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Research 91–120 of 1000+
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- Keratin 17 null mice exhibit age- and strain-dependent alopecia
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Congenital hypotrichosis due to short anagen
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Cutaneous features of myotonic dystrophy types 1 and 2: Implication of premature aging and vitamin D homeostasis
- Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Encephalocraniocutaneous lipomatosis: congenital alopecia treatment in a rare neurocutaneous syndrome
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- Forme létale de syndrome de Netherton au sein d’une famille multiplex consanguine
- Ptosis in childhood
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- [Trichothiodystrophy: a morphological and biochemical study].
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Clouston’s syndrome: a rare case report
- Altered skin development and impaired proliferative and inflammatory responses in transgenic mice overexpressing the glucocorticoid receptor
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- Bachmann–Bupp syndrome and treatment
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Keratins and disease at a glance
- Hedgehog Signaling, Keratin 6 Induction, and Sebaceous Gland Morphogenesis
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- BH15 Nonsyndromic hypotrichosis: a rare case of congenital hypotrichosis 15 and management with minoxidil
- Unruly hair
- Hair loss
- Hair loss and its management in children