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Research 61–90 of 1000+
- 190 A cross-sectional study evaluating skin, hair, nail and bone disease in patients with focal dermal hypoplasia
- Ectodermal Dysplasia: Variable Expressions
- Biotin
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Epidermal Dysplasia and Abnormal Hair Follicles in Transgenic Mice Overexpressing Homeobox Gene MSX-2
- Dermatopathology and molecular genetics
- Wnt Signaling Across Adult Skin Mini-Organs: Interfollicular Epidermis, Hair Follicle, and Nail—Implications for Disease and Regeneration
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- A Review of the Use of Biotin for Hair Loss
- Hair shaft disorders in children – An update
- Westwood Carolina Conference on Clinical Dermatology
- A Forty-Two-Year-Old Male with Multiple Gastrointestinal Polyps, Cutaneous Manifestations, and Nail Dystrophy
- Keratinocyte-specific ablation of the NF-κB regulatory protein A20 (TNFAIP3) reveals a role in the control of epidermal homeostasis
- Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- A Case Report of Cronkhite-Canada Syndrome Complicated by Membranous Nephropathy
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- Autoimmune polyendocrine syndrome type 1 a case report from Bangladesh
- Cronkhite-Canada Syndrome Associated with Serrated Adenoma and Malignant Polyp: A Case Report and a Literature Review of 13 Cronkhite-Canada Syndrome Cases in Korea
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Evaluation of Clinical and Oral Findings in Patients with Epidermolysis bullosa
- Micronutrients for Hair and Nails
- Analogs of human genetic skin disease in domesticated animals
- ALOPECIA AREATA-A CLINICAL ANALYSIS
- A clinico-epidemiological study of scalp hair loss in children (0–18 years) in Kota Region, South-East Rajasthan
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- Congenital atrichia associated with situs inversus and mesocardia
- Pathophysiology of Alopecia Areata in the Pediatric Patient
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins