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Research 181–210 of 1000+
- A polarizing light microscopy can be an easy and reliable diagnostic tool of congenital keratinizing disorders including Netherton syndrome
- Netherton Syndrome – Responding to Oral Retinoids
- Disorders of Keratinization
- Keratin gene mutations in disorders of human skin and its appendages
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Rickets in association with skin diseases and conditions: A review with emphasis on screening and prevention
- Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Efficient In Vitro Transfection of Human Keratinocytes with an Adenovirus-Enhanced Receptor-Mediated System
- Skin, Genetic Defects, and Aging
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Unveiling the Potential of Dermoscopy in Diagnosing Netherton Syndrome
- Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions
- Inflammatory Vegetative Lesions of the Perineum: A Rare and Severe Clinical Presentation of Netherton Syndrome
- Cushing Syndrome from Percutaneous Absorption of 1% Hydrocortisone Ointment in Netherton Syndrome
- 9. Immunology and Genetics
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- The oestrogen receptor 2 (<i>ESR2</i>) gene in female-pattern hair loss: replication of association with rs10137185 in German patients
- Montagna Symposium 2017—Precision Dermatology: Next Generation Prevention, Diagnosis, and Treatment
- Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disability
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
- Netherton Syndrome in a 9-Month-Old Child: Unraveling a Complex Dermatologic Disorder
- Ischemic onycholysis of the hands
- Site of beige (<i>bg</i>) and leaden (<i>ln</i>) pigment gene expression determined by recombinant embryonic skin grafts and aggregation mouse chimaeras employing sash (<i>W</i><sup><i>sh</i></sup>) homozygotes
- Rare clinical features of the Ellis van Creveld syndrome: A case report and literature review
- Why are men with premature alopecia at higher risk of benign prostatic hyperplasia? And what about prostate cancer?
- Early skin biopsy is helpful for the diagnosis and management of neonatal and infantile erythrodermas
- Crystalline Cataract and Uncombable Hair
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- Fatty acids and related lipid mediators in the regulation of cutaneous inflammation