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Research 631–660 of 1000+
- Cutaneous manifestations of polycystic ovary syndrome: A cross-sectional clinical study
- Tumour Necrosis Factor Alpha, Interferon Gamma and Substance P Are Novel Modulators of Extrapituitary Prolactin Expression in Human Skin
- What causes acne inversa (or hidradenitis suppurativa)? – the debate continues
- Pseudofolliculitis barbae; current treatment options
- Phytochemistry and pharmacological studies of Plumbago zeylanica L.: a medicinal plant review
- Dermoscopy of skin infestations and infections (entomodermoscopy) – Part I: dermatozoonoses and bacterial infections
- Pili annulati with fragility: Electron microscopic findings of a case
- Madarosis from mitochondriopathy
- Overexpression of hypoxia-inducible factor-1α in hidradenitis suppurativa: the link between deviated immunity and metabolism
- Advances in molecular pathogenesis of hidradenitis suppurativa: Dysregulated keratins and ECM signaling
- What causes acne inversa (or hidradenitis suppurativa)? – The debate continues
- Clinical and Dermoscopic Approaches to Diagnosis of Frontal Fibrosing Alopecia: Results From a Multicenter Study of the International Dermoscopy Society
- Unusual Case Presentation of Systemic Lupus Erythematosus in a Young Woman
- Cardiovascular risk markers in premature canities
- Mycosis Fungoides in Elderly Adults—A Diagnostic Challenge
- The Use of Robotic Systems in Aesthetic/Cosmetic Plastic Surgery—A Review
- Clinical dermatoendocrinology: saving lives by looking at the skin.
- An Unusual Case of Mycosis Fungoides Presenting with Multiple Atypical Morphologies in a Photoexacerbated Distribution
- Clinical and demographic characteristics of frontal fibrosing alopecia in a dermatology referral center in Bogota, Colombia: a descriptive cross-sectional study
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- Clinicopathologic Case 2: Multiple Intraoral White Lesions in a 55-year-old Female
- Multisystemic eosinophilic epitheliotropic disease in a horse
- A(1-7) reduces pathologies associated with SLE in MRL-<i>lpr</i> mice
- Monilethrix – Case report of a rare disease
- The JAK/STAT signaling pathway: from bench to clinic
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Physiological Regeneration of Skin Appendages and Implications for Regenerative Medicine
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Intense Pulsed Light: From the Past to the Future