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Research 361–390 of 387
- 481 Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis
- A linear and reticulate crusted keratotic papulopustular eruption: a rare presentation of PRIDE (Papulopustules and/or paronychia, Regulatory abnormalities of hair growth, Itching, and Dryness due to Epidermal growth factor receptor inhibitors) complex
- Severe pityriasis rubra pilaris complicated with Kaposi's varicelliform eruption and cutaneous MRSA infection case report
- Clinicopathologic Case 2: Multiple Intraoral White Lesions in a 55-year-old Female
- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14
- Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs
- Rare Cutaneous Side Effects of Imiquimod: A Review on Its Mechanisms, Diagnosis, and Management
- Alopecias: Practical Tips for the Management of Biopsies and Main Diagnostic Clues for General Pathologists and Dermatopathologists
- Dermatoses in Postmenopausal Women in a Tertiary Health Care Center of Bihar: A Prospective Cross-Sectional Study
- Study on Autoimmune Thyroid Disorders in Chronic Spontaneous Urticaria at a Tertiary Care Central Rural Hospital in India
- Dermatologic manifestations of thyroid disease: a literature review
- Genome-wide detection of RNA editing events during the hair follicles cycle of Tianzhu white yak
- Recurrent pruritic polymorphic lesions associated with weight loss
- The Non-Cosmetic Dermatological Use of Botulinum Neurotoxin
- [Translated article] Keys to the Diagnosis of Hair Shaft Disorders: Part II
- Circle Hairs in a Patient with Multiple Myeloma
- Clouston’s syndrome: a rare case report
- Proceedings of the Ninth World Congress for Hair Research (2015)
- Skin, Genetic Defects, and Aging
- Viva questions from the IJDVL
- Subject Index
- TONGUE, RED
- Skin Manifestations of Rheumatological Diseases
- Protein profiling of forehead epidermal corneocytes distinguishes frontal fibrosing from androgenetic alopecia
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- SUN-585 A Case of Atypical Myxedema in Hypothyroidism
- Structural and biochemical changes underlying a keratoderma-like phenotype in mice lacking suprabasal AP1 transcription factor function
- Spiny keratoderma ‐ a demonstration of hair keratin and hair type keratinization
- Recessive Mutation in FAM83G Associated with Palmoplantar Keratoderma and Exuberant Scalp Hair