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Research 511–540 of 517
- Genetics
- A syndrome of congenital ichthyosis, mental retardation, myopathy and anemia in dizygotic twin sisters
- Subject Index
- DIETHYLPROPION
- Update in Dermatology
- Recessive Epidermolysis Bullosa Simplex Phenotype Reproduced in Vitro
- Implication of Human Bacterial Gut Microbiota on Immune-Mediated and Autoimmune Dermatological Diseases and Their Comorbidities: A Narrative Review
- Subacute cutaneous lupus erythematosus presenting as erythroderma
- Dapsone-induced erythroderma with Beau's lines
- Erythroderma: clinical and etiological study of 88 cases seen in a tertiary hospital over 25 years
- Erythroderma, Alopecia, Anhidrosis, and Vitiligo as Complications of a Red Ink Tattoo—A Case Report
- Erythrodermic Psoriasis in the Context of Emerging Triggers: Insights into Dupilumab-Associated and COVID-19-Induced Psoriatic Disease
- Ixekizumab Improved Refractory Erythrodermic Psoriasis with Comorbid Diffuse Alopecia: A Case Report with 52-Week Follow-Up
- Clinico-etiological and histopathological correlation in erythroderma: In a tertiary care hospital of Eastern Odisha
- Ichthyosiform Erythroderma, a Multifaceted Syndromic Entity
- Case of epidermolytic ichthyosis (bullous congenial ichthyosiform erythroderma) with a novel L157P mutation in KRT10 complicated by hypercalcemia
- Early skin biopsy is helpful for the diagnosis and management of neonatal and infantile erythrodermas
- Érythrodermies néonatales et infantiles : apport de la biopsie cutanée précoce dans les formes graves
- Excessive hair growth in a patient with psoriatic erythroderma following secukinumab administration
- 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
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- 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
- [Black piedra in South Africa. 1st description in a child with bamboo hair, pili torti and congenital erythroderma ichthyosiforme].
- [Netherton's syndrome in two sisters].
- Graft versus host disease–like: A new paraneoplastic syndrome
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- A review of acitretin, a systemic retinoid for the treatment of psoriasis
- Skin Manifestations in Primary Immunodeficient Children
- Oral Treatment of Keratinizing Disorders of Skin and Mucous Membranes With Etretinate
- Trichoscopy as a diagnostic tool in trichorrhexis invaginata and Netherton syndrome