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Research 391–420 of 784
- Kallmann's syndrome: skeletal and psychological aspects of late diagnosis.
- CUTANEOUS T-CELL LYMPHOMA WITH LYMPH NODE METASTASIS IN AN ADULT ADDAX (<i>ADDAX NASOMACULATUS</i>)
- Bee venom: a case of effectiveness on skin varicosities veins with review of its dermatological benefits
- Overlap Between Ulerythema Ophryogenes and Keratosis Follicularis Spinulosa Decalvans: a Case Report
- Tatalaksana Tinea Favosa pada Anak Usia 7 Tahun di RSUD dr. Fauziah Bireuen
- S4890 Infliximab-Induced Synovitis, Acne, Pustulosis, Hyperostosis, Osteitis Syndrome
- BH02 Overcoming genetic drivers in alopecia areata: hair regrowth in a patient with the <i>AIRE</i> gene mutation treated with ruxolitinib
- Enigma of Folliculitis Decalvans in Two Pediatric Sisters, Treated with Low-Dose Isotretinoin and Erythromycin
- Ayurvedic management of systemic sclerosis - A case report
- Successfully Nonsurgical Epidermoid Cyst Management with Recombinant Hydrolytic Enzymes: A Case Report
- A case of myasthenia gravis following alopecia areata
- BLACK PIEDRA. CLINICAL CASE
- Uncombable hair improved by biotin
- Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1
- Case Report: 7 Year-Old Saudi Female with Monilethrix
- Hair in the Wrong Place
- KRASG12D mutant cells are outcompeted by wild type neighbours in adult pancreas in an EPHA2-dependent manner
- GENOTYPE ? PHENOTYPE CORRELATIONS IN CUTANEOUS MELANOMA PATIENTS CARRIER OF THE MITF p.E318K PATHOGENIC VARIANT
- And next… Adnexa: Frontal Fibrosing Alopecia
- A case report and brief literature review of Klippel-Trénaunay syndrome
- Cytokine profiling of alopecia areata phenotypic subsets
- Commentary 2
- Index of Suspicion
- JAK inhibitors in dermatology: The promise of a new drug class
- Hair follicle dermal cells differentiate into adipogenic and osteogenic lineages
- Patched1 Functions as a Gatekeeper by Promoting Cell Cycle Progression
- GLI2 Is Expressed in Normal Human Epidermis and BCC and Induces GLI1 Expression by Binding to its Promoter
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Ornithine decarboxylase is a target for chemoprevention of basal and squamous cell carcinomas in Ptch1+/– mice