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Research 91–120 of 1000+
- Collodion baby to bathing suit ichthyosis: A 6-year follow-up
- Netherton syndrome: effect on ichthyosis linearis circumflexa with dupilumab
- Updated strategies for the management, pathogenesis and molecular genetics of different forms of ichthyosis syndromes with prominent hair abnormalities
- Lamellar ichthyosis, dwarfism, mental retardation, and hair shaft abnormalities
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- First Symposium of Ichthyosis Experts
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Hair loss and its management in children
- Hair Shaft Dysplasias
- Diseases of Periocular Hair
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Immunological control of skin development: from homeostasis to developmental pathologies
- Dermatoscopy of hair shaft disorders
- Madarosis, milphosis, eyelash trichomegaly, and dermatochalasis
- Trichothiodystrophy without associated neuroectodermal features in two siblings
- Collodion baby case series: the success of oral retinoic acid
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production
- Disorders of Keratinization
- Netherton Syndrome – Responding to Oral Retinoids
- AN UPDATE OF HAIR SHAFT DISORDERS
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Keratin gene mutations in disorders of human skin and its appendages
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Efficient In Vitro Transfection of Human Keratinocytes with an Adenovirus-Enhanced Receptor-Mediated System
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice