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Research 61–90 of 1000+
- Congenital atrichia and hypotrichosis
- Hypotrichosis with juvenile macular dystrophy
- Cronkhite-Canada syndrome: A rare disease presenting with dermatological and gastrointestinal manifestations
- Alymphoid cystic thymic dysgenesis - FOXN1 gene mutation: a rare case report of two siblings
- Case of Cronkhite Canada Syndrome - A Non-Inherited Gastrointestinal Polyposis Syndrome
- N02. Hair and Nails
- Mechanical forces in skin disorders
- Human Induced Pluripotent Stem Cell–Derived Ectodermal Precursor Cells Contribute to Hair Follicle Morphogenesis In Vivo
- Hair loss among a group of Egyptian children
- Polarized microscopy in genetic hair disorders: case series
- Inherited Disorders of the Hair
- Biology and Genetics of Hair
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- When the algorithm fails and experience wins: An extraordinary trichoscopic case
- Inherited Epidermolysis Bullosa: A Clinical Case
- Pathogenesis and clinical features of alopecia in epidermolysis bullosa: A systematic review
- Existence of Neural Crest–Derived Progenitor Cells in Normal and Fuchs Endothelial Dystrophy Corneal Endothelium
- A Forty-Two-Year-Old Male with Multiple Gastrointestinal Polyps, Cutaneous Manifestations, and Nail Dystrophy
- Keratin expression by corneal and limbal stem cells during development
- A Case Report of Cronkhite-Canada Syndrome Complicated by Membranous Nephropathy
- Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- Genetic Hair Disorders: A Review
- PA33 When bones speak through nails: insights from a paediatric case series
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- Recombinant Thrombomodulin Used to Successfully Treat Cronkhite-Canada Syndrome with Disseminated Intravascular Coagulation due to Sepsis in a Compromised Patient
- When Rare Meets Risky: Clouston Syndrome with Cutaneous Squamous Cell Carcinoma
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation