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Research 61–90 of 1000+
- Improvement of Skin Lesions in an Adult with CHILD Syndrome Treated with 2% Ketoconazole Cream
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Biological significance of FoxN1 gain-of-function mutations during T and B lymphopoiesis in juvenile mice
- Symmetrical acrokeratoderma: A peculiar entity in China? Clinicopathologic and immunopathologic study of 34 new cases
- Banding Pattern on Polarized Hair Microscopic Examination and Unilateral Polymicrogyria in a Patient With Steroid Sulfatase Deficiency
- Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Dermatopathology and molecular genetics
- New clinico‐genetic classification of trichothiodystrophy
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- Steatocystoma Multiplex
- ST14 interacts with TMEFF1 and is a predictor of poor prognosis in ovarian cancer
- Adipocytes in Skin Health and Disease
- Steroid Sulfatase in the Human Hair Follicle Concentrates in the Dermal Papilla
- Vitamin D and skin diseases: A review
- Madarosis: A marker of many Maladies
- Genetic Hair Disorders: A Review
- A Monoallelic Two-Hit Mechanism in PLCD1 Explains the Genetic Pathogenesis of Hereditary Trichilemmal Cyst Formation
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- Lysine Carboxymethyl Cysteinate (LCC) Protects the Epidermis from UVB-Induced Barrier Damage Through the Activation of Autophagy
- Inflammatory Vegetative Lesions of the Perineum: A Rare and Severe Clinical Presentation of Netherton Syndrome
- Montagna Symposium 2017—Precision Dermatology: Next Generation Prevention, Diagnosis, and Treatment
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- The oestrogen receptor 2 (<i>ESR2</i>) gene in female-pattern hair loss: replication of association with rs10137185 in German patients
- Netherton Syndrome in a 9-Month-Old Child: Unraveling a Complex Dermatologic Disorder
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Disorders of hair in children
- DERMATOLOGIC DISEASES AND PROBLEMS OF WOMEN THROUGHOUT THE LIFE CYCLE
- Cushing Syndrome from Percutaneous Absorption of 1% Hydrocortisone Ointment in Netherton Syndrome