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Research 31–60 of 199
- Endocrine-skin interactions
- The Hirsute Woman: Challenges in Evaluation and Management
- Dermatologic manifestations of endocrine disorders
- Evidence-based approach to cutaneous hyperandrogenism in women
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- Premature aging syndromes: From patients to mechanism
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Skin, a mirror reflecting diabetes mellitus: A longitudinal study in a tertiary care hospital in Gujarat
- Dermatologic manifestations of endocrine disorders
- High-throughput Sequencing to Identify Monogenic Etiologies in a Preselected Polycystic Ovary Syndrome Cohort
- Pseudo-Cushing Syndrome
- Pathogenesis and causes of hirsutism
- Parry–Romberg Syndrome: Radioclinical Dissociation in a Paucisymptomatic Form and a Proposed Diagnostic Framework
- Approach to the Patient: Diagnostic Challenges in the Work Up for Polycystic Ovary Syndrome
- Rare and Underappreciated Causes of Polycystic Ovarian Syndrome
- Neuroimaging of sleep and depression
- Unravelling the link between insulin resistance and androgen excess
- Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome
- Dyslipidaemia in women with polycystic ovary syndrome referred to a teaching hospital in Cape Town, South Africa
- Topical imiquimod—Be aware of the unexpected
- 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
- Cutaneous drug reactions
- Genetics and Epigenetics of Polycystic Ovary Syndrome
- The evaluation of endothelial function with flow-mediated dilatation and carotid intima media thickness in young nonobese polycystic ovary syndrom patients; existence of insulin resistance alone may not represent an adequate condition for deterioration of endothelial function
- 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
- Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin
- Inherited Disorders of the Hair
- Prevalence of the metabolic syndrome in African populations: A systematic review and meta-analysis
- Impaired LEF1 Activation Accelerates iPSC-Derived Keratinocytes Differentiation in Hutchinson-Gilford Progeria Syndrome
- Skin alterations as possible clinical markers of diabetes mellitus and metabolic syndrome