Search
for
Sort by
Research 61–90 of 1000+
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Morpho-Regulation of Ectodermal Organs
- 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>
- Alopecia areata: Clinical presentation, diagnosis, and unusual cases
- Epidermal Dysplasia and Abnormal Hair Follicles in Transgenic Mice Overexpressing Homeobox Gene MSX-2
- Micronutrients for Hair and Nails
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- 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
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Evaluation of Clinical and Oral Findings in Patients with Epidermolysis bullosa
- Analogs of human genetic skin disease in domesticated animals
- ALOPECIA AREATA-A CLINICAL ANALYSIS
- Disorders of the skin appendages
- A clinico-epidemiological study of scalp hair loss in children (0–18 years) in Kota Region, South-East Rajasthan