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Research 31–60 of 1000+
- Current Genetics in Hair Diseases
- Polarized microscopy in genetic hair disorders: case series
- N02. Hair and Nails
- Familial Uncombable Hair Syndrome: Ultrastructural Hair Study and Response to Biotin
- Hypotrichosis and nail dysplasia: A novel hidrotic ectodermal dysplasia
- Child with De Novo t(1;6)(p22.1;p22.1) translocation and features of ectodermal dysplasia with hypodontia and developmental delay
- Topical cetirizine and oral vitamin D: a valid treatment for hypotrichosis caused by ectodermal dysplasia
- [Sodium valproate-induced kinky hair].
- Molecular Basis of Hereditary Hair Diseases
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- Alopecia areata in a patient with WNT10A heterozygous ectodermal dysplasia
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- High‐Potency Topical Steroids: An Effective Therapy for Chronic Scalp Inflammation in Rapp–Hodgkin Ectodermal Dysplasia
- Hair Loss in Children, Etiologies, and Treatment
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- Identification of Ectodysplasin Target Genes Reveals the Involvement of Chemokines in Hair Development
- Genetic hair and nail disorders
- Ectodermal Dysplasia: Otolaryngologic Manifestations and Management
- Anhidrotic Ectodermal Dysplasia: Predisposition to Bronchial Disease
- Follicular dysplasia in five Weimaraners
- Epidermal dysplasia and <i>Malassezia</i> infection in two West Highland White Terrier siblings: an inherited skin disorder or reaction to severe <i>Malassezia</i> infection?
- Suppression of hair follicle development inhibits induction of sonic hedgehog, patched, and patched-2 in hair germs in mice
- A four generation hidrotic ectodermal dysplasia family: an allelic variant of Clouston syndrome?
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Short anagen hair syndrome is caused by mutations in the <i>WNT10A</i> gene and has a genetic overlap with male pattern hair loss
- 092 Novel biallelic RIPK4 mutations cause ectodermal dysplasia with cutaneous syndactyly
- Genetic characterization of congenital defects in dogs : caudal dysplasia, ectodermal dysplasia and mucopolysaccharidosis VII