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Research 31–60 of 1000+
- LB918 Analysis of National Inpatient Sample to characterize admissions for pediatric patients with dystrophic epidermolysis bullosa
- CRISPR/Cas9-mediated Generation of<i>COL7A1</i>-deficient Keratinocyte Model of Recessive Dystrophic Epidermolysis Bullosa
- Abstracts
- Rothmund‐Thomson syndrome type 2 – a rare cause of chronic wounds
- Unveiling the Roots of Monogenic Genodermatoses: Genotrichoses as a Paradigm
- The Role of Cytochrome P-450 in Dermatology
- Pseudofolliculitis barbae; current treatment options
- Trichoscopy
- Eyebrow Loss
- CURRENT UNDERSTANDING OF VITILIGO: A COMPREHENSIVE LITERATURE REVIEW
- Clinical report of a Holstein's calf with ichthyosis.
- The Psychology of Gray Hair
- Does Complement Have a Role in the Pathogenesis of Alopecia Areata?
- The cat with alopecia
- 4th Intercontinental Meeting of Hair Research Societies 2004 The "World of Hair"
- Two Incidental Sibling Diagnoses of Netherton Syndrome in Separate Visits: A Case Report
- Androgen Receptor Polymorphisms (CAG Repeat Lengths) in Androgenetic Alopecia, Hirsutism, and Acne
- Retinoids Putting the “A” in Alopecia
- Missense mutation Y449H of the K10 gene in a patient with severe epidermolytic ichthyosis
- Fatty acid oxidation fuels mitochondrial respiration to drive epidermal stem cell fate and differentiation
- Frontal Fibrosing Alopecia – a review and a practical guide for clinicians
- 1360 Regulation of bmp signalling in melanogenesis, pigment transfer and melanocyte migration
- Clinical Findings, Cutaneous Pathology, and Response to Therapy in 21 Patients With Keratosis Pilaris Atrophicans
- Alopecia areata: What’s new in epidemiology, pathogenesis, diagnosis, and therapeutic options?
- Symmetrical alopecia in the dog
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- Inherited Disorders of Corneocyte Proteins
- Transcriptomic crossroads: Decoding genes and pathways that connect alopecia areata with chronic inflammatory skin disorders
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Genetics of Structural Hair Disorders