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- Acquired ichthyosis, alopecia and loss of hair pigment associated with leiomyosarcoma.
- Acquired ichthyosis, alopecia and loss of hair pigment associated with leiomyosarcoma
- Ichthyosis in Unani Medicine: A Comprehensive Review of Disorders of Cornification and their Modern Dermatological Correlates
- The skin landscape in diabetes mellitus. Focus on dermocosmetic management
- Skin Manifestations of Hypothyroidism-A Clinical Study
- Diffuse plate-like sheets of desquamation
- Circle Hairs in a Patient with Multiple Myeloma
- Ichthyosis
- Dental Management in a 7-year-old Child with Ichthyosis Vulgaris: A Rare Case Report
- Disorders of Keratinization
- [Cutaneous manifestations of malabsorption diseases (author's transl)].
- Management of congenital ichthyoses: European guidelines of care, part two
- Acquired hypertrichosis lanuginosa: Case report and review of the literature
- Hair Shaft Fracture in a Young Athlete: A Rare Case Report of Acquired Trichorrhexis Nodosa
- Disorders of hair in children
- CLINICAL AND LABORATORY EVALUATION OF AIDS TRICHOPATHY
- Skin manifestations of endocrine diseases
- Symmetrical acrokeratoderma: A peculiar entity in China? Clinicopathologic and immunopathologic study of 34 new cases
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Trichodystrophies: A hair-raising differential diagnosis
- The spectrum of nephrocutaneous diseases and associations
- Cutaneous Syndromes Produced as Side Effects of Triparanol Therapy
- A STUDY ON CUTANEOUS MANIFESTATIONS OF HYPOTHYROIDISM IN A TERTIARY HOSPITAL IN SOUTH INDIA
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Oral Retinoids in Dermatology
- Common Dermatologic Disorders in Down Syndrome: Systematic Review
- A case of acquired trichorrhexis nodosa after applying new hair spray
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines