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Research 151–180 of 1000+
- Vitiligo and alopecia areata: apples and oranges?
- Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness
- Defects in Androgen Biosynthesis Causing 46,XY Disorders of Sexual Development
- METHOTREXATE FOR GENERALIZED PUSTULAR PSORIASIS IN A 2-YEAR-OLD CHILD
- Hypoparathyroidism as the single major component for decades of autoimmune polyglandular syndrome type 1
- Human Skin Aging: Physiology and Pathophysiology
- Deep Hair Phenomics: Implications in Endocrinology, Development, and Aging
- COMPREHENSIVE OVERVIEW ON THE PROBLEMS OF HAIR AND THE VARIOUS HERBAL APPROACHES TO TREAT THEM
- Genes of Congenital Dermatologic Disorders in Dogs—A Review
- Alopecia Areata: literature review
- ALOPECIA AREATA IN INFANTS: IS IT UNCOMMON?
- Polycystic ovary syndrome
- HAIR MATRIX CELL KINETICS: A SELECTIVE REVIEW
- Alopecia and the Aging Male
- LB918 Analysis of National Inpatient Sample to characterize admissions for pediatric patients with dystrophic epidermolysis bullosa
- What Is the Male Polycystic Ovary Syndrome Phenotype?
- British Society for Paediatric Dermatology Annual Meeting, Sheffield, 18-19 November 2016
- Multiorgan Dysfunction in a 7-Month-Old Boy With Developmental Delay and Poor Growth
- Hidradenitis suppurativa: pathogenesis and management
- Origin, Clinical Presentation, and Diagnosis of Facial Hypermelanoses
- The role of keratin proteins and their genes in the growth, structure and properties of hair
- Generalized Vitiligo Associated Autoimmune Diseases in Japanese Patients Their Families
- Handbook of Mouse Mutations with Skin and Hair Abnormalities: Animal Models and Biomedical Tools
- Male fertility and skin diseases
- Gut instinct: Using tofacitinib to treat alopecia areata in the context of comorbid inflammatory bowel disease
- Alopecia Areata in Skin of Color Patients: New Considerations Sparked by the Approval of Baricitinib
- Aging Skin: A Window to the Body
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Genetic Disorders and Defects in Vitamin D Action
- Hidradenitis Suppurativa as a Potential Subtype of Autoinflammatory Keratinization Disease