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Research 541–570 of 1000+
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- [Dermatophytic disease: exuberant hyperkeratosis with cutaneous horns].
- [Hormonal profile in men with premature androgenic alopecia].
- POLY CYSTIC OVARIAN SYNDROME: AN UPDATED REVIEW
- Inheritance-Specific Dysregulation of Th1- and Th17-Associated Cytokines in Alopecia Areata
- Co-occurrence of monilethrix and Type 1 diabetes mellitus
- Nevoid basal carcinoma syndrome (Gorlin syndrome) and pronounced androgenic alopecia in a woman with a novel mutation p.Leu1159fsx32 in the PTCH gene
- Clinical case of alopecia totalis in pediatric practice
- CCDC22 and CCDC93, two potential retriever-interacting proteins, are required for root and root hair growth in Arabidopsis
- Polikistik Over Sendromu ve Obezite: FTO ve MC4R Gen Polimorfizmlerinin Rolü
- 268 Male-pattern baldness and its association with coronary heart disease
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Woolly Antics between the Sheaths
- Hair follicle stem cell replication stress drives IFI16/STING-dependent inflammation in hidradenitis suppurativa
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Precocious puberty: the unlikely herald of Familial adenomatous polyposis in a young girl
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- Multiple basal cell carcinomas in a patient with myotonic dystrophy type 1
- Fertility and Sterility Vol 101 No 4, April 2014
- British Society for Dermatopathology
- Comparative Skin Transcriptomics Reveals Key Regulators of Cashmere Fiber Production in Inner Mongolian Goats
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Correlation between Pilomatrixoma and Polycystic Ovary Syndrome (PCOS)
- Localized variant of junctional epidermolysis bullosa with R795X mutation
- Analysis of the Long Non-Coding and Messenger RNA Expression Profiles in the Skin Tissue of Super Merino and Small-Tailed Han Sheep
- Pearly Pinna Papules in a Young Female
- Research Snippets
- An Autosomal Recessive Woolly Hair/Hypotrichosis Case with LIPH Mutation in a Turkish Patient
- A Complex Clinical Situation in Polycystic Ovary Syndrome: HAIR‐AN Syndrome ‘‘Case Report’’