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Research 91–120 of 1000+
- Epidermolysis bullosa in animals: a review
- Androgenic alopecia and its association with metabolic syndrome
- Escobar syndrome (multiple pterygium syndrome) associated with osteogenesis imperfecta: a case report
- Cronkhite-Canada syndrome: An elusive gastrointestinal disorder with multisystem involvement-pathogenesis, diagnosis, and therapeutic strategies
- A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21.
- LibGuides: L3Y2 Tutorial 2022 - critical thinking: Claim 5: Caffeine reduces hair loss
- Androgenetic Alopecia
- Self-Amplifying RNA Approach for Protein Replacement Therapy
- Hair Shaft Dysplasias
- Keratosis pilaris atrophicans faciei: An observational, descriptive, retrospective clinical study
- Clinical, histopathological and immunological characteristics of exfoliative cutaneous lupus erythematosus in 25 German short‐haired pointers
- Familial Frontal Fibrosing Alopecia
- Hidradenitis Suppurativa/Acne Inversa/Dissecting Terminal Hair Folliculitis
- Hair and nail disorders of childhood
- Kératose pilaire
- Ulerythema ophryogenes (keratosis pilaris atrophicans faciei).
- 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
- Hair loss
- Alopecia areata: recognition, diagnosis and management
- The Interplay between Finasteride-Induced Androgen Imbalance, Endoplasmic Reticulum Stress, Oxidative Stress, and Liver Disorders in Paternal and Filial Generation
- Noninflammatory, Nonpruritic Alopecia of Horses
- Sebaceous Adenitis in an Akita: Symptoms and Therapeutic Approaches
- Male Androgenetic Alopecia — Endotext
- A Technique for Reconstruction of Eyebrows and Eyelashes
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- Loose Anagen Hair as a Cause of Hereditary Hair Loss in Children
- Gender aspects in skin diseases
- Anaemia and skin disease
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2