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Research 271–300 of 784
- Acetyl-CoA synthesis in the skin is a key determinant of systemic lipid homeostasis
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms
- Skin Appendage Proteins of Tetrapods: Building Blocks of Claws, Feathers, Hair and Other Cornified Epithelial Structures
- Contents
- The genetics of alopecia areata: New approaches, new findings, new treatments
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Ichthyosis Follicularis With Alopecia and Photophobia
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Genetics of Inherited Ichthyoses and Related Diseases
- Care of the newborn with ichthyosis
- Inherited ichthyosis: Syndromic forms
- Neonatal Ichthyosis and Sclerosing Cholangitis Syndrome
- Ichthyosis follicularis, alopecia and photophobia (IFAP) syndrome treated with acitretin
- Ichthyosis with confetti: clinics, molecular genetics and management
- Ichthyosis follicularis with alopecia and photophobia in a mother and daughter
- A novel mutation in the connexin 26 gene (<i>GJB2</i>) in a child with clinical and histological features of keratitis–ichthyosis–deafness (KID) syndrome
- Severe form of keratitis–ichthyosis–deafness (KID) syndrome associated with septic complications
- Nutritional Status and Gastrointestinal Structure and Function in Children With Ichthyosis and Growth Failure
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- New developments in the molecular treatment of ichthyosis: review of the literature
- Molecular Genetics of Keratinization Disorders – What’s New About Ichthyosis
- Follicular ichthyosis
- Netherton's syndrome and ichthyosis linearis circumflexa.
- A Japanese case of ichthyosis follicularis with atrichia and photophobia syndrome with an MBTPS2 mutation
- Clearance of ichthyosis linearis circumflexa with balneophototherapy
- Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome
- Recent advances in congenital ichthyoses
- Ichthyosis linearis circumflexa in a child. Response to narrowband UVB therapy.