophy syndrome; a new variant on a theme?
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- Peroxisome proliferator-activated receptors (PPARs) and PPAR agonists: the ‘future’ in dermatology therapeutics?
- Adverse Drug Reactions in HIV/AIDS Patients on Highly Active Antiretro Viral Therapy: A Review of Prevalence
- The metabolic syndrome- associated small G protein ARL15 plays a role in adipocyte differentiation and adiponectin secretion
- Tissue fibrosis associated depletion of lipid‐filled cells
- Restoring neuropetide Y levels in the hypothalamus ameliorates premature aging phenotype in mice
- Hutchinson-Gilford progeria syndrome: Report of 2 cases and a novel LMNA mutation of HGPS in China
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- Progeria (Hutchinson-Gilford Syndrome): Literature Review and Clinical Case
- Author response: Human biallelic MFN2 mutations induce mitochondrial dysfunction, upper body adipose hyperplasia, and suppression of leptin expression
- The transcription elongation factors Spt4 and Spt6 promote dermal adipocyte differentiation
- 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
- Skin disorders in diabetes mellitus
- Syndromes of Severe Insulin Resistance (SSIRs)
- Diabetes and Skin — A Review
- Treatment of acne with intermittent isotretinoin, cohort study
- Fibrodysplasia Ossificans Progressiva (FOP): A Segmental Progeroid Syndrome