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Research 121–150 of 230
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Ingestion of a dietary supplement resulting in selenium toxicity
- Genetic Hair Disorders: A Review
- Poster Presentations
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- New developments in the molecular treatment of ichthyosis: review of the literature
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Off-label uses of retinoids in dermatology
- Medical Dermatology
- Phenotyping mice with skin, hair, or nail abnormalities: A systematic approach and methodologies from simple to complex
- Case Report of Wound Treatment with Hyiodine Gel in an Occasional KID Syndrome Patient
- Poster Presentations at the 28th Joint Meeting of the International Society of Dermatopathology, March 5–6, 2025, Orlando, Florida, USA
- Uncommon Presentation of Pityriasis Rubra Pilaris of the Scalp: Clinical, Trichoscopic, and Histopathologic Features and Review of the Literature
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- A syndrome of congenital ichthyosis, mental retardation, myopathy and anemia in dizygotic twin sisters
- Ichthyosiform Rash and Fever in a Child
- Extensive Ichthyosiform Sarcoidosis in a Patient With Juvenile Rheumatoid Arthritis
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- Case of epidermolytic ichthyosis (bullous congenial ichthyosiform erythroderma) with a novel L157P mutation in KRT10 complicated by hypercalcemia
- [Black piedra in South Africa. 1st description in a child with bamboo hair, pili torti and congenital erythroderma ichthyosiforme].
- Care of the newborn with ichthyosis
- Ichthyosis with confetti: clinics, molecular genetics and management
- 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
- Forme létale de syndrome de Netherton au sein d’une famille multiplex consanguine
- [The Netherton syndrome with alopecia and prolinuria].
- Improvement of Skin Lesions in an Adult with CHILD Syndrome Treated with 2% Ketoconazole Cream
- Bamboo Hair Syndrome or Netherton Syndrome - A Case Report
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation