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Research 961–990 of 1000+
- A General Paediatric Approach to Ankyloblepharon–Ectodermal Dysplasia–Cleft Lip/Palate Syndrome in Infancy: A Case Report
- Cutaneous Manifestations in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED): A Comprehensive Review
- A novel EDA variant that causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family
- Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome with Concomitant Lymphopenia: A Novel TP63 Mutation
- Trichothiodystrophy: Review of sulfur-deficient brittle hair syndromes and association with the ectodermal dysplasias
- Breakdown of Immune Tolerance in AIRE-Deficient Rats Induces a Severe Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy–like Autoimmune Disease
- 1435 Dynamic morphogen-p63 chromatin interactions that guide epigenetic changes and p63 activity in surface ectoderm commitment
- A Unique Case of Trichorrhexis Nodosa—"Bamboo Hairs"
- Altered skin development and impaired proliferative and inflammatory responses in transgenic mice overexpressing the glucocorticoid receptor
- Myodegeneration in EDA-A2 Transgenic Mice Is Prevented by XEDAR Deficiency
- Familial Uncombable Hair Syndrome: Ultrastructural Hair Study and Response to Biotin
- Trichoscopy in Hair Shaft Disorders
- Ichthyosis with confetti: clinics, molecular genetics and management
- Atrichia With Papular Lesions
- Ectodysplasin research—Where to next?
- Gastrointestinal polyposis with protein-losing enteropathy, abnormal skin pigmentation and loss of hair and nails (Cronkhite-Canada syndrome)
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Inherited disorders of the skin in human and mouse: from development to differentiation.
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Ulerythema Ophryogenes
- Genetics of Structural Hair Disorders
- Hair shaft disorders in children – An update
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- A Scandinavian case of skin fragility, alopecia and cardiomyopathy caused by<i>DSP</i>mutations
- Congenital atrichia and hypotrichosis
- Clinical Case Notes. Propecia-associated bilateral cataract
- Hair loss among a group of Egyptian children
- Canestick Lesion of Vellus Hair in Netherton's Syndrome
- Transcriptional activation of a subset of hair keratin genes by the NF-κB effector p65/RelA
- Whiskers amiss, a new vibrissae and hair mutation near the Krt1 cluster on mouse Chromosome 11