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Research 181–210 of 227
- Tricotiodistrofia. Reporte de un caso
- Ichthyosis
- Collodion baby case series: the success of oral retinoic acid
- Chronic Ulceration of the Scalp Associated with Genetically Different Types of Congenital Ichthyosis: A Series of Four Cases
- Early Skin Biopsy in Conradi‐Hünermann‐Happle Syndrome (X‐Linked Dominant Chondrodysplasia Punctata)
- 152 Alopecia patterns in patients with autosomal receesive congenital ichthyosis
- Genes of Congenital Dermatologic Disorders in Dogs—A Review
- Trichothiodystrophy in a child with occult learning disorder
- Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Disorders of Keratinization
- Low-sulfur hair syndrome associated with UVB photosensitivity and testicular failure
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- AN UPDATE OF HAIR SHAFT DISORDERS
- High-sulfur protein deficient human hair: clinical aspects and biochemical study of two unreported cases of a variant type of trichothiodystrophy
- Graham‐Little Piccardi Lassueur syndrome and review of the literature
- Erythroderma: clinical and etiological study of 88 cases seen in a tertiary hospital over 25 years
- “Peeling paint” dermatosis in a leukemia patient
- Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis
- Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs
- Keratitis-Ichthyosis-Deafness Syndrome Caused by Missense Mutation in GJB2 Encoding Connexin 26 in a Chinese Patient
- Graham-Little Piccardi Lassueur Syndrome and review of the literature
- Trichorrhexis Invaginata and Netherton’s Syndrome
- The ultrastructure of the interfollicular epidermis of the hairless (hr/hr) mouse
- Spink5-deficient mice mimic Netherton syndrome through degradation of desmoglein 1 by epidermal protease hyperactivity
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- Proteome Analysis of Human Hair Shaft
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Changing Patterns of Localization of Putative Stem Cells in Developing Human Hair Follicles
- Peptidylarginine Deiminase Isoforms Are Differentially Expressed in the Anagen Hair Follicles and Other Human Skin Appendages