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Research 30 of 788
- Dental Management in a 7-year-old Child with Ichthyosis Vulgaris: A Rare Case Report
- Ichthyosis vulgaris involving the scalp area affected by androgenetic alopecia.
- Ichthyosis
- 155 Exploring perceived quality of life in middle- to old-aged patients with inherited ichthyosis: a qualitative study
- Symmetrical acrokeratoderma: A peculiar entity in China? Clinicopathologic and immunopathologic study of 34 new cases
- Dermatological aspects of the S2k guidelines on Down syndrome in childhood and adolescence
- FilaggrinHigh melanomas exhibit active FGFR and allergic signatures with impaired GNA14 and Th1 signatures
- Presentations of Cutaneous Disease in Various Skin Pigmentations: Keratosis Pilaris
- Keratosis Pilaris Is a Keratinization of Hair Follicles
- Disorders of Keratinization
- Genetics
- Chemotherapy of psoriasis and other skin disorders with oral retinoids
- Viva questions from the IJDVL
- Ichthyosis in Unani Medicine: A Comprehensive Review of Disorders of Cornification and their Modern Dermatological Correlates
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- The value of trichoscopy in the differential diagnosis of scalp lesions in pemphigus vulgaris and pemphigus foliaceus
- Management of congenital ichthyoses: European guidelines of care, part two
- NETHERTON'S SYNDROME AND ICHTHYOSIS LINEARIS CIRCUMFLEXA
- Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders
- Ichthyosis and Trichothiodystrophy: the Tay and PIBI(D)S Syndromes
- 0952 Spatial transcriptomics reveal compartmentalized dysregulation of lipid metabolism in acne vulgaris
- 305 Overlaps between inflammatory dermatoses and ichthyoses: need for novel therapeutic approaches
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Azelaic Acid: Mechanisms of Action and Clinical Applications
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Common Dermatologic Disorders in Down Syndrome: Systematic Review
- Ichthyosis with confetti: a rare diagnosis and treatment plan
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- First Symposium of Ichthyosis Experts
- Ichthyoses