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Research 151–180 of 1000+
- Diagnostic criteria for PCOS: Is there a need for a rethink?
- Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis.
- Case report: Two individuals with AEBP1-related classical-like EDS: Further clinical characterisation and description of novel AEBP1 variants
- PO:17:252 | The choice between belimumab and anifrolumab: analysis of a monocentric cohort
- POLİKİSTİK OVER SENDROMU'NUN ALT GRUPLARINDA METABOLİK ÖZELLİKLER
- 303 The role of rare variants in male-pattern hair loss: Analysis of whole exome sequencing data in the UK Biobank
- Treatment Strategies for Cutaneous and Oral Mucosal Side Effects of Oncological Treatment in Breast Cancer: A Comprehensive Review
- Trichoscopy of aplasia cutis congenita of the scalp in skin of color
- Report on the 11th National Congress AICPE (Associazione Italiana di Chirurgia Plastica Estetica) Held in Rimini, Italy, 12–14 April 2024
- Dermoscopic spectrum of rosacea
- Abstracts
- Platelet-Rich Plasma: New Performance Understandings and Therapeutic Considerations in 2020
- Autoimmune Polyglandular Syndrome Type 1 in Russian Patients: Clinical Variants and Autoimmune Regulator Mutations
- Update on hidradenitis suppurativa: connecting the tracts
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- Modulation of Macrophage Function by Bioactive Wound Dressings with an Emphasis on Extracellular Matrix-Based Scaffolds and Nanofibrous Composites
- N6-methyladenosine RNA Methylation Correlates with Immune Microenvironment and Immunotherapy Response of Melanoma
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis
- Phenotypic heterogeneity in human genetic diseases: ultrasensitivity-mediated threshold effects as a unifying molecular mechanism
- The hairless (hr) gene is involved in the congential hypotrichosis of Valle del Belice sheep
- Author response: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Peer Review #2 of "Computational drug repositioning based on side-effects mined from social media (v0.2)"
- Actinic keratosis: a clinical and epidemiological revision
- New developments in occupational dermatology
- Cold Plasma An emerging technology for clinical use in wound healing
- Dissecting Cellulitis of the Scalp: Linking Pathogenesis to Therapy
- Induction of basal cell carcinomas and trichoepitheliomas in mice overexpressing GLI-1
- Stimulation of ectodermal organ development by Ectodysplasin-A1
- Shh maintains dermal papilla identity and hair morphogenesis via a Noggin–Shh regulatory loop