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Research 541–570 of 1000+
- Diseases of Periocular Hair
- Diagnostic Exercise: Severe Bilaterally Symmetrical Alopecia in a Horse
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Topical Treatment of Eyebrow Hypotrichosis with Bimatoprost 0.03% Solution: Case Report and Literature Review
- Skin Diseases in Horses
- Sebaceous carcinoma arising at a chronic candidiasis skin lesion of a patient with keratitis-ichthyosis-deafness (KID) syndrome
- Deciphering the Mesodermal Potency of Porcine Skin-Derived Progenitors (SKP) by Microarray Analysis
- Acquired Uncombable Hair
- Disorders of hair
- Heterogeneity of Polymorphous Light Eruption: A Study of 105 Patients
- The spectrum of nephrocutaneous diseases and associations
- Infertility: Evaluation and Initial Management
- Hair loss and its management in children
- Significance of iron status in hair loss in women
- Darier Sign: A Historical Note
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- An animal study on the effectiveness of platelet-rich plasma as a direct pulp capping agent
- Cronkhite-Canada Syndrome: A Case Report
- Ectodysplasin-A2 induces dickkopf 1 expression in human balding dermal papilla cells overexpressing the ectodysplasin A2 receptor
- Identification of differentially expressed genes in actinic keratosis samples treated with ingenol mebutate gel
- A Case Report of Werner’s Syndrome With a Novel Mutation From India
- 1310 Anti-aging effects of retinoid hydroxypinacolone retinoate on skin models
- Botanicals With Dermatologic Properties Derived From First Nations Healing: Part 1—Trees
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Glycolytic Dysfunction in Granulosa Cells and Its Contribution to Metabolic Dysfunction in Polycystic Ovary Syndrome
- Hypothyroidism in Dogs
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- THE PEDIATRICIAN AND THE SEXUALLY ACTIVE ADOLESCENT
- Keratosis pilaris atrophicans faciei: An observational, descriptive, retrospective clinical study
- The urine as a diagnostic key for a homozygous EGFR mutation