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Research 691–720 of 1000+
- Th,-e mechanistic insights into the application of retinoids and possible adjunct therapeutic treatment to androgenic alopecia
- A review of isotretinoin in the treatment of frontal fibrosing alopecia
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Monilethrix: a typical case report with microscopic and dermatoscopic findings
- Pulmonary manifestations of Birt-Hogg-Dubé syndrome
- P-18 THREE BODY PROBLEM PATIENT: EHLER DANLOS SYNDROME COMBINED WITH HYPOPHOSPHATASIA AND FATTY ACID OXIDATION DEFECT
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Ectodermal Dysplasia: Variable Expressions
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- Hormonal regulation in male androgenetic alopecia—Sex hormones and beyond: Evidence from recent genetic studies
- Substance P in keratosis follicularis spinulosa decalvans
- Advances in the genetic understanding of hypohidrotic ectodermal dysplasia
- Exploring the Dermoscopic Patterns in Tuberous Sclerosis
- Ehlers-Danlos syndrome: From bedside to bench
- Genetics and Epigenetics of Polycystic Ovary Syndrome
- Central centrifugal cicatricial alopecia: challenges and solutions
- Fibrodysplasia Ossificans Progressiva (FOP): A Segmental Progeroid Syndrome
- Ichthyosis
- Ichthyosis with confetti: clinics, molecular genetics and management
- Effectiveness of Rosmarinus officinalis for Androgenetic Alopecia: A Literature Review
- Keratosis Follicularis Squamosa in Unilateral Buttock: A Case Report and Review of Literature in China
- Assessment of the usefulness of dihydrotestosterone in the diagnostics of patients with androgenetic alopecia
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Acne Vulgaris
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Pathology of Mouse Models of Accelerated Aging
- New developments in the molecular treatment of ichthyosis: review of the literature