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Research 211–240 of 1000+
- Collagen Involvement in Health, Disease, and Medicine
- Case Report: A novel KRT74 variant in an eight-year-old boy with alopecia totalis successfully treated with baricitinib
- Recently Identified Forms of Epidermolysis Bullosa
- Loose anagen hair syndrome
- Asebia-2J (Scd1ab2J): A New Allele and a Model for Scarring Alopecia
- The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs
- Genetic Variant of the Canine FGF5 Gene for the Hair Length Trait in the Akita: Utility for Hair Coat Variations and Welfare in Conservation Breeding
- Role of caffeine in the management of androgenetic alopecia
- Skin Sceneries of Thyroid Disorders and Impact of Thyroid on Different Skin Diseases: A Scoping Review Focused on Pediatric Patients
- Sphingolipid metabolism orchestrates establishment of the hair follicle stem cell compartment
- Oral Presentations
- Loose Anagen Hair Syndrome in Black‐Haired Indian Children
- Premature Hair Graying: Underlying Contributors and Management Approaches - An Updated Literature Review
- Premature graying of hair
- HAIR REGROWTH
- Two mouse mutations mapped to chromosome 11 with differing morphologies but similar progressive inflammatory alopecia
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- A Case of Familial Male-limited Precocious Puberty with a Novel Mutation
- Progeroide Syndrome
- Biotin
- Central centrifugal cicatricial alopecia: a subtype of lichen planopilaris in African descent?
- Diabetes, ovarian tumor, hyperparathyroidism, and papillary cancer: A chance association?
- SELF-CARE OF MALE PATTERN HAIR LOSS – Selfcare Journal
- Caring for women with polycystic ovary syndrome
- Why are men with premature alopecia at higher risk of benign prostatic hyperplasia? And what about prostate cancer?
- Anagen effluvium
- DERMATOLOGIC DISEASES AND PROBLEMS OF WOMEN THROUGHOUT THE LIFE CYCLE
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- The clinical spectrum of parathyroid disease