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Research 301–330 of 320
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Autophagy-Mediated Cellular Remodeling during Terminal Differentiation of Keratinocytes in the Epidermis and Skin Appendages
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Off-Label Use of Botulinum Toxin in Dermatology—Current State of the Art
- Acrodermatitis enteropathica in the pediatric population: a literature review of real-world studies
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- Cannabinoid Compounds as a Pharmacotherapeutic Option for the Treatment of Non-Cancer Skin Diseases
- Hair microscopy: an easy adjunct to diagnosis of systemic diseases in children
- Updated strategies for the management, pathogenesis and molecular genetics of different forms of ichthyosis syndromes with prominent hair abnormalities
- Lrig1 Expression in Human Sebaceous Gland Tumors
- Zebrafish Model of Hereditary Pigmentary Disorders
- Hypothesis: platelet-rich plasma as an adjunct therapy for eczema targeting inflammation, skin barrier repair, and chronic recurrence
- Melanocytes in regenerative medicine applications and disease modeling
- Giant solitary trichoepithelioma: A rare trichogenic tumor
- Minoxidil oral en alopecias no androgénicas
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Use of Contact Immunotherapy in the Treatment of Skin Diseases Other than Alopecia Areata
- Subject Index
- Hidradenitis Suppurativa and Comorbid Disorder Biomarkers, Druggable Genes, New Drugs and Drug Repurposing—A Molecular Meta-Analysis
- Intercellular junctions in normal epidermis
- Molecular Genetics of the PI3K-AKT-mTOR Pathway in Genodermatoses: Diagnostic Implications and Treatment Opportunities
- Di-Genic Inheritance in Genodermatoses: Insights from Two Consanguineous Cases in a Reference Lebanese Center within the Middle East and North Africa (MENA) Region
- Unveiling the Roots of Monogenic Genodermatoses: Genotrichoses as a Paradigm
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Corneodesmosomes and corneodesmosin: from the stratum corneum cohesion to the pathophysiology of genodermatoses
- Botulinum Toxin Off-Label Use in Dermatology: A Review
- Harnessing neuroendocrine controls of keratin expression: A new therapeutic strategy for skin diseases?
- Overexpression of human keratin 16 produces a distinct skin phenotype in transgenic mouse skin
- Spectrum of skin diseases in Yemen (Hajjah and adjacent region)
- Male fertility and skin diseases