Search
for
Sort by
Research 30 of 1000+
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- PA33 When bones speak through nails: insights from a paediatric case series
- Hair and Nail Relationship
- Comparative Anatomy of Mouse and Human Nail Units
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- Child with De Novo t(1;6)(p22.1;p22.1) translocation and features of ectodermal dysplasia with hypodontia and developmental delay
- The skin manifestations in end-stage renal disease patients in Jordan, single-center experience
- PA05 A rare case of cardiocutaneous syndrome in a young child
- A 9-month-old infant with severe scalp dermatosis
- Two‐Year Follow‐Up of Ectodermal Dysplasia‐Syndactyly Syndrome 1 in a Palestinian Child Successfully Treated With Topical Minoxidil and Tretinoin: A Case Report
- Top applications of dermatologic ultrasonography that can modify management
- Pigmentary mosaicism: An update
- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Normal Ultrasound Anatomy of the Skin, Nail, and Hair
- Hair and nail involvement in lupus erythematosus
- Prevalence Study of Dermatologic Manifestations among Diabetic Patients
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Kartagener Syndrome With Ectodermal Anomalies in An Adolescent Female: A Case Report
- Hair Anomalies in a 6-Year-Old Girl
- Immunology of the Human Nail Apparatus: The Nail Matrix Is a Site of Relative Immune Privilege
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Comparison of cutaneous manifestations in chronic kidney disease with or without dialysis
- Involvement of scalp and nails in lupus erythematosus
- Semiology of skin toxicity associated with epidermal growth factor receptor (EGFR) inhibitors
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- The Skin and Subcutaneous Tissues
- Uncombable hair syndrome and beyond