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Research 121–150 of 1000+
- Cutaneous Manifestations of Mucopolysaccharidoses
- Keratosis Follicularis Spinulosa Decalvans. What Syndrome Is This?
- Lipedematous scalp with lipedematous alopecia: A case report
- Psoriasis and Related Disorders
- LAMELLAR ICHTHYOSIS: ONE CASE REPORT
- VITILIGO: WHAT’S OLD, WHAT’S NEW?
- Skin Pigmentation Types, Causes and Treatment—A Review
- Nociceptive and Nonnociceptive Roles of TRPV3 and Its “Druggability”
- Alopecia Areata
- Alopecia areata - probing the deforestation
- Case of non-Herlitz junctional epidermolysis bullosa with<i>COL17A1</i>mutation
- Regional Dermatology
- Multiple facial atrophic scars in childhood
- Lymphoproliferative Disorders: Hot Topics in Dermatology 2019
- Proceedings of the Inaugural Pediatric Dermatology Research Alliance (PeDRA) Conference
- Geriatric Dermatology: Overview
- Australian Hair and Wool Research Society Cutaneous Biology and Endocrinology Workshop
- The Rotterdam Study: 2016 objectives and design update
- Polycystic Ovary Syndrome (PCOS): From Diagnosis to Treatment
- Vogt-Koyanagi-Harada Disease with Oral Manifestations: A Rare Case Report
- Hypotrichosis in a child with olmsted syndrome
- Hidradenitis Suppurativa: From Physiopathologies to Targeted Therapeutics
- Hidradenitis Suppurativa: From Physiopathologies to Targeted Therapeutics
- Clinical Snippets
- Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b
- Melasma and Endocrine Disorders
- Disorders of Hair Pigmentation
- Supplementary Material for: Case report - Hair shaft normalization and hair growth in SPINK5-syndromic epidermal differentiation disorder (Netherton syndrome) while on treatment with dupilumab: a novel therapeutic approach for Trichorrhexis invaginata
- Supplementary Material for: Case report - Hair shaft normalization and hair growth in SPINK5-syndromic epidermal differentiation disorder (Netherton syndrome) while on treatment with dupilumab: a novel therapeutic approach for Trichorrhexis invaginata
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction