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Research 301–330 of 509
- Clinicopathologic features, demographics, disease burden, and therapeutics in alopecic sarcoidosis: a case series and systematic review
- The Spectrum of Cutaneous Manifestations in Lupus Erythematosus: A Comprehensive Review
- SKIN MANIFESTATIONS OF RHEUMATOLOGICAL DISEASES
- Micropigmentation
- Seborrheic dermatitis and pityriasis sicca: A review
- DIETHYLPROPION
- Genetic Hair Disorders: A Review
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines
- 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
- Érythrodermies néonatales et infantiles : apport de la biopsie cutanée précoce dans les formes graves
- 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
- [Black piedra in South Africa. 1st description in a child with bamboo hair, pili torti and congenital erythroderma ichthyosiforme].
- Follicular mucinosis in association with Sezary syndrome
- Alopecia Universalis Associated with Cutaneous T Cell Lymphoma
- 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
- Omenn syndrome in a 10-month-old male with athymia and VACTERL association
- An unusual case of increased hair pigmentation in previously grey-white hair
- [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
- Stanozolol in the Treatment of Pityriasis Rubra Pilaris