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Research 331–360 of 1000+
- T Cell Immunodeficiency, Congenital Alopecia, and Nail Dystrophy
- Making the head: Caspases in life and death
- Disorders of Keratinization
- Cutaneous transcriptome analysis in NIH hairless mice
- Percutaneous Absorption of Minoxidil in Man
- Cutaneous manifestations of metabolic diseases: uncommon presentations
- Unveiling the Potential of Dermoscopy in Diagnosing Netherton Syndrome
- Clinical and epidemiological characteristics and hormonal profile of adult females with acne vulgaris: a cross-sectional study from a tertiary care hospital
- 115 AE法による実機水車発電機軸受の診断(セッション4 評価・診断II)
- Impaired Lef1 activation accelerates iPSC-derived keratinocytes differentiation in Hutchinson-Gilford Progeria Syndrome
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Color Doppler Ultrasound Pattern of Cutaneous Exosomes at High and Ultra-High Frequency.
- Atrichia with papular lesions mimicking alopecia areata universalis
- Endocrinopathies, Atypical
- Dermatoscopy: Alternative uses in daily clinical practice
- Nutrition and hair
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Alternative uses of dermoscopy in daily clinical practice: An update
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Aplasia cutis congenita on lumbosacral area
- Letters to Dermatology
- Dermatological Manifestations in Pediatric Patients with Chronic Kidney Disease.
- Lesions in the Axilla After Hair Removal Using Intense Pulsed Light
- Disturbed Keratinocyte Differentiation in Transgenic Mice and Organotypic Keratinocyte Cultures as a Result of Spermidine/Spermine N1-Acetyltransferase Overexpression
- Cutaneous Findings and Systemic Associations in Women With Polycystic Ovary Syndrome
- The development of several organs and appendages is impaired in mice lacking Sp6
- The use of dihydroxyacetone for photoprotection in variegate porphyria
- Australasian Society for Dermatology Research Meeting, May 2006
- The Shaven (Sha) Mutation, Chromosome 15
- Furnishing Wound Repair by the Subcutaneous Fascia