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Research 61–90 of 1000+
- Gene therapy for alopecia in type II rickets model rats using vitamin D receptor-expressing adenovirus vector
- Vitamin D dependent rickets type 2: a case-based review of patient with alopecia and rickets
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness
- Androgenic alopecia and its association with metabolic syndrome
- A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21.
- Keratosis pilaris atrophicans faciei: An observational, descriptive, retrospective clinical study
- Androgenetic Alopecia
- Self-Amplifying RNA Approach for Protein Replacement Therapy
- Clinical, histopathological and immunological characteristics of exfoliative cutaneous lupus erythematosus in 25 German short‐haired pointers
- BH26 First reported case of lichen planopilaris in siblings: evidence for a genetic link?
- Alopecia areata: recognition, diagnosis and management
- P138 Hormonal parameters in androgenetic alopecia of the male
- Noninflammatory, Nonpruritic Alopecia of Horses
- A Technique for Reconstruction of Eyebrows and Eyelashes
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Ulerythema ophryogenes (keratosis pilaris atrophicans faciei).
- Sebaceous Adenitis in an Akita: Symptoms and Therapeutic Approaches
- Male Androgenetic Alopecia — Endotext
- Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia
- Monilethrix: a typical case report with microscopic and dermatoscopic findings
- Familial Frontal Fibrosing Alopecia
- Kératose pilaire
- Loose Anagen Hair as a Cause of Hereditary Hair Loss in Children
- HAIR AND SYSTEMATIC DISEASE
- Hair Loss in Systemic Disease
- Diseases of Periocular Hair
- Hair in health and disease: an introduction
- Computational derivation of a molecular framework for hair follicle biology from disease genes
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex