Search
for
Sort by
Research 30 of 1000+
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- 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
- KERATINS AND SKIN DISORDERS
- The keratins and their disorders
- Ichthyosis with confetti: a rare diagnosis and treatment plan
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- Trichoscopy in Unveiling the Triad of Netherton Syndrome
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Ichthyosis with confetti: clinics, molecular genetics and management
- Early skin biopsy is helpful for the diagnosis and management of neonatal and infantile erythrodermas
- Erythroderma: clinical and etiological study of 88 cases seen in a tertiary hospital over 25 years
- Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis.
- Ichthyosis
- JAK-Inhibitors Beyond the Label: Emerging Applications in Dermatology
- Trichoscopy as a diagnostic tool in trichorrhexis invaginata and Netherton syndrome
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Dupilumab in Inflammatory Skin Diseases: A Systematic Review
- Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings
- Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders
- Folliculotropic mycosis fungoides in a child: a rare case
- Cushing Syndrome from Percutaneous Absorption of 1% Hydrocortisone Ointment in Netherton Syndrome
- Oral Retinoids in Dermatology
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Pattern of Skin disorders across age groups
- The human keratins: biology and pathology
- Keratin disorders: from gene to therapy
- Beyond Expectations
- Chemotherapy of psoriasis and other skin disorders with oral retinoids
- Fatty acids and related lipid mediators in the regulation of cutaneous inflammation