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Research 151–180 of 483
- Nutritional Disorders of the Hair and Their Management
- Beard Alopecia: An Updated and Comprehensive Review of Etiologies, Presentation and Treatment
- Erosive Pustular Dermatosis: Delving into Etiopathogenesis and Management
- <i>In vivo</i> response of GsdmA3<sup>Dfl</sup>/+ mice to topically applied fish oil – effects on cellular markers and macrophages
- Poster Presentations at the 28th Joint Meeting of the International Society of Dermatopathology, March 5–6, 2025, Orlando, Florida, USA
- Cutaneous Adverse Drug Reactions to Antibiotics: How Much is the Extent of the Problem?
- Rare Cutaneous Side Effects of Imiquimod: A Review on Its Mechanisms, Diagnosis, and Management
- Ernährungsstörungen des Haares und deren Management
- 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
- 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
- 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
- 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].
- A review of acitretin, a systemic retinoid for the treatment of psoriasis
- Oral Treatment of Keratinizing Disorders of Skin and Mucous Membranes With Etretinate
- Trichoscopy as a diagnostic tool in trichorrhexis invaginata and Netherton syndrome
- Follicular mucinosis in association with Sezary syndrome
- Alopecia Universalis Associated with Cutaneous T Cell Lymphoma
- Generalized pustular psoriasis responsive to PUVA and oral cyclosporin therapy
- Immunomodulators in the treatment of cutaneous lymphoma
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Missense mutation Y449H of the K10 gene in a patient with severe epidermolytic ichthyosis
- Psoriasis and Related Disorders
- Acitretin for the Treatment of Psoriasis: A Case Report of Long-Lasting Alopecia
- An unusual case of increased hair pigmentation in previously grey-white hair