Search
for
Sort by
Research 151–180 of 172
- Dissecting Cellulitis of the Scalp: Linking Pathogenesis to Therapy
- When Rare Meets Risky: Clouston Syndrome with Cutaneous Squamous Cell Carcinoma
- Dermatology Patient Support Groups
- Cornified Epithelial Teeth of Jawless Vertebrates Contain Proteins Similar to Keratin-Associated Proteins of Mammalian Skin Appendages
- Clinicopathologic Case 2: Multiple Intraoral White Lesions in a 55-year-old Female
- Bioengineered skin organoids: from development to applications
- The Non-Cosmetic Dermatological Use of Botulinum Neurotoxin
- Generalized multiple eruptive milia in an infant – An unusual presentation
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- Deep Hair Phenomics: Implications in Endocrinology, Development, and Aging
- Hair-Thread Tourniquet Syndrome; Emergent Diagnosable Condition
- Protein profiling of forehead epidermal corneocytes distinguishes frontal fibrosing from androgenetic alopecia
- Proceedings of the Inaugural Pediatric Dermatology Research Alliance (PeDRA) Conference
- Acquired Localized Longitudinal Pachyonychia and Onychomatrical Tumors: A Comparative Study to Onychomatricomas (5 Cases) and Onychocytic Matricomas (4 Cases)
- PA05 A rare case of cardiocutaneous syndrome in a young child
- Interventions for nail psoriasis
- Optimal Management of Plaque Psoriasis in Adolescents: Current Perspectives
- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14
- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- Enteropathica Acrodermatitis Complicated by Necrotising Fasciitis in an Infant Admitted to the Paediatric Emergency Department of the Gabriel Touré University Hospital
- Case report: Acrodermatitis enteropathica result from a novel SLC39A4 gene mutation
- Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21.
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Pachyonychia Congenita-Associated Alopecia. A Microscopic Analysis Using Transverse Section Technique
- A new type of pachyonychia congenita.
- Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b
- KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies