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Research 871–900 of 1000+
- Alopecia Areata and Habit Tic Deformities
- Short Anagen Syndrome in an Indian Woman with its Impact on Quality-of-Life
- Advances in the genetic understanding of hypohidrotic ectodermal dysplasia
- “Shedding” low yield testing for telogen effluvium: A cross-sectional study of 16,381 laboratory results from newly diagnosed patients
- Contents
- IgG/IgA pemphigus with differing regional presentations
- Pigmentary mosaicism: An update
- Wwox Deficiency Causes Downregulation of Prosurvival ERK Signaling and Abnormal Homeostatic Responses in Mouse Skin
- [Regression analysis of serum bone metabolic markers and traditional Chinese medicine syndromes in patients with CKD-MBD].
- Defective trophoblast function in mice with a targeted mutation of Ets2
- <i>WNT10A</i> , dermatology and dentistry
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotype
- Becker's nevus associated with chromosomal mosaicism and congenital adrenal hyperplasia
- Influence of Dosing Time on the Efficacy and Safety of Finasteride in Rats
- Autophagy-Mediated Cellular Remodeling during Terminal Differentiation of Keratinocytes in the Epidermis and Skin Appendages
- Oil in a Commercial Standard Diet Needs Its Product Specifications
- Ring-shaped Alopecia on the Scalp in a 3-month-old Infant
- PA05 A rare case of cardiocutaneous syndrome in a young child
- Clinical Corner: Case Report Spermatozoa and Chronic Treatment with Finasteride: A TEM and FISH Study
- THE LOS ANGELES DERMATOLOGICAL SOCIETY
- Bimatoprost solution 0·03% topical application to the eyelid margin for the treatment of eyelash hypotrichosis
- Skin manifestations of celiac disease
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Associated Variables of Myositis in Systemic Lupus Erythematosus: A Cross-Sectional Study
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- P‐41 Psychogenic alopecia by fur‐plucking in a family of seal‐point Siamese cats: three cases
- Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion