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Research 91–120 of 227
- Vitamins
- Collodion baby case series: the success of oral retinoic acid
- Off-label dermatologic uses of IL-23 inhibitors
- Early Skin Biopsy in Conradi‐Hünermann‐Happle Syndrome (X‐Linked Dominant Chondrodysplasia Punctata)
- 152 Alopecia patterns in patients with autosomal receesive congenital ichthyosis
- Novel association of trichothiodystrophy with autoimmune thyroiditis and autoimmune hemolytic anemia: A case report
- Trichothiodystrophy in a child with occult learning disorder
- Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities
- Pigmentary Puzzle: A Rare Case of Hyperpigmented Cutaneous Sarcoidosis
- Netherton syndrome subtypes share IL-17/IL-36 signature with distinct IFN-α and allergic responses
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Disorders of Keratinization
- Low-sulfur hair syndrome associated with UVB photosensitivity and testicular failure
- Poster Presentations
- 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
- <i>NIPAL4</i> deletion identified in an American Bully with autosomal recessive congenital ichthyosis and response to topical therapy
- Ichthyosis hystrix
- Rickets in association with skin diseases and conditions: A review with emphasis on screening and prevention
- Positive Impact of Fish Oil on Diabetic and Hypercholestrolemic Skin Disorders
- LEKTI: Netherton Syndrome and Atopic Dermatitis
- 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
- “Degeneration” in Dermatopathology
- Keratitis-Ichthyosis-Deafness Syndrome Caused by Missense Mutation in GJB2 Encoding Connexin 26 in a Chinese Patient
- Trichorrhexis Invaginata and Netherton’s Syndrome
- Spink5-deficient mice mimic Netherton syndrome through degradation of desmoglein 1 by epidermal protease hyperactivity
- Kaposi varicelliform eruption
- The ultrastructure of the interfollicular epidermis of the hairless (hr/hr) mouse
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing