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Research 91–120 of 483
- Subacute cutaneous lupus erythematosus presenting as erythroderma
- Dapsone-induced erythroderma with Beau's lines
- 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
- 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
- Generalized pustular psoriasis responsive to PUVA and oral cyclosporin therapy
- Psychoactive drugs and skin
- 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
- Omenn syndrome in a 10-month-old male with athymia and VACTERL association
- 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
- Severe pityriasis rubra pilaris complicated with Kaposi's varicelliform eruption and cutaneous MRSA infection case report
- [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
- Skin Manifestations in Primary Immunodeficient Children
- Stanozolol in the Treatment of Pityriasis Rubra Pilaris
- Characterizing Disease Features and Other Medical Diagnoses in Patients With Pityriasis Rubra Pilaris